There is, at present, no cure for HIV infection.
The core component of treatment and care of patients living with HIV is provision of antiretroviral therapy (ART) (1). Seek specialist advice regarding antiviral therapy.
ART can be divided into six classes based on their molecular mechanisms and resistance profiles:
In addition, two drugs, ritonavir (an old HIV drug given at subtherapeutic doses) and cobicistat are used as pharmacokinetic enhancers (or boosters) to enhance the blood levels (2).
Mutation of the HIV during replication has led to rapid development of resistance to most single anti-HIV drugs. Due to this reason anti-HIV drugs are used in combinations of three or more.
The decision to initiate ART should be based on two different CD4 counts, ideally at least 7 days apart because of variability in the CD4 count itself and to rule out laboratory mistakes and other variances (for example, concurrent illnesses).
WHO recommendations for initiating ART for patients with HIV:
| CD4 cell count | recommendation |
1 | <200/mm3 | treat |
200-350/mm3 | consider treatment | |
2 | <200/mm3 | treat |
200-350/mm3 | consider treatment | |
3 | 200-350/mm3 | treat |
4 | regardless of CD4 count | treat |
All patients should be regularly monitored for treatment success of ART:
| virological | immunological | clinical | |
marker | viral load | CD4 cell count | clinical stage | |
time | 24 weeks | 48 weeks | 24-48 weeks | by 12 weeks of treatment initiation should be asymptomatic or have few symptoms |
suggested ranges | <400 copies/ml | <50 copies/ml | increase from baseline by at least 50-100 cells/mm3 | stage 1 or 2 |
During early weeks of treatment, the speed of the viral load reduction should be monitored and if the speed of reduction is insufficient treatment failure due to adherence problems, inadequate drug levels or pre-existing primary drug resistance should be taken in to account (5).
Drug resistance to ART may arise due to: non-adherence to medication or drug-drug interactions and, once established, is irreversible. Cross-resistance between classes of drugs means treatment choices are further limited.
There is little data available on which to base the decision on whether to start treatment in primary (acute) HIV infection. UK guidelines recommend that all individuals with suspected or diagnosed PHI are reviewed promptly by an HIV specialist and offered immediate ART (4)
During the later stages of HIV infection management is based heavily the treatment of HIV-related infections or illnesses as they occur. On occasion, tissue biopsy may be necessary and this may often throws up surprises, reflecting the multiple pathology of the condition.
CD4 cell count-guided antiretroviral treatment interruption strategy
Reference:
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