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PMID: 1826020 Published · ppublish English Journal Article

Detection of cytotoxic T lymphocytes specific for synthetic peptides of gp160 in HIV-seropositive individuals.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 146 ·No. 7 ·1991-04-01 ·Pages 2214-9

Clerici M, Lucey DR, Zajac RA, Boswell RN, Gebel HM, Takahashi H, Berzofsky JA, Shearer GM

Abstract

Four synthetic peptides corresponding to the IIIB sequence of gp160 of HIV were recently reported to stimulate Th cell function by PBL from HIV-infected, asymptomatic patients. In the present report, we used these same peptides to demonstrate CTL activity in a similar patient population. EBV-transformed B-cell lines from asymptomatic, HIV seropositive and seronegative control donors were pre-incubated with the peptides. Fresh PBL from 19 (76%) of 25 HIV seropositive donors lysed autologous targets pulsed with at least one of the four peptides. Autologous targets pulsed with two non-immunogenic peptides were not lysed. PBL from none of the eight HIV seronegative controls lysed peptide-preincubated autologous targets. The CTL activity was mediated by T cells, was predominantly MHC class I restricted, and was increased by in vitro restimulation of PBL with the peptides. HLA A-2 was identified as a restricting element for all four peptides in different patients, and for three of the peptides in the same donor. HLA-A1 or -B8 may also present some of the peptides. Thus, the same peptides can be recognized by human Th cells and class I MHC-restricted CTL.

MeSH Terms
Cytotoxicity, Immunologic Gene Products, env/immunology HIV Envelope Protein gp120/immunology HIV Envelope Protein gp160 HIV Seropositivity/immunology Histocompatibility Antigens Class I/immunology Humans Immunity, Cellular Peptides/immunology Protein Precursors/immunology T-Lymphocytes, Cytotoxic/immunology T-Lymphocytes, Helper-Inducer/immunology
Chemicals
Gene Products, env HIV Envelope Protein gp120 HIV Envelope Protein gp160 Histocompatibility Antigens Class I Peptides Protein Precursors
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Clerici M
Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Lucey D R
Zajac R A
Boswell R N
Gebel H M
Takahashi H
Berzofsky J A
Shearer G M
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1991-04-01
Pages
2214-9
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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