Two Double-Blinded, Randomized, Comparative Trials of 4 Human Immunodeficiency Virus Type 1 (HIV-1) Envelope Vaccines in HIV-1—Infected Individuals across a Spectrum of Disease Severity: AIDS Clinical Trials Groups 209 and 214

The potential role of human immunodeficiency virus type 1 (HIV-1)—specific immune responses in controlling viral replication in vivo has stimulatedinterest in enhancing virus-specificimmunity by vaccinating infected individuals with HIV-1 or its components. These studies were undertaken to define pa...

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Veröffentlicht in:The Journal of infectious diseases 2000-11, Vol.182 (5), p.1357-1364
Hauptverfasser: Schooley, Robert T., Spino, Cathie, Kuritzkes, Daniel, Walker, Bruce D., Valentine, Fred T., Hirsch, Martin S., Cooney, Elizabeth, Friedland, Gerald, Kundu, Smriti, Merigan, Thomas C., McElrath, M. Juliana, Collier, Ann, Plaeger, Susan, Mitsuyasu, Ronald, Kahn, James, Haslett, Patrick, Uherova, Patricia, deGruttola, Victor, Chiu, Simon, Zhang, Bin, Jones, Gayle, Bell, Dawn, Ketter, Nzeera, Twadell, Thomas, Chernoff, David, Rosandich, Mary
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Sprache:eng
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Zusammenfassung:The potential role of human immunodeficiency virus type 1 (HIV-1)—specific immune responses in controlling viral replication in vivo has stimulatedinterest in enhancing virus-specificimmunity 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 350 cells/mm3 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.
ISSN:0022-1899
1537-6613
DOI:10.1086/315860