Gepatonin in Brief
Gepatonin now pass registration at the Pharmacological Committee of the Ministry of
Health and Social Affairs of Georgia.
Gepatonin has passed preclinical and clinical trials in following organizations:
The Kiev Medical Institute named after Bogomolts, Department Infectious Diseases, Kiev, Ukraine.
Medical Center Diseases "Dobrobutt", Department Infectious Diseases, Kiev, Ukraine.
Clinical and Experimental Research Institute of Tbilisi State Medical University;
Medical & Biological Scientific Research Centre – Company <<Alexis>>;
Laboratory of Cell Signal Mechanisms of the I.Paladin Institute of Biochemistry at
Ukrainian Medical Academy;
Medical Research Institute of Physical Chemistry at the Ministry of Healthcare of
Pharmacological Department of the Medical University of Russian Federation;
Fuji Memorial Institute of the Preclinical Research, Bivako/Japan;
Tokushima Otsuka Immunology Research Institute, Japan;
Tokushima Institute of New Drug Research and Safety Evaluation, Japan;
Gepatonin is recommended for the treatment of cirrhosis, hepatitis-A,B,C and over liver disorders.
Clinical trials show that use of the Gepatonin in the treatment of patients with chronic hepatitis C possesses rather high efficiency in treatment of patients with virus hepatitis C disease:
Unpleasant feelings in the right hypochondrium disappeared, the general condition considerably improved.
Expressed positive dynamics of indicators of ALT, AST, thymol test, GGT, the general bilirubin is obvious.
Application of GA- Gepatonin is expedient at patients with chronic hepatitis C which have contraindications to carrying out PVT.
Gepatonin action does not depend on a genotype of a virus of hepatitis C, but to some extent depends on a stage of phibrosis of liver: clinical and biochemical improvement was more expressed at phibrosis F2 and F3.
Most likely Gepatonin can be applied to radical treatment of chronic hepatitis C , practically without contraindications. It is not excluded that Gepatonin in a combination with PVT can be applied in treatment not only for not respondents, but also persons with an adverse genotype of IL28 v, at which efficiency of standard PVT within 20-25%.
In 2 months after completion of treatment the PCR-test for HCV remained negative with 60% of patients.
Molecular Mechanism of the Gepatonin Anti-Hepatitis C Action.
Getting (penetration) into the body hepatitis C virus causes suppression of the immune system by inhibiting Interferon’s (IFN) production by mononuclear immune cells. Interferon’s inhibit protein synthesis within the infected cells and reduce viral replication in host cells. Inhibition protein synthesis destroys both the virus and infected host cells and restricts the entry of the virus in neighboring cells. Another function of interferon’s, such as interferon-γ (INF-γ), is to directly activate mononuclear immune cells, such as T-killer, NK-cells, macrophages and others.
Activated cells release cell lytic cytotoxins perforin, granzymes, and granulysin and trigger apoptosis, programmed cell death of the hepatitis C virus infected target cells. Viral spread also limit by increasing p53 activity, which kills virus-infected cells by promoting apoptosis. Release of IFN-ƴ from cells is also induced by cytokines, such as interleukin 1, interleukin 2, interleukin
12; tumor necrosis factor can also enhance interferon-ƴ production. During prolonged HCV infection many complex processes play critical roles in the development of liver damage. One of these processes includes enhanced production of free radicals, causing liver oxidative stress, increase HCV disease activity in chronic hepatitis, causes liver injury leading to fibrosis and eventually hepatocellular carcinoma.
The results of pre and clinical trials of the medical preparation Gepatonin, allows to submit a scheme of the molecular mechanisms Gepatonin anti-hepatitis C virus-action, which leads to the high efficiency of the Gepatonin treatment of patients with chronic hepatitis C virus disease.
In the treatment of chronic hepatitis C using Gepatonin crossing an inactive form of the disease occurs from 1 to 7 treatments for all patients. In addition, the transition to an inactive form has a permanent effect. In patients treated with the control exerted over four years and in
95% of cases (for lack of provoking factor) activation was not found.
After four courses of treatment recommended control analysis of the presence of virus (PCR). When negative results every six months during the two years it is necessary to operate the control PCR.
If after four treatments PCR showed the presence of virus, hepatitis should be continued, and
after seven treatments once again make PCR analysis.
The end result of the total elimination of the virus occurs in 60% of cases.
The amount of therapy depends on the severity of the person and the dynamics of treatment.
When using the preparation Gepatonin in most cases achieved regression of disease as evidenced by the fact that the preparation Gepatonin has very strong hepatoprotektorna characteristics and affects the recovery process of the exchange of substances (protein, lipid,
and carbohydrate). Regardless of the etiology of cirrhosis (viral, alcoholic, autoimmune)
improve the condition occurs in 91% of cases.
The amount of therapy depends on the severity of the person and the dynamics of treatment.
CTL- T-killer cells , NK-cell- natural killer cell, MF- macrophage, DK-dendrites’ cell, NF- neutrophils, Cytotoxin-granzymes, and granulysin, Fas L - is a homotrimeric type II CTL an NK- cell transmembrane protein. Fas L recognize, interact and bind with Fas (death receptor), which spans the membrane of the cancer or infected "target" cells. This high specifically interaction between Fas L and Fas surface receptors usually leads to apoptosis, or cell death.
· Gepatonin activates mononuclear cells, cytotoxic-T cells (T-killer cell) s, T-helper, Natural killer cells (NK-cells), macrophages, neutrophils. Activated cells release infected cell lytic perforin and cytotoxin-granzymes, and granulysin and trigger apoptosis - programmed cell death of the hepatitis C virus infected target cells. A second way to induce apoptosis is
via cell-surface interactions between the T-killer cells, NK-cells cells and the infected cells. The final result is apoptosis of the hepatitis C virus infected target cells.
· Gepatonin activates production of Tumor Necrosis Factor (TNF-α), which induce release Interferon-ƴ. Both cytokines TNF-α and IFN-ƴ kills virus-infected cells by promoting apoptosis of the hepatitis C virus infected target cells.
· Gepatonin with high Anti-oxidant activity neutralizes free radicals and reduces the oxygen with two unpaired electrons, inhibit oxygen stress and decrease chronic HCV disease activity in patients.
Anti-inflammatory and antifibrotic effects of plant regulatory peptides in patients with steatohepatitis and cirrhosis. Opportunities of primary liver cancer prevention.
Anatolyy Pechinka¹, Levan Kakliani², Zurab Gogitidze³, Sergii Konovalenko, Iryna Miroshnychenko
1 - Shupyk NMAPE, Department of Infectious Diseases, Kyiv, Ukraine
2 - Department of Internal Medicine, University Hospital of Tbilisi, Georgia
3 – Regul Medical Information Center
4 - RE Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology, Kyiv, Ukraine
5 - Kyiv City Center for Radiation Protection of Kyiv Population from the Consequences of the Chornobyl Catastrophe
The pathogenesis of steatohepatitis, which develops on the background of non-alcoholic fatty liver disease and may be the cause of liver cirrhosis, is considered in the article. Also, the paper focuses on the prospects of using peptide drugs for the treatment of liver cirrhosis. The study found that the preparation of plant regulatory peptides GEPATONIN has pronounced hepatoprotective, anti-inflammatory and anti-fibrotic effects, which is confirmed by the elastometry data of the shear wave. The results of this work indicate that the use of the drug GEPATONIN was accompanied not only by the normalization of the inflammatory panel of the liver and triglycerides, but also by a likely decrease in the level of glypican-3 - the main factor that causes the development of primary liver cancer. Gene protector and immunocorrector harmonizing metabolic processes in the liver, as well as suppressing inflammation and preventing excessive output of hepatocytes in apoptosis, has a positive effect on the prognosis of the disease. Reduced expression of glypican-3 in patients in the study group indicates that GEPATONIN is able to control the level of pro-oncogenic trigger proteins, thus reducing the risk of primary liver cancer.
Key words: steatohepatitis, cirrhosis, glypican-3, GEPATONIN, hepatocellular carcinoma.
Introduction. Non-alcoholic fatty liver disease (NAFLD) is a disease that results from excessive fat accumulation (mainly triglycerides) in the form of steatosis in the liver in people who do not consume alcohol in amounts capable of causing liver damage. [1,2]
NAFLD and non-alcoholic steatohepatitis (NASH) are more common in women aged 40-60 years, but there are reports of this type of pathology in younger patients. NAFLD is a type of liver steatosis or fatty hepatosis that occurs in people who do not abuse alcohol and is most commonly associated with insulin resistance and metabolic syndrome. The term "NAFLD" has several synonyms: non-alcoholic liver steatosis, fatty liver, fatty infiltration of hepatocytes. [3,5,7].
One of the most characteristic phenomena in this disease is theaccumulation of fat in the functioning tissue of the liver. In the future, it leads to the replacement of this tissue with adipose tissue, which eventually causes the development of chronic inflammation. Isolated liver steatosis is a relatively benign condition with minimal risk of progression to more severe liver disease. [4,6,8].
The development of inflammatory processes on the background of fatty dystrophy leads to damage hepatocytes and the progress of non-alcoholic, or metabolic, steatohepatitis, which is one of the stages of NAFLD, and steatohepatitis gradually leads to liver cirrhosis. [9,10]. This mechanism also works with viral, toxic (alcohol) lesions as an additional damaging factor.
Non-alcoholic fatty liver disease occupies one of the leading positions among diffuse liver diseases. The relevance of the study of NAFLD is due to
both the prevalence of the disease and the risk of developing cirrhosis and hepatocellular carcinoma (HCC) (Figure 1).
The proportion of patients with NAFLD in the adult population ranges from
6.3% to 33% with a median of 20% in the global population. In some countries, the incidence is 46% . The progression of the disease also increases the risk of liver cirrhosis and liver failure. Studies have shown that a quarter (27%) of patients with NAFLD develop fibrosis within 9 years, and one in five (19%) have cirrhosis of varying degrees of severity [12,13].
It is established that the stage of fibrosis, and not the severity of inflammation, is the prognostic factor that determines the subsequent fate of patients and the likelihood of complications. In this regard, it is important to look for predictors of progression of liver fibrosis to individualize therapy and follow- up of the patient. At the present stage, it seems interesting to study gene
polymorphisms in the development or progression of diseases.
The G-allele of the PNPLA3 gene is positively correlated with the triglyceride content of liver tissue, and its loss of activity may be directly related to
inflammation of the liver tissue. Concerning the association of PNPLA3 with the development and progression of liver fibrosis in histologically confirmed NAFLD, regardless of obesity, diabetes mellitus and steatosis, convincing data have also been presented . Participation of this gene in liver cirrhosis formation and transformation in HCC has been proved , regardless of external factors (obesity, alcohol consumption). The polymorphism of the PNPLA3 / 148M gene is today an independent genetic factor for the development and progression of NAFLD and non-alcoholic steatohepatitis.
Figure.1 Scheme of progression of non-alcoholic fatty liver disease.
A. Accumulation of lipid (triglyceride) droplets inside hepatocytes causes steatosis. Steatosis associated with inflammation, cell death and fibrosis progresses and non-alcoholic
steatohepatitis develops, which can turn into cirrhosis. People with cirrhosis have an
increased risk of developing hepatocellular carcinoma.
B. Histological sections showing the normal state of the liver, steatosis, steatohepatitis and cirrhosis. Collagen fibers are colored in blue by the Masson method. A portal triad (PT) consisting of a hepatic artery, a portal vein, a bile duct and a central vein (CV) is shown .
Glypican-3 (GPC3), an oncofetal proteoglycan, attaches to the cell membrane, usually found in the liver of the fetus, but not in the healthy liver of the adult. However, in patients with HCC GPC3 is overexpressed and its expression predicts poor prognosis. Studies have shown that GPC3 functions in the progression of HCC by binding to molecules such as Wnt signaling proteins and growth factors. [17-19]
According to D. Baumhoer et al. , positive expression of glypican-3 is also observed in individual high-grade dysplastic nodules, indicating their carcinogenic orientation. Elevation of glypican-3 is also considered as a prognostic factor for HCC in patients with cirrhosis. Glypican can enhance mRNA expression of HCC-related genes and participate in the neoplastic process in the cirrhotic liver. Therefore, GPC3 can serve as a precursor biomarker in liver cirrhosis. [21,22]
Moreover, GPC3 was used as a target for molecular imaging and therapeutic intervention in HCC.  Magnetic resonance imaging focused on GPC3, positron emission tomography and near-infrared tomography for early detection of HCC have been investigated, various GPC3 immunotherapeutic protocols have been developed, including the use of humanized anti-cytotoxic DNA / cytotoxic treatments , immunotoxin therapy, and genetic therapy. [24,25]
GEPATONINis the first gene protector and immunocorrector based on plant regulatory peptides to be used in clinical practice. It is known that GEPATONINpeptides, due to their relatively small size (15-98 kDa), can affect not only membrane receptors but also penetrate cells through membrane pores. This enables them to interact with intracellular structures: regulatory peptides and genes, ligands and enzymes. Studies have also demonstrated that GEPATONINpeptides are intracellularly capable of altering the active potential of participants in the regulatory cascades: mRNA-associated proteins, caspases, protein kinases, prointerleukins, interleukins, and the like.
The history of the discovery and study of the immunotropic and gene- protective properties of GEPATONINis set out in professor George Alexidze's monograph “ GEPATONIN. New Immunotherapy and Anticancer Drug”, which was released in 2014 in the USA - Lambert Academic Publishing. Feb 12, 2014).
The uniqueness of GEPATONINis that plant peptides under conditions of reduced antitumor immunity due to aggressive tumor activity or after antitumor
chemotherapy restore immune surveillance and promote apoptosis of cancer cells. 
In opposite conditions, that is, in conditions of hyperproduction of immunocompetent molecules in inflammatory processes, in particular in the liver and kidneys (in hepatitis, cirrhosis, nephritis), plant peptides are able to reduce the intensity of peptide-peptide interactions and prevent undesirable damage to healthy сells. 
This paradox can be explained by the evolutionarily formed properties of regulatory peptides - self-assembling and the natural intention for harmonization.
Aim of research. In order to study the hepatoprotective, anti-inflammatory and antifibrotic action of GEPATONIN, we formed two groups of patients diagnosed with steatohepatitis, liver cirrhosis.
Materials and methods
Based on the Department of Therapy of the University Clinic of Tbilisi
(Georgia), from 2016 to 2019 experience in the use of GEPATONINwas obtained in
34 patients (25 women and 9 men aged 44 to 65 years) with steatohepatitis (23) and cirrhosis liver (11). To study the hepatoprotective, anti-inflammatory and anti-fibrotic properties of GEPATONIN, a control group of patients - C (N = 34) was recruited.
The study group received the following treatment: ademetionine 400 mg 2 times a day tablets orally, verospiron capsules 50 mg 2 times a day, triamterene with hydrochlorothiazide (25 mg + 12.5 mg tablets) orally and GA-
40 on a pulse schedule - 400 μg of solution of regulatory peptides per day injected intramuscularly for 28 days, total of 6 courses for 28 days with breaks in 1 week.
The control group received therapy according to the scheme: ademetionin
400 mg 2 times a day tablets orally, verospiron capsules 50 mg 2 times a day, triamterene with hydrochlorothiazide (tablets 25 mg + 12.5 mg) orally.
We monitored ALT, AST, GGT, C-reactive peptide, and triglyceride levels for treatment at 35, 75, 105, 140, 175, and 210 days of follow-up. Such distribution of control points is conditioned by the scheme of therapy in the study group: 28 days is the introduction of GEPATONIN, then 7 days of break - and control for 35 days, then another 28 days of therapy, 7 days of break - and control for 70 days, etc. As a marker of the risk of primary liver cancer, we used the expression level of glypican-3 (GPC-3).
The level of fibrosis was controlled by ultrasound-shear elastometry. The study group had 11 patients with liver cirrhosis in stage F4 on a METAVIR scale with different levels of fibrosis. Indicators were monitored before treatment and after treatment.
Results and Discussion
The study groups were comparable in the pre-treatment phase (p> 0.05). Clinical observations show that in the study group in the first month of therapy there was a tendency to normalize ALT, AST and other biochemical indicators of liver inflammation. Gradually decreased serum triglyceride levels. (Table 1). Similar dynamics of biochemical parameters were recorded in the control group, especially in the first 2 months of observation, but on the 105th and
175th day, the AST marker level increased slightly - to an average of 54.3 IU / l and 49.5 IU / l, respectively. , which formed a statistically significant difference compared to the study group (p <0.05). A statistically significant difference
between the ALT groups is formed from 105 days of observation, and the AST
level from 35 days is maintained until the end of the study (p <0.05).
With quite positive dynamics of decrease in inflammatory marker GGT in the control group, on day 210, there was a slight increase in it from an average of 21.8 to 34.7 IU / l (p <0.05 when compared between groups). Also, in the control group, expression of the C-reactive peptide after a marked decrease from the level of 9.1 IU / ml to 4.9 IU / ml increased again at the sixth control point to 7.2 IU / ml (p <0.05). (Table 2) It should be noted that there were no such increases in the study group and the levels of AST, ALT, GGT and C- reactive peptide remained within the normal range throughout the observation period from the second control point.
Figure 2. Level of glypican-3 in patients during treatment.
Equally interesting was the assessment of glypican-3 (GPC3) protein expression in patients in the study and control groups. In the first five weeks after the start of the treatment protocol, there was a slight decrease in serum GPC3 concentration from 39.9 - 41.4 to 33.6 - 38.3 ng / ml in both observation groups. However, at the third point of control, on the 70th day from the start of pulse therapy, the average expression of GPC3 in patients in the study group showed a sharp decrease to 17.4 ng / ml (p <0.05). This trend persisted - on day 105 of the treatment course, the level of GPC3 in the patients in the study group dropped to 7.1 ng / ml and remained relatively low throughout the
observation period. At the same time, GPC3 expression reached the level of
26.6 ng / ml on day 140 of the treatment protocol in patients of the control group, and after 5 weeks it increased significantly again - up to 33.8 ng / ml. At the final reference point, GPC3 activity increased again to 37.7 ng / ml, almost
returning to baseline. A statistically significant difference between the groups
(p <0.05) begins to form after 35 days of observation.
All 11 patients with cirrhosis in the study group had a statistically significant decrease in liver fibrosis. In 3 of them, to the F3 level on the METAVIR scale, and in the rest - to the initial F4 level: from 35.3 kPa on average, there was a decrease to 12.7 kPa.
It can be reasonably assumed that the gene protector and immunocorrector GEPATONIN, by harmonizing metabolic processes in the liver, as well as suppressing inflammation and preventing excessive hepatocytes exit into apoptosis, have a positive effect on the prognosis of the disease. Reduced expression of glypican-3 in patients in the study group indicates that GEPATONIN with a high probability is capable of controlling the level of pro-oncogenic trigger proteins, thus reducing the risk of primary liver cancer.
The results of this work indicate that the use of the drug GEPATONIN was accompanied not only by the normalization of the inflammatory panel of the liver and triglycerides, but also a likely decrease in the level of glypican-3.
The results obtained confirm that the preparation of plant regulatory peptides GEPATONIN has pronounced hepatoprotective, anti-inflammatory and anti- fibrotic effects, which is confirmed by the elastometry data of the shear wave.
Against the background of complex treatment, not only was the gradual regression of the clinical symptoms of the disease, but there was a significant improvement in the general condition and quality of life of patients.
At this stage, the inclusion of GEPATONIN in the treatment regimens of steatohepatitis and cirrhosis of the liver is quite reasonable, especially since this drug is able to significantly reduce the risk of hepatocellular carcinoma and significantly reduce the degree of liver fibrosis. Such properties make it possible to consider GEPATONIN as a potential drug for delaying or even avoiding the terminal stage of liver cirrhosis, in which indications for transplantation arise.
Clinical Trials GEPATONIN on Patients with Chronic Hepatitis C Viruses Diseases
P. V. Doroshchenko
Chief physician of “Dobrobut”
doctor of the highest category,
EXPERIENCE OF APPLICATION OF THE PREPARATION GEPATONIN
AT VIRUS HEPATITIS C
In modern conditions the liver constantly is exposed to various influences from environment. The range of exogenous toxic factors extends: alcohol, xenobiotics (artificial dyes and preservatives in foodstuff, medicines with toxic effects), excessive loading fats in a diet, and also the infections caused by hepatotropic viruses, parasitic invasions. Relevance of a problem of virus hepatitis C (HCV) is caused by high prevalence HCV infection (to 6% on the globe) and sufficient percent of synchronization of a HCV infection (from 33 to 92% infected, depending on a virus HCV genotype), making the main share among all chronic defeats of a liver. On infection frequency virus hepatitis C is on the first place among all infections which are transmitting through blood: in the world there are about 300 million HCV infected. According to modern data, only in the USA there are registered 3 million people infected with HCV. From them 8–10 thousand people die annually and the majority of transplantations of a liver is carried out to the patients sick with HCV. In Europe the number of infected HCV makes to 2% from all population.
Due to the difficulty of creation of a specific vaccine against the hepatitis C, the virus which was characterized by high mutational variability of hepatitis C and ability "to escape" from immune supervision, the indicator of incidence of HCV can treble by 2010 (according to World Health Organization (WHO data). The problem is aggravated with that for a long time at the majority of HCV infected the asymptomatic course of a disease takes place. The latent course of a disease allows to consider that the percent of revealed HCV sick is much lower, than the index of infection of the population.
Now HCV infected are most often young people, mainly men at the age of 20 years, 38–40% from them catch at intravenous administration of drugs. Approximately at a half of patients the way of infection does not manage to be established. The main way of a HCV transfer is parenteral (transfusions, an organ transplantation from the infected donors, intravenous administration of drugs). Infection is possible sexually, the child from mother and also at household contacts.
The genome of a virus of hepatitis C contains the unary thread of RNA coding intracellular synthesis of structural and nonstructural proteins. Infection by a RNA-genomic virus of hepatitis C is one of the leading reasons of incidence and mortality around the world, causing a wide range of defeats of a liver from an asymptomatic carriage to a terminal stage of a disease. As a result of a long persistence of a virus of hepatitis C in an organism the chronic disfunction of a liver leading to development as cirrhosis, and a hepatocellurar cancer develops.
Pathogenesis of a HCV infection is connected with direct cytotoxic action of a virus and violations of immunological reactions that leads to injury of a liver and other bodies. Morphologically there develop inflammatory and necrotic and degenerate pathological processes of a parenchyma and biliary tract system of a liver. Both in the present, and in the future chronic hepatitis C remains extremely important problem for health care around the world. Despite measures for decrease in prevalence of a HCV infection, at huge number of earlier infected patients disease progressing in cirrhosis and a hepatocellular carcinoma will proceed. The progressing course of chronic hepatitis C with cirrhosis formation (from 2,4 to 24%) and development of primary cancer of a liver – a hepatocellular carcinoma (at 5%) assumes application in tactics of treatment of a HCV infection not only antiviral therapy, but also hepatoprotective preparations.
The main objective of treatment of patients with chronic hepatitis C is achievement of elimination of a virus from an organism, the prevention of progressing of specific pathological process and disease recurrence, and also improvement of a functional condition of a liver. Now therapy of a HCV infection is provided with application of antiviral preparations (IF-s interferons, analogs of nucleosides), having direct ethiological and pathogenetic value. Correction of functional insufficiency of a liver as a result of hepatotoxic effects of a virus of hepatitis C demands application of preparations of the hepatoprotective property allowing not only to improve its function, but also to cause a reduction of fibrogenesis.
At diffusion diseases of a liver, as well as at any pathological process, a number of the general actions is shown. A strict confinement to bed the majority of patients do not need, except for the expressed signs of an aggravation (distinct cholestasisi, increase of activity of Alaninaminotransaminase more than by 4–5 times in blood serum in comparison with norm). The diet structure at patients is quite wide. Alcohol has to be completely excluded, in the period of an aggravation smoked products, fried dishes, refractory fats are limited. At the same time fats are natural cholagogic means and therefore their share in a daily diet (oil, margarine) has to make about 35% from the general caloric content. The amount of protein (vegetable and animal) is recommended within physiological norm (80–100 g/days), and carbohydrates – 400 - 500 g/days.
At progressing hepatic insufficiency the daily diet of protein decreases to 40 g/days. The amount of table salt at a liquid delay (portal hypertensia) is limited to 2 g/days. Existence of cholestasis significantly limits digestion of fat-soluble vitamins (A, D, E). Besides, at diffusion diseases of a liver the need for vitamins C, B6, B12 is increased, that it is necessary to consider when developing an individual diet.
Long time ethiotrpic therapy of chronic hepatitis and cirrhosis was complicated. It was connected with that there were no enough data on the reasons of development of these diseases. Only in 1994 the leading hepatologists offered to consider one of the basic classification principles at diffusion diseases of a liver the ethological. Now it is established that a leading ethological factor in development of chronic hepatitis and cirrhosis are hepatotrophic viruses (B, C, D, G) with a parenteral way of their transfer. The reason of autoimmune hepatitis as independent disease is still insufficiently clear. The mechanism of its development is connected with reactions in the immune system, connected with development of autoantiboides (against microsomal anti-genes of cells of a liver, their nucleus and the proteins specific to a liver). Abuse of alcohol is considered as the possible reason of an acute hepatitis, fatty dystrophy of a liver and cirrhosis. Drugs and some medicinal substances if can have independent etiological value in development of chronic diffusion diseases of a liver, it is rather rare. It is important to note that alcohol, drugs and a number of medicines can promote development of a virus infection and assist thus to progressing of pathological process in a liver. Existence of markers of viruses in serum of blood is not always combined with manifestations of pathological changes in a liver. Probably so-called "carriage" of a virus at which clinical signs and morphological changes in a liver are absent. At considerable number of patients (their about 70%) with chronic hepatitis the pathological process connected with infection by a virus, as though "stiffens" for long term years and more) at the level of the minimum activity without a tendency to progressing. In the recent past such favorable course of a disease was regarded as chronic персистирующий hepatitis. And at last, at a number of patients the illness from the very beginning gains the moderated and expressed activity of process, rather quickly and steadily progresses and in some years is transformed to cirrhosis, and at some part from them transforms to a hepatocellular carcinoma. Earlier such option of a disease with a progressing current was called active (aggressive) hepatitis.
The Chronic Hepatitis (CH) irrespective of an ethiological form can have various degree of expressiveness a syndrome of cholestasis, and at CH alcoholic, cholestatic and choleangiogenic this syndrome is the leader and meets in 11–55% of cases. As clinical manifestation of this syndrome is the skin itch, however it is found only in 10–40% of patients. Emergence of jaundice at a syndrome of cholestasis makes heavier the general condition of the patient. From the preparations influencing certain links of pathogenesis, now are widely used ademethionin and ursodesoxicholic acid. However these preparations are made abroad and from the economic point of view are available to not all patients. At chronic hepatitis suffers the liver parenhim therefore it is necessary to direct treatment on restoration of its cells. In this regard in the scheme of treatement of chronic hepatitis it is necessary to include medicines which unite the concept "hepatoprotectors". This is a group of medicines with the various mechanisms of action directed on normalization of functions of a liver, potentiation of reparative and regenerative processes, restoration of a homeostasis and increase of stability of body to action of pathogenic factors.
In the presence at the patient of markers of viruses in combination with clinical signs of activity of process anti-virus therapy is shown. Thus creation of optimum conditions for carrying out such treatment is important. It provides a complete elimination of alcohol, restriction of medicines. Now the main ethiotropic means for treatment of virus diffusion defeats of a liver is interferon. For treatment of virus hepatitises the greatest distribution has interferon, both received of culture of leukocytes, and recombinant, created by means of genetic engineering (an intron A, Ropheron A, Reapheron, Realdiron). Now it is considered expedient to combine purpose of interferon with other preparations. There is the sufficient clinical experience, allowing to recommend in 15–20 days prior to purpose of interferon glucocorticoids (Prednisolon of 20-30 mg per day). Purpose of adsorbents, the means normalizing structure of microflora of intestines, vitamins C by microcells, pancreatic fermental preparations is as well recommended.
Work Purpose. To study efficiency and safety of the immunomodulating preparation GEPATONIN in treatment of virus hepatitis C.
Materials and Methods. GEPATONIN– represents immunomodulating complex of biologically active peptides received of ecologicaly pure plant material in a form of peptide type lyophilized powder. After carrying out biochemical researches about quantitative and qualitative structure it was revealed that the preparation contains some hundred small peptides with a molecular weight of 10-50 kD. For definition of structure the method of a highly effective liquid chromatography (HPLC) with the subsequent tandem mass spectrometry of masses with use of LTQ FT ICR of a spectrometer of masses (Hybrid-2D-Linear Quadrupole Ion Trap, Fourier Transform Ion Cyclotron Resonance Mass Spectrometer) (Thermo Electron Corp) was used. It should be noted that the majority of the endogenous peptides present at a human body possessing biological activity (cytokines, hormones, antibodies, dephensins, alarmins ), have just quantitative aminoacid structure from 10 to 50 and respectively low molecular weight. This fact is explained by that small molecules are easier transported in organism tissues, and also have a high tropism to ligand interaction with membrane receptors. Also it should be noted that these small active peptides work in very small nano - and pico-concentration.
In preliminary preclinical and clinical tests on volunteers there is established ability of the immunotherapeutic preparation GEPATONIN to restore in blood quantitative and functional indices B and T of cellular systems of immunity, in particular, T-helper cells, T-cytotoxic cells, T-killers (NK), macrophages, granulocytes; to normalize ratio of T-helper and T-supressor cells, to induce production of cytokines, including interferon - gamma; to restore functional activity of stem haemopoetic cells; to normalize level of the content in blood of leukocytes, erythrocytes, neutrophils, platelets, lymphocytes and other uniform elements of blood.
The preclinical assessment of safety which is carried out according to requirements "The guide to experimental (preclinical) studying of new pharmacological substances" (M, 2000), with application of toxicological, patomorfological, biochemical, hematologic methods, did not reveal any essential differences of indicators of experimental groups of animals from control group that testifies to lack of toxic influence of medicine GEPATONIN in studied doses.
Due to these properties of the medical preparation GEPATONIN, we counted expedient to include immunomodulating GEPATONIN complex in the scheme of therapy of chronic virus hepatitis C and to study its efficiency and safety.
In research of efficiency and safety of application of GEPATONIN in complex therapy of chronic hepatitis C 30 patients were included: 26 men and 4 women aged from 21 up to 48 years; 21 patients had a diagnosis: virus hepatitis C, stage 1b; 9 patients have a virus hepatitis C, a stage 3а. During treatment patients received from 3 to 8 courses GEPATONIN, the quantity of courses of therapy depended on expressiveness of positive dynamics of clinical disease manifestations. The diagnosis of a HCV infection was confirmed by means of PCR-tests. During therapy there was carried out PCR-diagnostics after each course of application of GEPATONIN, and also the remote control in 2 months after treatment. Before an initiation of treatment and after each course of application of GEPATONIN, control of the following indicators was exercised: Alaninaminotranspherase, Aspartataminotranspherase (ALT, АSТ), thymol test, GGT, general bilirubin.
Results and Discussion. During carrying out treatment by the preparation GEPATONINat 1 patient the PCR-test became negative after 3 courses (3,3%), at 9 patients – after 4 courses (30%), at 6 patients – after 5 courses (20%), at 6 patients – after 6 courses (20%), at 5 patients – after 7 courses (16,6%) and at 2 patients – after 8 courses (6,6%). In 2 months after negative PCR-test for HCV at 18(60%) patients the negative result remained. (Tab. 44)
Biochemical parameters in patients in dynamics in patients in the study group.
* - statistically significant difference between the levels of the study group and control group (p <0.05, Mann-Whitney test). Δ is the dynamics of the indicator relative to the previous period with the estimation of the statistical significance of the dynamics according to the Wilcoxon criterion (* -p <0.05
Biochemical parameters in patients in dynamics in patients in the control group.
Δ is the dynamics of the indicator relative to the previous period with the estimation of the statistical significance of the dynamics according to the Wilcoxon criterion (* -p <0.05).
Dynamics of results of PCR-tests, (+) – positive, (-) the negative.
Dynamics of indicators of Alaninaminotranspherase (ALT)
Dynamics of indicators of АСТ.
Dynamics of thymol test and general bilirubin.
Dynamics of indicators of GGT.
Conclusions. Thus, as a result of the carried-out work we established that the preparation GEPATONIN possesses rather high efficiency in treatment of viral hepatitis C: in 2 months after completion of treatment the PCR-test for HCV remained negative with 60% of patients. Expressed positive dynamics of indicators of ALT, ACT (ALT, АSТ), thymol test, GGT, the general bilirubin is obvious. At the majority of patients, especially after 4-5 courses of therapy, intoxication manifestations decreased, unpleasant feelings in the right hypochondrium (hypochondria) disappeared, the general condition considerably improved.
Estimating the obtained data, especially positive dynamics of biochemical indicators, and also obvious improvement of a condition of patients, we can recommend GEPATONINfor wide use in treatment of viral hepatitis C.
Clinical Trials GEPATONIN on Patients with Chronic Hepatitis C Viruses Diseases
The preparation GEPATONINin basic therapy of patients by virus hepatitis’s
P. V. Doroshchenko
Chief physician of MDC "Dobrobut"
doctor of higher category
Among all gepatotropny viruses the most dangerous and insidious is the hepatitis C (HC) owing to the high choriogenic potential, the erased flow, complicating modern diagnostics of this disease and serious consequences of infection. According to different authors, in the world of HC it is infected from 170 million to 2 billion people and rates of its distribution increase. Today it is a question of a pandemic of this disease which on scales and number of the infected people exceeds distribution of HIV infection to 4 – 5 times.
Now in treatment of the HC chronic forms will make significant progress: at application of standard antiviral therapy (PVT) by preparations of interferon and ribavirin it was succeeded to reach the resistant virologic reply.
However a number of the questions connected with carrying out standard PVT, remain open. First of all it is impossibility in some cases of its applications owing to available serious contraindications at the patient (bronchial asthma, critical levels of hemoglobin, leukocytes, platelets, etc.). Also arising serious undesirable phenomena in the course of carrying out standard PVT stay to be a problem, which force it to interrupt or to reduce a dose of applied preparations that inevitably affects results of therapy. At last, an important factor in our country is the cost of therapy and commitment of patients to it (it is known that many patients and even doctors negatively treat traditional methods of treatment of HC). All above-mentioned sets a task of search of alternative methods of therapy of the HC chronic forms which have smaller efficiency in respect of achievement of the resistant virologic reply for national authorities of health care, however favorably influence various links of pathogenesis HC that leads to improvement of clinical-biochemical indicators at patients, and, probably, to achievement of the virologic reply. It should be noted that the specified methods of nonspecific therapy do not replace standard PVT, however can improve at a certain stage a condition of patients up to disappearance of available contraindications to standard PVT, or to be alternative treatment to patients for whom PVT is impossible to prescribe.
It is known that the normal cell of a liver has the program of proliferation causing its reproduction, and the program of apoptosis. Destiny of a cell, so, of body and an organism as a whole, depend on that how, in what interaction these programs work. But if mechanisms of proliferation are well studied and found the final conceptual statement in works on molecular biology of the last 15 years, regulation of apoptosis is still studied insufficiently. However at many conditions of violation of this program become defining for the course of a disease. For a very long time value of programmed death of cells was underestimated, however recently the interest to mechanisms of its realization has been much increased, and this problem became one of very much most really intensively studied areas of biology. Today it is known that violation of control of cellular death conducts to shifts of a homeostasis and development of various pathological conditions.
Apoptosis has the major role both in physiological, and in pathological conditions in view of the fact that both suppression, and inadequate strengthening of apoptosis conducts to pathological changes of bodies and tissues. While truly excess activation of apoptosis, observed, in particular, at infection of cells of a liver by hepatotrophic viruses, causes destruction of hepatic tissue, weakening of apoptosis death of cells (caused, for example, as a mutation of the gene coding proapoptogenic (proapoptogenic protein р53) serves one of the most important factors of carcinogenesis. Researches of the last years showed that pathogenesis of many diseases of a person is connected to inability of cells to be exposed to apoptosis, such as, at a cancer, a leukosis, autoimmune diseases and virus infections. In the experimental works which have been carried out including on hepatocytes, the increase in free radicals in a cell, to concentration of free intracellular calcium, activation of proteases in process apoptosis is shown. At virus hepatitis apoptosis can be result of direct influence of a virus, and the immunomediated reaction. In researches of the last years it is shown that at HC processes of apoptosis are proceeded insufficiently actively.
Considering all the aforesaid, recently the increasing attention is paid to development of the medicines influencing processes of apoptosis. In works of the last years the role of polypeptides in regulation of these processes is shown. Now vegetable and animal polypeptides find the increasing application in medicine. Their main mechanism of action – an induction of cellular apoptosis, stimulation mielopoesis, increase of quantity of antibody synthesizing cells.
The inductor of apoptosis the polypeptide GEPATONIN complex was developed in the early nineties in the Medico-Biological Research and Production Center “Alexis” (Tbilisi, Georgia).
Materials and methods. In clinic of infectious diseases of Ukraine Medical University under supervision there were 55 patients with chronic HC at different stages of fibrosis in a liver. Men were 29 (52,7%), women – 26 (47,3%). All patient conducted full clinical-laboratory examination with definition of level serumal transaminases, bilirubin, the general protein, proteinaceous fractions, immunograms, also molecular and biological research with definition of a genotype of a virus of hepatitis C and quantitative definition of virus loading (ME/ml.). For an assessment of efficiency of therapy clinical criteria were used (weakness, appetite, feeling of heaviness in hypochondrium, etc.), and also dynamics of decrease in activity of ALT and virologic loading.
For assessment of stage of fibrosis of liver by the standardized system METAVIR to all patients was carried out a transdermal biopsy of a liver in surgery clinics under УЗ-control by means of the device SDU-600A "Shimadzu", equipped linearly- trapezoidal sensor 3.5Мгц and a lateral punctшщтфд nozzle. Receiving a column of tissue for histologic research was carried out by means of needles of "Tru-Sut" 16G. The biopsy was carried out in a ribs ribson the axillary line under local anesthesia. Coloring of bioptates was carried out by hematoxylin-eosin and picrofuxin in a Van Gizon method.
All patients were divided into two groups. 1 group included 36 patients with chronic hepatitis C (CHC), receiving as nonspecific therapy of GEPATONIN, 2 group (control) included 27 patients with the chronic HC, receiving treatment basic therapy: enterosorbents, hepatoprotectors (Ursofalk). Distribution of patients depending on a stage of fibrosis of the liver is presented on the following charts.
Fig. 6. Distribution of patients of 1 group depending on a stage of phibrosis of liver.
As we see from the chart, patients with fibrosis F2 and F3 – 23 prevailed (63,9%).
On the following chart there are presented patients of the 2nd group depending on a stage of phibrosis of liver.
Fig. 7. Distribution of patients of 2nd group depending on a stage of phibrosis of liver, %.
Thus, groups are almost comparable by number of patients to different stages of phibrosis of liver.
At 21 (58,3%) patients of 1 group was defined 1 genotype of a virus, at 15 (41,7%) – for virus genotype.
At 21 (55,6%) patients of 1 group was defined 1 genotype of a virus, at 12 (44,4%) – 3 – for virus genotype.
Distribution of virus loading at patients both groups is presented on the following charts.
Fig.8. Specific weight of patients of 1 group with various virus loading depending on a virus genotype, %.
Fig. 9. Specific weight of patients of 2nd group with various virus loading depending on a virus genotype, %.
As we see from the chart, in all groups high virus loading prevailed at patients with 1 genotype of a virus.
The clinical picture had nonspecific character and was characterized by weakness (at fibrosis F1 this symptom was not observed), with decrease in appetite, at expressed fibrosis (F3, F4) at part of patients appeared a skin itch (5 patients of group 1 and 3 of patients of group 2). All these symptoms did not depend on the genotype of a virus and virus loading. All patients of 1 group received as GEPATONIN therapy. The preparation was injected hypodermically once a day into fixed time. The dose was defined according to the weight of the patient and made 2 mcg/kg of weight of a body (2 mkg = 0,01 ml). The duration of one course of therapy made 21 injections. In total patients received 5 courses of therapy. The interval between courses made 21 days.
Character of the main accompanying pathology and some extra hepatic manifestations at patients with HC (group 1 and 2).
As we see from the table, at patients had defeats of a gastrointestinal path, and also autoimmune thyroiditis prevailed.
Results and their discussion. In the 1st group of patients already at the middle of the first course of treatment noticeable improvement of a clinical picture of a disease was noted, and more considerably it was observed at patients with the expressed stages of phibrosis of liver: appetite improved, weakness decreased, the skin itch considerably decreased. The last symptom at patients with defeats of a liver is especially unpleasant, delivers the mass of subjective unpleasant feelings by the sick and is extremely difficult in treatment. As a result patients lose appetite, have sleeplessness, become irritable, negatively treat various methods of treatment owing to their small impact on unpleasant subjective feelings. All this complicates psychological contact with patients. At application of the preparation GEPATONIN for all 5 patients during already first course of treatment this symptom either is noticeable decreased, became incidental, or absolutely disappeared.
In the analysis of laboratory indicators reliable decrease in activity of ALT in the 1st group of patients, in comparison with control is revealed, at 9 (25%) patients activity of enzyme by the end of treatment was normalized.
Dynamics of decrease in activity of transaminases at the patients of both groups is presented on the following chart.
Fig.10. Dynamics of decrease in activity of ALT at sick chronic hepatitis C (CHC).
As we see from the figure, activity of ALT tended to decrease in both groups, however in the 1st group its fast decrease was noted more and at part of patients normalization of activity of ALT was observed.
Dynamics of virus loading at the patients of both groups before the carried-out treatment are presented in the following drawings.
Fig.11. Dynamics of virus loading at patients of the 1st group before the carried-out treatment.
Dynamics of virus loading at patients of control group before the carried-out treatment. In the analysis of dynamics of virus loading at the patients of the both groups the following regularities came to light: at patients of the 1st group decrease in virus loading at 8 (22,2%) patients was noted, and more expressed its dynamics was observed at patients with initially low virus loading (< 600 000 МЕ/ml), than at the patients with high virus loading (> 600 000 МЕ/ml, and at 7 patients with initial low virus loading at the end of a course of treatment it decreased to not defined level. At patients of control group decrease in virus loading during treatment it was observed at 2 (13,3%) patients with initially low loading and at one patient with high virus loading.
Feature of biochemical and virologic answers to therapy of GEPATONIN is increase of activity of ALT at 29 (80,6%) patients and increase in virus loading at 22 (74,1%) patients. Possibly, it is connected with strengthening of the phenomena of apotosis of liver. However already by the end of the second course of therapy at the majority of patients it was noted natural decrease in the above indicators which reached the maximum at 19 (52,8%) patients by the end of a third course, and at 17 (47,2%) patients – by the end of the fifth course.
Use of the inductor of apotosis GEPATONIN at patients HC leads to clinical-biochemical remission at a number of patients. Unstable virologic remission was reached at part of patients with initially low virus loading (less than 600 000 ME/MLl).
Application of vegetable polypeptide GEPATONIN is expedient at patients with chronic hepatitis C (CHC) which have contraindications to carrying out PVT.
Action of a preparation does not depend on a genotype of a virus of hepatitis C, but to some extent depends on a stage of fibrosis of liver: clinical and biochemical improvement was more expressed at fibrosis F2 and F3.
Clinical Trials GEPATONIN on Patients with Chronic Hepatitis C Viruses Diseases
Associate professor of infectious diseases
Candidate of medicine science A.M Pechanka.
The Kiev Medical Institute named after Bogomolts
Office Infectious Diseases
Relevance of a problem of virus hepatitis C (HCV) is caused by high prevalence HCV infection (to 6% on the globe) and sufficient percent of synchronization of an HCV infection (from 33 to 92% infected, depending on a virus HCV genotype), making the main share among all chronic defeats of a liver. At infection frequency virus hepatitis C is on the first place among all infections which are transmitting through blood: in the world, there are about 300 million of HCV infected. According to modern data, only in the USA 3 million people infected with HCV are registered. From them 8–10 thousand people annually die, and the majority of transplantations of a liver are carried out to also HCV infected people. In Europe the number of infected HCV makes to 2% from all the population.
The main objective of treatment of patients with chronic hepatitis C is achievement of elimination of a virus from an organism, the prevention of progressing of specific process and disease recurrence, and also improvement of a functional condition of a liver. Now therapy of a HCV infection is provided with application of antiviral preparations (interferones, ribavirin), having direct ethiologic and pathogenetic value. Correction of functional insufficiency of a liver as a result of hepatotoxic effects of a virus of hepatitis C demands application of preparations of the hepatoprotective property allowing not only to improve its function, but also to cause a reduction of fibrogenesis. Besides, efficiency of double component therapy nevertheless wishes the best, averaging 50-60% at the most widespread 1 type of the virus НС Application of triple therapy (INF+Roferon+Boceprevir) about which they presently much speak, cardinally will not change number of not respondents and will be complicated with several difficulties:
• Very high cost of a preparation
• Heavy collateral reactions
• Reduction of number of not respondents by 30-40%
Thus, cost of treatment of not respondents becomes truly "diamond".
Practically the problem of the patients having contraindications for carrying out standard antiviral therapy (PVT) within existing preparations is not solved. And if to add not respondents, a number of sick people with НС-infections waiting for liver transplantation remains enormous.
So, it is possible to tell that the problem of treatment of hepatitis C is solved at best on a half. But also the other half demands attention.
Therefore small research concerning application of an immunomodulator of a phytogenesis of GEPATONIN for treatment of patients by chronic hepatitis C – first of all "not respondents" on standard PVT and persons with contraindications for treatment of standard PVT was conducted.
In preliminary preclinical and clinical tests on volunteers ability of the immunotherapeutic preparation GEPATONINto restore in blood quantitative and functional indices B and T of cellular systems of immunity, in particular, T-helper cells, T-cytotoxic cells, T-killers (NK), macrophages, granulocytes is established; to normalize ratio T-helper and T-supressorcells, to induce production cytokines, including interferon - gamma; to restore functional activity of stem haemopoetic cells; to normalize level of the content in blood of leukocytes, erythrocytes, neutrophils, platelets, lymphocytes and other uniform elements of blood. The major GEPATONIN property is also the induction of cellular apoptosis – one of the most important mechanisms of recovery.
Thanks to such properties of the preparation GEPATONIN, we counted expedient to include immunomodulating GEPATONIN complex in the scheme of therapy of chronic viral hepatitis C and to study its efficiency and safety. In the main group, in connection with restriction of quantity of a preparation and duration of treatment were included patients at a different stage of process – 1-4 stages of fibrosis and cirrhosis. Besides, at 2 patients with the 3rd genotype of a virus was carried out triple therapy: Pegasis 135/linear iterferon+kopegus+GEPATONINfor 14 weeks (3-4 courses). Application of the preparation GEPATONINhad under itself need to correct arising thrombocytopeny, a leykopeny, and also the arisen local allergy at injection of пегасиса (1 patient). The preparation showed moderate activity concerning a leykopenia and thrombocytopenia, but allowed to graduate treatments. At both patients the prompt virologic reply was received and duration of a course was reduced to 16 weeks, recurrence of a disease did not take place.
The preparation was prescribed in a usual mode from 3rd week of PVT when falling neutrophils to 420 and 480 neutrophils 1 mkl and platelets to 45 and 53 thousand. Against a preparation it was succeeded to achieve increase of neutrophils to 895 and 907 cells in 1 mkl and platelets to 76 and 73 thousand and to graduate treatments.
2 more patients with chronic hepatitis C (CHC) 1в genotype, received 9 courses of therapy of GEPATONIN. At one patient гетерозиготный IL28V type (probability of a successful conclusion of a course pegintron+INF+ribavirin – 40-50%) (pegintron +INF+ribavirine – 40-50%), at the second – an adverse genotype of IL28V (success of therapy pINF+ribavirin no more than 20-25%) was noted. Due to thrombocytopenia and a leukopenia from 3rd week GEPATONINis prescribed. At them it was not received the prompt virologic reply therefore decided to continue a course of GEPATONIN for 3 months. In 12 weeks the early virologic answer (PCR-negative) is received. Considering an intermediate and adverse genotype of IL28V, a course continued up to 9 months. Both patients who successfully finished PVT course, are under supervision: in 3 months after PVT, PCR termination negative. Once again we underline: so-called "problem" patients to whom standard PVT is not shown are taken in group or it was unsuccessful, a half of them was in a cirrhosis stage.
Characteristic of patients.
Age 53 years, male, diagnosis: chronic hepatitis of 1 genotype, a stage fibrosis F3, accompanying diseases: steatohepatitis alcoholic and not alcoholic, arterial hypertension of 2 st, chronic pancreatitis, calculous cholecystitis.
Course PVT pegasis 180 mkg +copegus for 24 weeks was unsuccessful: the virus again developed in blood after the 5th month, the course if infergen is stopped in 4 months because of heavy general collateral reactions.
Age 52 years, female, diagnosis: the chronic hepatitis C 3 a genotype, F3, accompanying
diseases: steatohepatitis not alcoholic, diabetes 2nd type, chronic
pancreatitis, chronic calculouse cholecystitis, menopause beginning. Unsuccessful course of combined (pegylated + simple + ribavirin).
Age 27 years, female. chronic hepatitis C 3 genotype, stage of phibrosis F1-2, accompanying diseases: chronic often reccurence pancreatitis. erythematous gastroduadenopatiya. Treatment Linear INF of 3 million every other day and 800 mg ribavirin daily for 24 weeks. Treatment transferred hard. On background of an exacerbation of pancreatitis. It was accompanied by a leukopenia and thrombocytopenia. Recurrence in 3 months after the course PVT termination.
Age 38 years, male, the cirrhosis of baking associated with the HCV-infection 1 genotype, F4 with phenomena of portal hypertensia. stage in on Chayld-Piyu, a syndrome of hypersplenismus and splenomegalia, varicose expansion of veins of a gullet of 2 st. Accompanying diseases: chronic pancreatitis, gastroduodenopatiya After metabolic and vascular preparation course PVT ( pegasis + kopegis ) is begun, which was stopped in 16 weeks due to the lack of the virologic answer both the expressed thrombocytopenia and a leykopeniya.
5. Age 48 years, male, the diagnosis chronic hepatitis of 1 genotype, a stage of phibrosis F3 accompanying diseases: steatohepatit alcoholic and not alcoholic, arterial hypertension of 2 st, chronic pancreatitis, obesity of 3 st. Before PVT was not carried out
6. Age 44 years, female, diagnosis: chronic hepatitis of 1 genotype, stage of phibrosis F4 + autoimmune hepatitis. PVT with simple IFN, was unsuccessful.
7. Age 32 years, male. Diagnosis: chronic hepatitis of 1 genotype, F4, portal hypertensia, varicose expansion of veins of a gullet of 3 st, ascites, hypersplenism syndrome , a stage B by Chayld-Piyu.
8. Age 17 years, male. diagnosis: chronic hepatitis B, HBsAg (+), anti-HBcor IgG (+), high virus loading, in the anamnesis in 3 years radical chemotherapy malignant tumor. Laser stimulation thymus was ineffective.
Under supervision there were 12 patients, from them 11 – sick with chronic hepatitis C (CHC) (3 – a cirrhosis stage), 1 – chronic hepatitis B (CHb), a stage of fibrosis F-2. To 4 patients therapy, IFN-+ribavirin+GEPATONIN combined from 3 weeks was carried out – they are discussed above.
At all patients receiving GEPATONIN, lack of collateral reactions was noted, and also during supervision, there was no aggravation accompanying a gastroduodenopathy, pancreatitis. If it used as a part of PVT, GEPATONIN partially stopped hematologic complications, about its influence on other complications of PVT it is difficult to speak.
At other 8 patients positive dynamics of activity of transferases and contradictory – virus loading was noted.
Dynamics of indicators of АLТ.
At a half of patients after the first course activity increase of transaminases was noted, thus at all gradual decrease in their activity was noted and only at 1(12,5%) they were almost normalized.
Dynamics of results of PCR-tests, (+) – positive, (-) negative.
(-) – PCR negative at the sensitivity of reaction to 200 copies /ml
(+/-) – the viremia decreased to 500 copies at sensitive reactions to 200 copies
* for the period of report writing the viremia given of the last control were absent, but in dynamics, the viremia considerably decreased
** only 3 courses due to the lack of preparation are conducted
Patients 1,3, 4,5, 8 continue supervision. Only patients 1, 3, 5 received the courses GEPATONIN lasting 8-9 months, 4 and 8 managed to receive only on 3 courses and further treatment was stopped due to the lack of preparation.
It is difficult to consider the result of the patient No. 6 positive as at control of a viremia high level of autoimmune indicators was at the same time noted – anti-nuclear antibodies exceeded norm almost by 6 times.
From the provided data of control of activity transaminases and viremia it is possible to draw such preliminary conclusions demanding to carry out full researches:
Obvious immunotrophy of the preparation to what activity increase of trans in an initiation of treatment and a gradual decrease in their activity in the course of treatment testifies.
Obvious antiviral efficiency was noted only at long treatment – 8-9 courses.
At long treatment decrease in the quantity of a virus is noted also, but during treatment at one patient, the virus did not disappear from the blood.
Most likely, GEPATONIN is a peculiar effect of an after-effect while to uncertain duration. In 3 cases the control made in 6 months and more (9 months – the patient No. 6) months showed disappearance or decrease in a titer of a virus to the definition level.
Now the patient No. 1 passes a virus control on test systems of the sensitivity of 50 copies/ml.
Conclusion: Most likely GEPATONIN can be applied to the radical treatment of PVT, practically without contraindications. It is not excluded that GEPATONINin a combination with PVT can be applied in treatment not only for not respondents, but also persons with an adverse genotype of IL28 v, at which efficiency of standard PVT within 20-25%.