Persistent alterations in T-cell repertoire, cytokine and chemokine receptor gene expression after 1 year of highly active antiretroviral therapy

Objectives: To examine T-cell repertoire modifications, the evolution of T- helper (TH)1/TH2 cytokine imbalance and modifications in chemokine receptor expression when the viral load is decreased by 2-3 log(10) copies/ml under highly active antiretroviral therapy (HAART). Design: Sixteen patients previously treated with zidovudine and lamivudine, with CD4 cells below 300 x 10(6)/l and viraemia above 30 000 copies/ml wer e treated by saquinavir and ritonavir together with both reverse transcript ase (RT) inhibitors (ANRS 069 trial). T-cell repertoire, chemokine receptor and lymphokine expression were studied from peripheral blood mononuclear c ells sampled at weeks 0, 24 and 48. Methods: T-cell repertoire study was carried out using the Immunoscope meth od. Interleukin (IL)-12 receptor beta 2, CC-chemokine receptor (CCR)-3, CXC -chemokine receptor-4 and CCR-5 expression in CD4+ cells was measured by ki netic quantitative PCR and IL-2, IL-4, IL-10, IL-13, interferon (IFN)-gamma were measured using a quantitative RT-PCR assay with homologous internal s tandards. Results: Repertoire alterations were more frequent in CD4- than in CD4+ cel ls and persisted despite undetectable viraemia. Increased CCR-3 expression and spontaneous IFN-gamma as well as mitogenic induced IL-13 were observed at baseline and decreased slightly under HAART. Conclusion: The CD8+ cell repertoire alterations were profound, whereas the CD4+ cell alterations were moderate and both persisted unchanged under HAA RT. The TH1/TH2 imbalance was more related to TH2 over-expression than to T H1 deficiency and persisted for at least 1 year under HAART. (C) 1999 Lippi ncott Williams & Wilkins.