FN: HIV Flashcards
Immunology
- HIV binds via gp 120 to CD4 - Th cells, monocytes, macrophages, neural cells
- CD4+ cells migrate to lymphoid tissue where virus replicates –> infectino of new CD4+ cells
- Depletion and impaired function of CD4+ cells - immune dysfunction
Virology
- RNA retrovirus
- After entry, viral reverse transcriptase makes DNA copy of viral RNA genome
- Viral integrase enzyme integrates this with host DNA
- Core viral proteins synthesised by host and then cleaved by viral protease into mature subunits
- Completeed virions released by budding
Natural Hx
- Acute infection: usually asympto
- Seroconversion
- Asymptomatic infection
Seroconversion
- Transient illness 2-6 wks after exposure
- Fever, malaise, myalgia, pharyngitis, macpap rash
- Rarely meningoencephalitis
Asymptomatic infections
But 30% will have PGL
- Notes >1 cm in diameter
- > 2 extra-inguinal sites
- > 3mo
AIDS related Complex
- AIDS prodrome
- Constitutional symptoms: fever, night sweats, wt. loss
- Minor opportunistic infections
- Oral candida - Oral hairy leukoplakia (EBV)
- Recurrent HSV
- Seborrhoeic dermatitis
AIDS
Defining illness
CD4 usually
OTher effects of HIV
- OSteoporosis
- Dementia
- Neuropathy
- Nephropathy
Diagnosis
- ELISA: detect serum (or salivary) anti-HIV abs
- Western Blot: for confirmation
- PCR: can detect HIV virions in the windown period
- Rapid antibody tests: false positives are a problem and results should be confirmed by western blot
Recent exposure window for diagnosis
Usually 1-3 wks
Can be 3-6 months
Investigations
- HIV diagnostic tests
- Drug resistance studies e.g. genotyping for reverse transcriptase or protease mutations
- Mantoux test
- Serology: toxo, CMV, HBV, HCV, syphilis
Monitoring
CD4 count
Viral load (HIV RNA)
FBC, U+E, LFTs, lipids, glucose
HAART indications
CD4
REgimens
1 NNRTI + 2 NRTIs
PI+ 2 NRTIs
1 NNRTI + 2 NRTIs
NNRTI - efavirenz
NRTI - emtricitabine + tenofovir (Truvada)
Atripla - efavirenz + emtricitabine + tenofovir
PI + 2 NRTIs
PI = lopinavir (+ low dose ritonavir = kaletra)
Aim of Regimens
- Undetectable VL after 4mo
- If VL remains high despite good compliance
- Change to a new drug combination
- Request resistance studies
Prophylaxis
CD4
HIV exposure
- Seroconversion post-needle-stick = 0.3% (1/300)
- Report to occupational health
- Immunise agaisnt hep B (active + passive)
- TEst blood form both parties: HIV, HBC, HCV
- Repeat recipient testing @ 3 and 6mo
Pep start and used for
Start PEP in high-risk exposure form HIV+ or unknown source
Start ASAP as possible
Continue for at least 28d
E.g. Truvade + Kaletra