Human immunodeficiency virus
From IDWiki
- A chronic immunodeficiency resulting from infection with the human immunodeficiency virus (HIV)
- Acquired immune deficiency syndrome (AIDS) is a severe form of HIV characterized by low CD4 count resulting in characteristic infections
Microbiology
- A member of the Retroviridae family
Clades / Subtypes
- HIV-1
- M group
- Clade A: common in East Africa
- Clade B: is common in Canada, Americas, Europe
- M group
- HIV-2
Life Cycle
- Two phases: initial viral attachment, fusion, reverse transcription, and integration; and the following lifetime of the viral infection
- Initial cellular infection
- Binding or attachment of the virion gp120 Env surface protein to the CD4 receptor with CCR5 or CXCR4 coreceptor (on macrophage or T-cell, respectively).
- Binding the receptor triggers a conformational change that exposes the fusion domain on gp41, which facilitates fusion and viral entry. The proceeding viral disassembly requires viral protein p24 to bind to cellular cyclophilin A.
- In the cytoplasm, reverse transcriptase converts viral RNA into viral DNA. The RNA is degraded, then the complementary strand of DNA created.
- The preintegration complex of double-stranded DNA is imported into the nucleus using viral Gag, viral protein R (Vpr), and integrase. Unlike other retroviruses, HIV does not require active replication to enter the nucleus.
- Infection of lymphoid cells and lymph nodes, especially gut-associated lymphoid tissue (GALT)
- Infection therefore kills a large proportion of CD4 cells in the gut
- HIV enters from the mucosa to infect activated Langerhans macrophages, which then get to the local lymphoid tissue
Epidemiology
- 63,000 Canadians living with HIV in 2016
- 14% don't know they have it
- Methods of acquisition in Canada
- MSM (52% of cases)
- People who inject drugs (17% of cases)
- Heterosexual sex (33% of cases)
Risk Factors
- High-risk exposures
- MSM
- Multiple partners
- Injection drug use
- Sex work
- Aboriginal Canadians (2.7x higher incidence)
- African and Caribbean people (endemic countries)
- Prior STIs
Presentation
Acute HIV/Seroconverion
- Incubation period 2 to 6 weeks
- Usually presents as an influenza-like illness
- Symptoms include fever, lymphadenopathy, rash, myalgias, arthralgias, headache, diarrhea, oral ulcers, leukopenia, thrombocytopenia, and mild hepatitis
Chronic HIV
- Fevers
- Weight loss
- Dyspnea, cough, hemoptysis
- Dysphagia, diarrhea
- Anemia, neutropenia, thrombocytopenia
- Metabolic derangements
- Opportunistic infections
Diagnosis
- HIV serology
- Can test for HIV antibodies (usually combined IgM/IgG) and p24 antigen
- Window period of 3-4 weeks exists before antibodies are positive, and is shortened to 2-3 weeks with antigen testing
- If concern for acute seroconversion syndrome (within 2-4 weeks of exposure), may need to repeat serology
- Standard testing in Ontario includes HIV 1+2 antigen/antibody ELISA screen, followed by confirmatory p24 antigen ELISA
- HIV qualitative PCR
- Indicated in cases of suspected acute seroconversion (with negative serology), previous indeterminate antibody results, or a newborn of an HIV-infected mother
- More specific than quantitative PCR for viral load
- Can be done from dried blood spot
- Generally only done for HIV-1 outside of a reference lab
Ab/Ag | Ab | Ag | RNA | Interpretation |
---|---|---|---|---|
– | HIV negative, or within serologic window period (2-3 weeks) | |||
– | + | HIV positive, within the serologic window period (2-3 weeks) | ||
+ | + | HIV positive, following a 3-4 week window period | ||
+ | – | + | HIV positive, within the serologic window period for antibodies (3-4 weeks) |
Investigations
- See Initial assessment for patients with HIV for baseline bloodwork
Management
Initial management
Follow-up
- See also Routine follow-up for patients with HIV
- HIV viral load
- Every 4 to 6 weeks until undetectable
- Then every 3 months until undetectable for 1 year
- Then every 6 months
- CD4 count
- Every 3 to 4 months until viral load undetectable and CD4 count >350 for 1 year
- Then every 6 months until viral load undetectable for at least 2 years and CD4 count > 500
- Then stop monitoring routinely unless evidence of treatment failure
- Assess for failure if RNA level remains detectable at 24 weeks or if it increases to above 50 at any time
- Repeat RNA level within 4 weeks