Poor CD4 T cell restoration after suppression of HIV-1 replication may reflect lower thymic function

Objective: To characterize immune phenotype and thymic function in HIV-1-in fected adults with excellent virologic and poor immunologic responses to hi ghly active antiretroviral therapy (HAART). Methods: Cross-sectional study of patients with CD4 T cell rises of greater than or equal to 200 x 10(6) cells/I (CD4 responders; n = 10) or < 100 x 1 0(6) cells/I (poor responders; n = 12) in the first year of therapy. Results: Poor responders were older than CD4 responders (46 versus 38 years ; P < 0.01) and, before HAART, had higher CD4 cell counts (170 versus 35 x 10(6) cells/l; P = 0.11) and CD8 cell counts (780 versus 536 x 10(6) cells/ I; P = 0.02). After a median of 160 weeks of therapy, CD4 responders had mo re circulating naive phenotype (CD45+CD62L+) CD4 cells (227 versus 44 x 10( 6) cells/I; P = 0.001) and naive phenotype CD8 cells (487 versus 174 x 10(6 ) cells/I; P = 0.004) than did poor responders (after 130 weeks). Computed tomographic scans showed minimal thymic tissue in 11/12 poor responders and abundant tissue in 7/10 responders (P = 0.006). Poor responders had fewer CD4 cells containing T cell receptor excision circles (TREC) compared with CD4 responders (2.12 versus 27.5 x 10(6) cells/I; P = 0.004) and had shorte r telomeres in CD4 cells (3.8 versus 5.3 kb; P = 0.05). Metabolic labeling studies with deuterated glucose indicated that the lower frequency of TREC- containing lymphocytes in poor responders was not caused by accelerated pro liferation kinetics. Conclusion: Poor CD4 T cell increases observed in some patients with good v irologic response to HAART may be caused by failure of thymic T cell produc tion. (C) 2001 Lippincott Williams & Wilkins.