TY - JOUR
T1 - Human CD4+ Cytolytic T Lymphocyte Responses to a Human Immunodeficiency Virus Type 1 gp160 Subunit Vaccine
AU - Siliciano, Robert F.
AU - Stanhope, Patricia E.
AU - Clements, Mary Lou
N1 - Funding Information:
Received 13 October 1992; revised 8 March 1993. Informed consent was obtained from all participants. National Institutes of Health and institutional guidelines for the conduct ofclinical research were followed. Financial support: National Institutes of Health (AI-28I 08, AI-322871. AI-05061 ). Reprints or correspondence: Dr. Robert Siliciano, Dept. of Medicine. Johns Hopkins University School of Medicine. 1049 Ross Bldg., 720 Rutland Ave., Baltimore, MD 21205.
PY - 1993/7
Y1 - 1993/7
N2 - The development of an effective vaccine against human immunodeficiency virus type 1 (HIV- 1) may require immunization protocols that elicit cytolytic T lymphocytes (CTL) in addition to neutralizing antibodies. This report demonstrates that vaccination of 4 HIV-L-seronegative volunteers with a recombinant HIV-1 gpI60 vaccine produced in mammalian cells elicited a CTL response in 3. The observed CTL activity was not mediated by classic CD8+ CTL but rather by cells of the CD4+ phenotype. The level of CTL activity varied over time, did not correlate with the proliferative response to gpI60, and was not increased by repeated immunization. At the clonal level, the vaccine was shown to elicit a functionally heterogeneous CD4+ T cell response that included clones with antigen-specific, major histocompatibility complex-restricted cytolytic activity. These clones were capable oflysing target cells expressing the HIV-1 env gene and thus might be active against HIV-1-infected cells in vivo.
AB - The development of an effective vaccine against human immunodeficiency virus type 1 (HIV- 1) may require immunization protocols that elicit cytolytic T lymphocytes (CTL) in addition to neutralizing antibodies. This report demonstrates that vaccination of 4 HIV-L-seronegative volunteers with a recombinant HIV-1 gpI60 vaccine produced in mammalian cells elicited a CTL response in 3. The observed CTL activity was not mediated by classic CD8+ CTL but rather by cells of the CD4+ phenotype. The level of CTL activity varied over time, did not correlate with the proliferative response to gpI60, and was not increased by repeated immunization. At the clonal level, the vaccine was shown to elicit a functionally heterogeneous CD4+ T cell response that included clones with antigen-specific, major histocompatibility complex-restricted cytolytic activity. These clones were capable oflysing target cells expressing the HIV-1 env gene and thus might be active against HIV-1-infected cells in vivo.
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U2 - 10.1093/infdis/168.1.92
DO - 10.1093/infdis/168.1.92
M3 - Article
C2 - 8099941
AN - SCOPUS:0027175821
SN - 0022-1899
VL - 168
SP - 92
EP - 100
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 1
ER -