The Immune Response of Prolactin and the Induction of Tumor Necrosis Factor (TNF) in Iraqi Patients Infected with Hepatitis C Virus.

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1 The Immune Response of Prolactin and the Induction of Tumor Necrosis Factor (TNF) in Iraqi Patients Infected with Hepatitis C Virus. Prof. Hedef Dhafir El-Yassin (MRSC, Ph.D, Post Doctorate) Department of Biochemistry, College of Medicine, University of Baghdad. Rana A. Hadi M.B.Ch. B. Candidate for the fellowship of the Iraqi Board for Medical Specialization in Pathology/ Clinical Chemistry

2 Prof. Dr. Hedef Dhafir El-Yassin 2016 Viral Hepatitis Type C is a serious public health challenge throughout the world and remain to be the major causes of chronic hepatitis. During the 80s, Iraq had low endemicity among blood donors. However its prevalence is now increased with high rate of mortality.

3 Hepatitis C is a contagious viral disease caused by hepatitis C virus.

4 Brett D. Lindenbach and charles M. Rice described a hypothesis for the detailed molecular mechanism of HCV infection in an article entitled : The ins and outs of hepatitis C virus entry and assembly, published in Nature Reviews Microbiology : Volume: 11, Pages:688 700 :(2013)

5 Prof. Dr. Hedef Dhafir El-Yassin 2016 Berlin/ Germany

6 (step 1) Hepatitis C virus (HCV) lipoviral particles (LVPs) attach to the cell surface by interacting with: heparan sulphate proteoglycans (HSPGs), low-density-lipoprotein receptor (LDLR) and scavenger receptor class B member 1 (SRB1). SRB1 might delipidate HCV-associated lipoproteins and induces conformational changes in the E2 glycoprotein, exposing the CD81-binding site

7 (step 2) Prof. Dr. Hedef Dhafir El-Yassin 2016 Interaction of E2 with CD81 then activates signal transduction through epidermal growth factor receptor (EGFR) and HRAS, as well as through RHO GTPases. (step 3) These signaling events promote lateral movement of HCV CD81 complexes to sites of cell cell contact.

8 (step 4) Interaction of CD81 with claudin 1 (CLDN1), and HCV internalization via clathrin-mediated endocytosis. (step 5) The low ph of the endosomal compartment induces HCV fusion.

9 Many cases (two third) could go through undiagnosed because they might be asymptomatic. However the rest one-third of people initially infected with hepatitis C develop symptoms and are more likely to be treatment efficiently with antiviral drugs.

10

11 Those infected but asymptomatic will develop to chronic HCV and will initiate a broad-based immune response. (adaptive and innate immune response).

12 Prof. Dr. Hedef Dhafir El-Yassin 2016 Berlin/ Germany

13 It is clinically important 1. to differentiate : incident HCV infections from chronic infections 2. and to identify primary infections that are asymptomatic.

14 Occasional occurrences of acute exacerbation in chronic infection, will complicate decisions regarding whom to treat with the suitable treatment.(1)

15 Hepatitis C virus-related chronic hepatitis is associated with various immunological disorders example: Immuno-endocrine Cytokines Anti-tissue antibodies

16 Interaction of these molecules might trigger a cascade of reaction that will be involved in the progression of the disease. And/or might influence the effect of drug of choice that is used for the management of the disease.

17 Prof. Dr. Hedef Dhafir El-Yassin 2016 Berlin/ Germany Aim of the study: To evaluate the role of the immunoendocrine system in the pathogenesis of chronic hepatitis c, by measuring serum prolactin and tumor necrosis factor-alpha.

18 Subjects involved in the study were selected from Gastrointestinal Hospital in Baghdad, Iraq. During the period from July 2014 to September 2014. A written consent was taken from each.

19 Subjects n.= 81 Patients: n=61 Median Age =34.8 yrs. n=20 Control: Median Age= 34.6 yrs. Male Female Male Female n.= 29 n.= 32 n. =10 n.= 10

20 All patients had chronic hepatitis C virus and were on interferon alpha therapy. All of them were positive for HCV RNA by means of polymerase chain reaction.

21 Diagnostic algorithm for hepatitis C Anti HCV ELISA Reactive.elevated transaminases.immuno compromised HCV RNA Non reactive No further investigation +ve -ve Consider retesting in six months

22 Blood samples were collected between (9.00a.m- 12.00p.m). The blood was allowed to clot in plain tube for 30-45 minutes at room temperature. Sera were obtained by centrifugation of the collected blood and then stored in plain tubes at -20 c. ELISA technique was used to measure (TNF and Prolactin)

23 Parameter Serum prolactin (ng/ml) Groups Mean ± SEM Patients 12.54 2.9 Control s 11.50 2.7

24 The role of PRL in the immune reactions is stimulating; its presence significantly increases the ability of the immune cells to proliferate and produce cytokines such as TNF-alpha(2)

25 Recent studies suggest that prolactin is important both for normal liver growth and for regenerating the liver after part of it is removed, with extra prolactin providing a boost for repair mechanisms. Consequently, enhancing prolactin levels could provide a way to improve regeneration when the liver becomes damaged or diseased with viruses, or after surgery.(3)

26 Parameter Serum TNF-alpha (ng/ml) Groups Mean ± SEM Patients 65.57 7.03x x10-3 10-3 Controls 41.52 1.86x x10-3 10-3

27 Prof. Dr. Hedef Dhafir El-Yassin 2016 Berlin/ Germany HCV infection enhances TNF-α-induced cell death by suppressing nuclear factor NF-κB activation through the action of core, (non structural HCV ) NS4B, and NS5B. This mechanism may contribute to immunemediated liver injury in HCV infection. (4)

28 Prof. Dr. Hedef Dhafir El-Yassin 2016 70 60 50 40 30 20 10 0 65.57 41.5 11.5 12.54 Control Patients Prolactin ng/ml ng/ml10-3 TNF x

29 Prof. Dr. Hedef Dhafir El-Yassin 2016 Berlin/ Germany ng/ml TNF x10-3 85 80 75 70 65 60 55 50 45 Correlation between serum prolactin and TNF in pateints group 41.57x + 1.912y = 0.317= ² R 40 5 7 9 11 13 15 17 19 21 23 Prolactin ng/ml

30 Parameter Serum ASMA Groups Patients Controls % 65.57 +ve 34.43 % -ve 100% -ve

31 The result agrees with Clifford et al in their study they reviewed the presence of autoimmune markers in sera of chronic hepatitis C patients. Their study showed that treatment with interferon alfa (IFN-alpha) will exacerbate autoimmune hepatitis. (5) The pathogenesis of autoimmune hepatitis due to medications is not clear.

32 Recommendations from an expert panel Aiming for treatment optimization by filling some of the gaps of the current guidelines, a group of Italian experts, experienced on treatment of HCV infection, met in Stresa in February 2016. The summary of all the considerations arising from this two-day meeting and the final statements are reported in Digestive and Liver Disease Journal June 2016 [Epub ahead of print]

33 Treatment of chronic HCV (CHC) has been revolutionized in the last few years by the introduction of highly effective and well tolerated direct acting antiviral agents (DAAs) able to achieve >90% rates of sustained virological response (SVR) in many groups of patients, including those previously excluded from interferon-based regimens. For such reason interferon-free regimens are now the treatments of choice for all patients. Successful anti-hcv treatment can stop liver disease progression and can solve the HCV-related extra hepatic manifestations, eventually reducing both liver-related and overall mortality.

34 Conclusions: Chronic hepatitis C is associated with an immunological abnormality mainly represented by tumor necrosis factor-alpha and prolactine. This might shed a light of the type of therapy and drug of choice when managing the disease.

35 References: 1. C.H. Chen, and C.-S. Changchien. Is it possible to diagnose acute hepatitis C virus (HCV) infection by a rising anti-hcv titer rather than by seroconversion? J. Viral Hepat. 11:563 570, 2004 2. Fojtíková M 1, Cerná M, Pavelka K. A review of the effects of prolactin hormone and cytokine on the development and pathogenesis of autoimmune diseases.vnitr Lek.56(5):402-13,.2010 [Article in Czech]. 3. CarmenC, Moreno B, Maite G. Prolactin promotes normal liver growth survival and regeneration in rodents. American Physiological Society; 10:1152, 2012. 4. Park J, Kang W, Ryu SW.Hepatitis C virus infection enhances TNFα-induced cell death via suppression of NF-Κb.Journal of Hepatology; 56(3):831-40, 2012 5. Clifford BD,Donahue D,Smith L.High prevalence of serological markers of autoimmunity in patients with chronic hepatitis C. Journal of Hepatology; 21(3):613, 1995 6. Craxì A, Perno CF, Viganò M, Ceccherini-Silberstein F, Petta S; AdHoc (Advancing Hepatitis C for the Optimization of Cure) From current status to optimization of HCV treatment: Recommendations from an expert panel. Dig Liver Dis. 2016 Jun

36 Any questions? Thank You