| Literature DB >> 11023459 |
R T Schooley1, C Spino, D Kuritzkes, B D Walker, F A Valentine, M S Hirsch, E Cooney, G Friedland, S Kundu, T C Merigan, M J McElrath, A Collier, S Plaeger, R Mitsuyasu, J Kahn, P Haslett, P Uherova, V deGruttola, S Chiu, B Zhang, G Jones, D Bell, N Ketter, T Twadell, D Chernoff, M Rosandich.
Abstract
The potential role of human immunodeficiency virus type 1 (HIV-1)-specific immune responses in controlling viral replication in vivo has stimulated interest in enhancing virus-specific immunity by vaccinating infected individuals with HIV-1 or its components. These studies were undertaken to define patient populations most likely to respond to vaccination, with the induction of novel HIV-1-specific cellular immune responses, and to compare the safety and immunogenicity of several candidate recombinant HIV-1 envelope vaccines and adjuvants. New lymphoproliferative responses (LPRs) developed in <30% of vaccine recipients. LPRs were elicited primarily in study participants with a CD4 cell count >350 cells/mm(3) and were usually strain restricted. Responders tended to be more likely than nonresponders to have an undetectable level of HIV-1 RNA at baseline (P=.067). Induction of new cellular immune responses by HIV-1 envelope vaccines is a function of the immunologic stage of disease and baseline plasma HIV-1 RNA level and exhibits considerable vaccine strain specificity.Entities:
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Year: 2000 PMID: 11023459 DOI: 10.1086/315860
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226