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PMID: 1946358 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Priming of anti-human immunodeficiency virus (HIV) CD8+ cytotoxic T cells in vivo by carrier-free HIV synthetic peptides.

Hart MK, Weinhold KJ, Scearce RM, Washburn EM, Clark CA, Palker TJ, Haynes BF

Abstract

The generation of antiviral cytotoxic T lymphocytes (CTLs) is a critical component of the immune response to viral infections. A safe and nontoxic vaccine for AIDS would optimally use a carrier-free synthetic peptide immunogen containing only components of HIV necessary for induction of protective immune responses. We report that hybrid synthetic peptides containing either a HIV envelope gp120 T-cell determinant (T1) or the envelope gp41 fusion domain (F) N-terminal to HIV CTL determinants are capable of priming murine CD8+, major histocompatibility complex class I-restricted anti-HIV CTLs in vivo. These data demonstrate that carrier-free, nonderivatized synthetic peptides can be used in vivo to induce anti-HIV CTL responses.

MeSH Terms
Amino Acid Sequence Animals CD8 Antigens/analysis H-2 Antigens/immunology HIV Antigens/chemistry HIV Envelope Protein gp120/chemistry,immunology HIV-1/immunology Immunologic Memory Major Histocompatibility Complex Mice Mice, Inbred BALB C Mice, Inbred C57BL Molecular Sequence Data Peptides/immunology T-Lymphocytes, Cytotoxic/immunology
Chemicals
CD8 Antigens H-2 Antigens HIV Antigens HIV Envelope Protein gp120 Peptides
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Hart M K
Department of Medicine, Duke University Medical Center, Durham, NC 27710.
Weinhold K J
Scearce R M
Washburn E M
Clark C A
Palker T J
Haynes B F
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1991-11-01
Pages
9448-52
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC52735
Subset
IM
Grants
PHS HHS · A128662 · United States
NCI NIH HHS · CA28936 · United States
NCI NIH HHS · CA43447 · United States
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