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PMID: 7481824 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cytotoxic T lymphocyte lysis inhibited by viable HIV mutants.

Science (New York, N.Y.) ·Vol. 270 ·No. 5240 ·1995-11-24 ·Pages 1360-2

Meier UC, Klenerman P, Griffin P, James W, Köppe B, Larder B, McMichael A, Phillips R

Abstract

Immune evasion by the human immunodeficiency virus (HIV) is unexplained but may involve the mutation of viral antigens. When cytotoxic T lymphocytes engaged CD4-positive cells that were acutely infected with HIV bearing natural variant epitopes in reverse transcriptase, substantial inhibition of specific antiviral lysis was observed. Mutant viruses capable of these transactive effects could facilitate the persistence of a broad range of HIV variants in the face of an active and specific immune response.

MeSH Terms
Amino Acid Sequence Antigenic Variation Base Sequence CD4-Positive T-Lymphocytes/immunology,virology Cell Line Cytotoxicity, Immunologic Epitopes/genetics HIV Antigens/genetics,immunology HIV Reverse Transcriptase HIV-1/enzymology,genetics,immunology HLA-B8 Antigen/immunology Humans Immune Tolerance Molecular Sequence Data RNA-Directed DNA Polymerase/genetics,immunology Receptors, Antigen, T-Cell/immunology T-Lymphocytes, Cytotoxic/immunology
Chemicals
Epitopes HIV Antigens HLA-B8 Antigen Receptors, Antigen, T-Cell HIV Reverse Transcriptase RNA-Directed DNA Polymerase
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Meier U C
Nuffield Department of Clinical Medicine, John Radcliffe Hospital, Headington, Oxford, UK.
Klenerman P
Griffin P
James W
Köppe B
Larder B
McMichael A
Phillips R
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1995-11-24
Pages
1360-2
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
Wellcome Trust · United Kingdom
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