BBV Flashcards

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1
Q

Discuss the features of Hepatitis B

A
  • Heoadnavirus -DNA
  • Immune reaction to the presence of the virus - infects hepatocytes
  • 6 genotypes A-F -High prevalence in SE Asia. subsaharan africa ect

Features: 6 week incubation period- 6months

  • Non-specific fever and malaise prodrome -50% infections asymptomatic
  • Chronic infection- cirrhosis , hepatocellular carcinoma
  • Antigen of Hep B= BHsAG - grossly overproduced so there is free antigen in the blood
  • HBeAg - another viral component
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2
Q

Describe the tolerogen effect of Hep B

A
  • E antigen is soluble and has a tolerogen effect (decreases the immune system)
  • Can cross the placenta and allows foetus immune system to recognise it as self antigen- causes clonal detection of lymphocytes recognising the E antigen
  • Leads to chronic infection- no immune response so virus won’t clear

Risk of chronic infection relates to age of infection - younger age= more likely

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3
Q

Describe the features of perinatal transmission of Hep B

A
  • E-antigen predicts the likelihood of transmission
  • Mother positive for HBsAG and HBeAG then 70-90% chance of infection
  • Positive for just HBsAG then less than 10%
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4
Q

What do these markers for Hepatitis b indicate

HBsAG
HB core antibody (IgG)
BH core antibody (IgM)
e antigen
Anti-HbsAg 
HBV DNA
A

HBsAg= current infection
HB core antibody IgG= past/ present infection (will still have this even if completely cured)
Hb core antibody IgM= Acute/ recent infection
E antigen= Highly infective, high grade infection
-Anti-HBsAg- Immunity (natural or vaccine)
-HBV DNA= measures response to treatment

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5
Q

What are the 2 types of HBV chronic infection

A
  • E-antigen positvie- high grade infection with increased risk of transmission- chronic acute hepatitis, cirrhosis and hepatocellular carcinoma likely
  • E-antigen negative - Low grade infection, low risk of onward transmission, nit likely to have clinical effects
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6
Q

Discuss the vaccine and treatment options for HBV

A
  • -Vaccine= genetically modified recombinant vaccine
  • Target is neonates born to HBV positive mum, healthcare workers, dialysis patients, young gay men and contacts of cases

Treatment options for HBV

  • Lamivudie- suppressions so decreases amount of virus so that it can’t cause disease
  • Interferon- switch off high grade infection- long term recovery
  • Transplant
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7
Q

What theronostic tests are available for HBV

A
  • Theronostic means to check if medication is working properly
    1. Lamivudine resistance- sequence the virus gene- usually will become resistant within 2 yrs
    2. HBV DNA- assess response to Lamivudine
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8
Q

Discuss the features of hepatitis C

A
  • Blood transmission= main route
  • Infects hepatocytes (direct viral effects and immune mediated inflammation)
  • 6 genotypes - type 1= poor prognosis and type 3 is good prognosis
  • Asymptomatic in acute stage
  • 70% develop acute infection
  • 20% develop cirrhosis
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9
Q

What are the various markers used in Hepatitis C

A
  • HCV antibody- past/ present infection
  • HCV RNA (by PCR)- Current infection
  • HCV genotype- guide for treatment type 1= 1-12 months and type 3= 6months

Current infection= Antibody + positive PCR
Past infection= Antibody positive and negative PCR

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10
Q

What are the treatment options for Hepatitis C

A
  • Interferon and ribavirin- treat high grade infection
  • Transplant- HCV recurs in 100% of grafts

Theronostic assays-

  • Genotype decides treatment duration
  • HCV RNA on PCR determines treatment response
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11
Q

Describe the features of HIV

A
  • Retrovirus -Common in subsaharan Africa
  • Infects immune cells CD4 lymphocytes (Th cells) and macrophages
  • Immunosuppression due to reduced T cell function
  • 2 main subtypes HIV 1 (most common) and HIV 2

2 diseases

  1. Primary HIV infection 10-25 days after exposure- glandular fever like illness , lymphadenopathy, rash, fever
  2. AIDS- 8 yr post exposure, opportunistic infections, weight loss
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12
Q

What are some of the opportunistic infections involved in AIDS

Viral
Bacterial
Protozoa
Fungi

A

Viral= CMV (retinitis), EBV (CNS, lymphoma) , JC polymavirus (encephalopathy)

Bacterial= Typical/ atypical mycobacteria- TB (major killer)

Protozoa= Toxoplasma (CNS infection), Cryptospoidia (bloody diarrhoea- life threatening)

Fungi= Candida (oesophageal) Pneumocytis (pneumonia), cryptococcus (meningitis)

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13
Q

How is HIV diagnosed and treated

A
  • HIV antibody = infection
  • 4 assays used to rule out any false positives

Treatment

  • Antiretroviral therapy- suppression
  • Combination therapy- 3 antiretroviral drugs from at least 2 classes

Classes of drugs

  • Nucleoside reverse transcriptase inhibitors
  • Non-nucleoside reverse transcriptase inhibitors
  • Protease inhibitors
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14
Q

How do you prevent mother to baby transmission of HIV

A
  1. C-section birth
  2. ART to mother and baby
  3. No breastfeeding
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15
Q

What theronostic assays are used in HIV

A
  • Viral load- viral RNA in blood
  • CD4 t lymphocyte count- determines response to treatment
  • Mutational analysis for drug resistance
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