1. The document describes several types of hepatitis viruses including Hepatitis A, B, C, D, E, and G.
2. It provides details on their structure, mode of transmission, incubation period, potential for chronic infection, treatment options, and methods of prevention.
3. Key differences between the viruses involve whether they have an envelope, their nucleic acid composition, and their potential to cause acute versus chronic infection.
1. The document describes several types of hepatitis viruses including Hepatitis A, B, C, D, E, and G.
2. It provides details on their structure, mode of transmission, incubation period, potential for chronic infection, treatment options, and methods of prevention.
3. Key differences between the viruses involve whether they have an envelope, their nucleic acid composition, and their potential to cause acute versus chronic infection.
1. The document describes several types of hepatitis viruses including Hepatitis A, B, C, D, E, and G.
2. It provides details on their structure, mode of transmission, incubation period, potential for chronic infection, treatment options, and methods of prevention.
3. Key differences between the viruses involve whether they have an envelope, their nucleic acid composition, and their potential to cause acute versus chronic infection.
Family Picornavirus Hepadnaviridae Flavivirus Deltavirus Calcivirus Flaviviridae
Hepatitis A Hepatitis B Hepatitis C Hepatitis D Hepatitis E Hepatitis G
Envelope Non-enveloped/ Naked Enveloped Enveloped Enveloped Defective virus (delta virus) --> req. HBV for replication --> forms ribozyme intermed. during replication Noneveloped/ naked Enveloped DNA/RNA (+) ssRNA Partially circular dsDNA Reverse transcribed & integrated into host chromosome (+) ssRNA circular ssRNA HBV envelope HDV core (+) ssRNA (+) ssRNA Source/ Transmission Fecal/Oral***** (shellfish/ polluted water) [Parenteral spread] High: blood, serum, wound exudates Moderate: semen, vaginal fluid, saliva Low: urine, feces, sweat, tears, breask milk [Parenteral spread] -Perinatal transmission --> only if mom HCV-RNA (+) at delivery --> 6% infection rate, higher if HIV+, role of viral titer unclear --> no assoc. w/ delivery method or breastfeeding --> infected infants do well -Sexual transmission --> MSM no higher risk vs. heterosexuals --> Low prevalence amoung long-term partners --> M to F transmission more efficient --> Efficiency low (factors unknown) --> Accounts for 15-20% of acute & chronic infections [increased risk for infection] --> Ever injected illegal drugs --> Intranasal cocaine use --> Received clotting factors made before '87 --> Received blood/organs before '92 --> Ever had chronic HD --> Evidence of liver dz [Parenteral spread] Fecally contaminated water Minimal person to person Parenteral Tattoos Clinical Manifestations INCUBATION: Long (6 wk.- 6 month) < 5 yoa -Asymptomatic at first -60% will be chronic******* Adults: Usually Symptomatic, LESS chronic (5%) 80% of infants born to infected mother get HBV***** Mortality = 0.8% in acute illness Hepatocellular carcinoma INCUBATION: Long (2 - 26 wks) Acute infection (20%)- Mild anicteric (NO JAUNDICE) Chronic (80%) Of the Chronic cases- Cirrhosis in 20% -Way more Cirrhosis than HBV Rarely Fulminant Hepatitis Infected infants do well (unlike HBV) -Chronic/ severe hepatitis RARE in them Other presentations: Cryoglobulinemia (IgM precipitates in cold temps) Porphyria cutanea tarda, Aplastic anemia (BM stops) INCUBATION: Long (6 wks - 6 months) Worsening of HBV -Leads to Fulminant Cirrhosis (40% Coinfection (both at same time) Severe acute disease Does NOT go chronic Superinfection (one after the other) Get Chronic HDV High risk of Severe Chronic Liver Disease Incubation: ~40 days (1.5 month) No chronic disease Similar to HAV High mortality in pregnant**** -20% DIE Similar to Hep C Histopathology Ground-glass cytoplasm of hepatocytes****** Hepatocellular necrosis Fibrosis & Cirrhosis Portal and lobular inflammation Portal dense lymphocyte infiltrate w/ follicle forming Lobular inflammation Patchy lobar Steatosis Kuppfer cell hyperplasia Cholestasis- blocking of biliary tree --> jaundice Fibrosis & Cirrhosis Mnemonic: Hep D for Defective !"#$%&%&' )&*+'"' INCUBATION: 1 month (2-3 weeks) -No carrier state or chronic dz -Mortality 0.1% -Immunity lifelong Epidemiology 1.2 million carriers in U.S. 70% - 90% in Asia, Pacific islands, Middle east Factors Promoting Chronic HCV Increased alcohol intake- 7X likely****** Age >40 years when get infected HIV co-infection Male Other infections (ex: HBV) Note: not so much Occupational transmission 15 million cases in world. Italy, middle east, Africa. Endemic in developing countries (India, Asia, Africa, Mexico) Lab Diagnosis Anti-HAV Ig = exposed Anti-HAV IgM = recently vaccinated Immunostaining of HBcAg or HBsAg AA HBV surface antigen (HBsAg): (outer surface envelope) -Infected/carrier HBV core antigen (HBcAg): (core protein) -NO DETECTION/ TEST, don't order HBV e antigen (HBeAg): (DNA polymerase) -Means highly infectious due to active viral replication CHRONIC HBV: NEVER develop anti-HBs (ab to surface ag) Anti-HCV enzyme immunoassay (EIA) or ELISA -Screen for infected, chronic cases Recombinant immunoblot assay (RIBA) -Needed to confirm infection, chronic case HCV RT-PCR -For active infection to determine viral load Anti-HDV IgM Need to test Hep B also Anti-HEV Ig = exposed Anti-HEV IgM -use for Acute Infection Treatment No treatment available/ needed Interferon alpha 2B x 48 wks Entecavir or Tenofovir if resistance Tenofovir/Emtricitabine- if co-HIV -Assess for biochemical evidence of CLD -Assess for severity of dz & possible tx, according to current practice guidelines --> 30-40% sustained response to antiviral combo therapy (IFN alpha, Ribavirin) -6 Genotypes, 1 most common & hardest to treat -Ribavirin & IFN alpha-2b & Telapravir or Bocepivir (if Genotype I) No treatment available Can give HBV vaccine to help prevent No treatment available/ needed Post-exposure IgG prophylaxis?? Prevention Routine childhood vaccine Who needs vaccine: Travelers, gay men, drug users, chronic liver dz Immunization of infants required (@ 0-, 1-, 6- mo) -Also give to susceptible groups healthcare workers, sexual contacts of HBV carriers -Vaccinate vs. Hep A -Limit or abstain from alcohol NO immunization Give HBV though Ensure safe drinking water Only eat pealable fruit Don't eat uncooked shellfish Notes: Gotten from oysters and pools Only 1.8% transmitted after needle stick -Test for anti-HCV on source -If source positive: Test Anti-HCV & LFTs -Get baseline of both tests -Anti-HCV & LFTs @ 4- 6 mo., or PCR @ 4-6 wk. -Confirm all anti-HCV with RIBA Defective (needs HBV for replication) Envelope= Hep B RNA= Hep D -Can only infect in someone already infected by Hep B. Clinical signs of hepatitis: cirrhosis, jaundice, ascites, splenomegaly, elevated liver enzymes (transaminases), anemia, leukopenia, thrombocytopenia, liver damage, portal hypertension