BMC Infectious Diseases (Feb 2008)

Immunological predictors of CD4<sup>+ </sup>T cell decline in antiretroviral treatment interruptions

  • Gonzalez-García Juan,
  • Rubio Rafael,
  • Moreno Ana,
  • de Quiros Juan,
  • Moreno Santiago,
  • Resino Salvador,
  • Seoane Elena,
  • Arribas José,
  • Pulido Federico,
  • Muñoz-Fernández Ma Ángeles

DOI
https://doi.org/10.1186/1471-2334-8-20
Journal volume & issue
Vol. 8, no. 1
p. 20

Abstract

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Abstract Background The common response to stopping anti-HIV treatment is an increase of HIV-RNA load and decrease in CD4+, but not all the patients have similar responses to this therapeutic strategy. The aim was to identify predictive markers of CD4+ cell count declines to Methods 27 HIV-infected patients participated in a prospective multicenter study in with a 24 month follow-up. Patients on stable highly active antiretroviral therapy (HAART), with CD4+ count > 600/μL, and HIV-RNA + cell count to Results After 24 months of follow-up, 16 of 27 (59%) patients (who discontinued therapy) experienced declines in CD4+ cell count to + nadir of Mycobacterium tuberculosis purified protein derivative (PPD) below 10000 c.p.m. at baseline (4.77 (1.07; 21.12)), IL-4 production above 100 pg/mL at baseline (5.95 (1.76; 20.07)) in PBMC cultured with PPD, and increased IL-4 production of PBMC with p24 antigen at baseline (1.25 (1.01; 1.55)) were associated to declines in CD4+ cell count to Conclusion Both the number (CD4+ nadir) and the functional activity of CD4+ (lymphoproliferative response to PPD) predict the CD4+ decrease associated with discontinuation of ART in patients with controlled viremia.