HUMAN-IMMUNODEFICIENCY-VIRUS REVERSE-TRANSCRIPTASE T-HELPER EPITOPES IDENTIFIED IN MICE AND HUMANS - CORRELATION WITH A CYTOTOXIC T-CELL EPITOPE

被引:34
作者
DEGROOT, AS
CLERICI, M
HOSMALIN, A
HUGHES, SH
BARND, D
HENDRIX, CW
HOUGHTEN, R
SHEARER, GM
BERZOFSKY, JA
机构
[1] NCI, METAB BRANCH, MOLEC IMMUNOGENET & VACCINE RES SECT, BETHESDA, MD 20892 USA
[2] NCI, EXPTL IMMUNOL BRANCH, BETHESDA, MD 20892 USA
[3] NCI, FREDERICK CANC RES FACIL, ABL BASIC RES PROGRAM, FREDERICK, MD 21701 USA
[4] DEV CTR, FREDERICK, MD USA
[5] USAF, MED CTR, HIV UNIT, LACKLAND AFB, TX 78236 USA
[6] TORREY PINES INST MOLEC STUDIES, SAN DIEGO, CA USA
关键词
D O I
10.1093/infdis/164.6.1058
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell immunity may be critical to development of a vaccine for human immunodeficiency virus (HIV-1). T helper epitopes were identified in three predominantly conserved regions in the HIV-1 reverse transcriptase by using reverse transcriptase-immunized mice of five major histocompatibility complex haplotypes. One peptide (residues 38-52) that stimulated H-2k T cells also contained an epitope recognized by cytotoxic T cells from the same mice and from HIV-infected patients. Such concordance between helper and cytotoxic T lymphocyte epitopes, observed in four cases, may be important in vaccine development. Peptide 36-52 was recognized by interleukin-2-producing peripheral blood T cells from 9 of 17 HIV-seropositive humans studied, of multiple human leukocyte antigen-DR and -DQ types. The broad recognition of this peptide by both helper and cytotoxic T cells substantiates its potential importance in a vaccine.
引用
收藏
页码:1058 / 1065
页数:8
相关论文
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