Long-term evaluation of triple nucleoside therapy administered from primary HIV-1 infection

Objective: To study the long-term effect of triple-drug therapy initiated a t the time of primary HIV-1 infection and to evaluate the persistance of re plication-competent virus in responding patients. Methods: Prospective open-label pilot study. Patients received a combinatio n of zidovudine, didanosine and lamivudine. Viral sequencing of the reverse transcriptase gene was performed before therapy and during follow-up. HIV- 1 RNA and DNA as well as CD4 and CD8 T lymphocyte subsets were measured in blood and in lymph node biopsies during therapy. Isolated blood CD4 T cells were cultured in conditions that improved HIV isolation. Three patients re ceived in vivo interleukin-2 and gamma-interferon in older to try to identi fy intracellular pools of replication-competent virus. Setting: A tertiary care general hospital. Patients: Fifteen patients observed within 28 days following the acute retr oviral syndrome. Results: After a mean follow-up of 27.5 +/- 2.9 months, plasma RNA remained < 20 copies/ml (four patients), fluctuated between 20 and 120 copies/ml (s ix patients) or rebounded (five patients). M184V and/or T215Y mutations wer e demonstrated in two of these last five patients. Proviral DNA in peripher al blood mononuclear cells (PBMC) decreased by an average of similar to 1 l og after 16 +/- 3 months, reaching undetectable levels in three patients. T he culture of isolated CD4 T cells yielded virus in all but two patients. T hese last were characterized by a waning antibody reactivity on the Western blot, undetectable proviral DNA in PBMC and undetectable RNA in lymph node s. Cytokine administration in vivo had no effect in one patient and unmaske d plasma RNA in the other. Stopping therapy in the first patient led to a r ebound in plasma RNA. Conclusion: Despite a lack of detectable plasma viral activity in some pati ents after 3 years of triple nucleoside therapy administered since the acut e retroviral syndrome, replication-competent virus can still be demonstrate d. (C) 1999 Lippincott Williams & Wilkins.