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Hepatitis viruses zamberi.tripod/index

Hepatitis viruses http://zamberi.tripod.com/index. Dr Zamberi Sekawi BSc (Med), MD (UKM), MPath (Microbiol), AM (M’sia) Clinical Microbiologist Faculty of Medicine & Health Sciences University Putra Malaysia. VIRAL HEPATITIS. Hepatitis A virus Hepatitis B virus Hepatitis C virus

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Hepatitis viruses zamberi.tripod/index

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  1. Hepatitis viruses http://zamberi.tripod.com/index Dr Zamberi Sekawi BSc (Med), MD (UKM), MPath (Microbiol), AM (M’sia) Clinical Microbiologist Faculty of Medicine & Health Sciences University Putra Malaysia

  2. VIRAL HEPATITIS Hepatitis A virus Hepatitis B virus Hepatitis C virus Hepatitis D virus Hepatitis E virus Hepatitis G virus Future: ? Hepatitis H virus ? Hepatitis I virus ? Hepatitis J virus Etc…

  3. HEPATITIS A VIRUS Picornaviridae Hepatovirus Non-envelope, single-stranded RNA, positive sense. Only one serotype.

  4. Incubation period: 2 – 6 weeks Transmission: • faecal-oral • food/water • blood product Associated with poor personal hygiene and overcrowding. More symptomatic in adults.

  5. Symptoms Constitutional symptoms of anorexia, nausea and vomiting, fatigue, malaise, arthralgias, myalgias, headache, photophobia, pharyngitis, cough, and coryza may precede the onset of jaundice by 1 to 2 weeks. Nausea, vomiting, and anorexia are frequently associated with alterations in olfaction and taste. Dark urine and clay-coloured stools may be present. Tender hepatomegaly.

  6. Fulminant hepatitis occurs in elderly and patients with underlying liver disease. Presentation: Severe jaundice, neurological changes, coagulopathy, renal failure, cardiopulmonary failure. High mortality rate.

  7. Lab diagnosis Serology: IgM positive: recent hepatitis A IgG positive: past hepatitis A

  8. Prevention Passive immunisation Anti-HAV preparation. Used in post-exposure prophylaxis. Active immunisation Formalin-inactivated vaccine. Approved for use in those > 2 years old. Recommended to selected groups of people, e.g. travellers, food handlers, laboratory workers, etc. Adults: 0, 6 - 12 months Children: 0, 1, 6 – 12 months

  9. HEPATITIS B VIRUS Hepadnavirus double-stranded DNA HBsAg -- Anti-HBs HBeAg -- Anti-HBe HBcAg -- Anti-HBc

  10. 350 million chronic carriers world-wide. Malaysia:  5% Prevalence is highest in China, Africa (Sub-Sahara), South East Asia and among Eskimos. Transmission: 1. Blood product 2. Vertical transmission (predominant in endemic areas) 3. Sexual transmission 4. Intravenous drug abuse

  11. 10% 65% 25% Subclinical infection Acute Chronic Carrier <1% Fulminant Hepatitis Cirrhosis Hepatocellular Carcinoma Lifelong Immunity Death Adults

  12. Acute hepatitis B (1) Incubation period: 1 – 6 months.HBsAg and HBeAg start to increase during this period. Patient is infectious. (2) Acute symptoms:Jaundice, fever, nausea, right hypochondriac pain.ALT reaches high level. 

  13. (3) The appearance of anti-HBe and anti-HBc antibodies. HBeAg disappears. Symptoms resolving. (4) Window period‘Window period’= period between disappearance of detectable HBsAg and appearance of detectable anti-HBs by standard laboratory test.

  14. (5) Patient in convalescent state. Anti-HBs, the protective antibody becomes detectable. (6) Years later. IgM anti-HBc disappears in 3 – 12 months. IgG anti-HBc and persist for life.

  15. Acute Hepatitis B

  16. Chronic Hepatitis B The presence of HBsAg in serum for 6 months or longer after initial detection. High risk groups: 1. Neonates 2. immunocompromised host Majority is asymptomatic. Minority experiences only mild and intermittent fatigue.

  17. Chronic Hepatitis B (1) Immune-tolerant phase High viral replication. The host is able to tolerate the presence of the virus.

  18. (2) Immune-clearance phase. Low viral replication.Patient will enter this phase when tolerance to HBV break down (about 15 – 35 years later).Host actively tries to eradicate virus. Therefore, ALT are raised.There were increasing production of anti-HBe.Most of liver damage happens during this time, leading to cirrhosis.The longer the duration of this phase, the greater the liver damage. Hence the risk of liver cancer is high.

  19. (3) Latent infection phase Patient enters this phase once HBV-infected cells are destroyed by the immune system.Active replication cease and HBeAg disappear.ALT normal. Anti-HBe positive. HBsAg is still present. ‘Healthy carrier’.Anti-HBs is never produced.

  20. Chronic hepatitis B model

  21. Patient will have cirrhosis and eventually die of hepatocellular carcinoma (HCC). Risk of acquiring HCC from chronic hepatitis B is 98 times of the normal population.

  22. Lab investigations Serology: 1. HBsAg: Presence of virus (acute or chronic) 2. HBeAg: Active replication of HBV. 3. Anti-HBs: Immunity to HBV either by natural infection or vaccination. 4. Anti-HBe: Low viral replication. 5. Anti-HBc: Ongoing or previous HBV infection depending on IgM or IgG.

  23. AcuteConvaChrPost-vac HBsAg + - + - HBeAg + - +/- - Anti-HBe - + -/+ - Anti-HBc IgM + - - - Anti-HBc IgG + + + - Anti-HBs - + - +

  24. Treatment Acute hepatitis Supportive. Chronic hepatitis Aim: to help the body to eradicate the virus. (during the second phase). Recommended for patients with: • persistent levels of ALT in serum • detectable levels of HBsAg, HBeAg and HBV DNA in serum • liver biopsy suggesting chronic hepatitis and compensated liver disease.

  25. Presence of anti-HBe and normal ALT (third phase) will indicate the treatment is effective. 1.  interferon 2. Pegylated  interferon 3. Lamivudine 4. Adefovir 5. Entecavir

  26. Prevention Three main strategies: 1. behaviour modification 2. active immunoprophylaxis 3. passive immunoprophylaxis Active immunisation has been very successful. Standard regimen: 0, 1 and 6 months Highly efficacious (85 to 95% seroconversion). Immunocompromised patients respond poorly to the vaccine.

  27. Passive immunoprophylaxis is used in: 1. neonates born to HBsAg-positive mothers. Anti-HBs immunoglobulins should be given immediately after delivery together with the recombinant HBV vaccine. (90% protected) 2. after needlestick exposure. 3. after sexual exposure. 4. after liver transplantations in patients who are HBsAg-positive pretransplantation.

  28. HEPATITIS C VIRUS Flavivirus single-stranded RNA, positive sense 6 genotypes (1 through 6).

  29. Hepatitis C virus mutates very rapidly. Therefore, the production of protective antibody is short-lived. Vaccine production is very difficult. Worldwide incidence: 1 – 2% Higher rates in Eastern Europe and Africa (especially Egypt). Genotypes  1a :North and South America, Australia 1b :North America, Europe, Japan 2 :North America, West and Southern Europe 3 :Australia, Southern Asia 4 :Egypt, Central Africa 6 :Asia

  30. Transmission: 1. Blood borne (especially blood transfusion) 2. Injection-drug abuse 3. Vertical transmission (uncommon) 4. Multiple sexual partners Incubation period: 2 weeks Associated with extrahepatic manifestation. E.g. mixed cryoglobulinaemia and membranoproliferative glomerulonephritis.

  31. 80 - 95% 5 – 20% Persistance infection (Chronic Hepatitis C) Clearance Cirrhosis Hepatocellular carcinoma DEATH Primary Hepatitis C 20 years

  32. Laboratory diagnosis 1. Screening: Serology. e.g. ELISA. 2. Confirmation: Immunoblot assay e.g. RIBA, LIA Genome detection. e.g. PCR.

  33. Treatment and prevention Treatment: a)IFN  monotherapy Sustained response rate for: 6-month therapy = 10 – 20% 12 – 18-month therapy = 15 – 30% b)Combination IFN  and ribavirin Sustained response rate:  40% (Sustained response: normal ALT  undetectable HCV RNA 6 months after completion of therapy)

  34. Interferon therapy is indicated in patients who are at the greatest risk for progression to cirrhosis: 1. Persistently elevated ALT > 6 months. 2.Detectable serum HCV RNA by a qualitative or quantitative assay. 3.Liver biopsy = grade 2 or 3 fibrosis. 4.Moderate degrees of liver inflammation and necrosis. No vaccine is available.

  35. HEPATITIS D VIRUS a.k.a. delta hepatitis agent. Defective RNA virus, requires HBV for its replication.

  36. Worldwide distribution with endemicity in the Mediterranean countries. HDV can either: • infect a person simultaneously with HBV (coinfection) or • superinfect a person already infected with HBV (superinfection). Duration of HDV infection is determined by duration of HBV infection. Serology No specific treatment. Prevention by giving HBV vaccine.

  37. HEPATITIS E VIRUS Non-envelope, single-stranded RNA, positive sense. World wide distribution. Causes acute hepatitis. High mortality among pregnant women.

  38. HEPATITIS G VIRUS Also known as GBV-C. Genome: single-stranded RNA, positive sense. 25% similar to hepatitis C. Transmission: 1.Blood transfusion 2.Injecting drug users Hepatic damage appears to be mild or absent. Role as a causative agent is still questionable.

  39. Enquiries: 03 – 8946 8459 zamberi@medic.upm.edu.my szamberi@yahoo.com http://zamberi.tripod.com/index

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