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PMID: 1721107 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Human immunodeficiency virus genetic variation that can escape cytotoxic T cell recognition.

Nature ·Vol. 354 ·No. 6353 ·1991-12-12 ·Pages 453-9

Phillips RE, Rowland-Jones S, Nixon DF, Gotch FM, Edwards JP, Ogunlesi AO, Elvin JG, Rothbard JA, Bangham CR, Rizza CR

Abstract

In a longitudinal study of HIV seropositive patients, there were fluctuations in the specificity of cytotoxic T cells for the virus. This was matched by variability in proviral gag DNA epitope sequences in the lymphocytes of these patients. Some of these viral variants are not recognized by autologous T cells. Accumulation of such mutations in T-cell antigenic targets would provide a mechanism for immune escape.

MeSH Terms
Amino Acid Sequence Base Sequence Epitopes/genetics,immunology Genetic Variation/genetics,immunology HIV/genetics,immunology HIV Core Protein p24/genetics,immunology HIV Infections/complications,immunology,microbiology HIV Seropositivity/immunology Hemophilia A/complications Humans Longitudinal Studies Molecular Sequence Data Mutation/genetics,immunology Peptide Fragments/immunology T-Lymphocytes, Cytotoxic/immunology,microbiology
Chemicals
Epitopes HIV Core Protein p24 Peptide Fragments
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Phillips R E
Molecular Immunology Group, Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, UK.
Rowland-Jones S
Nixon D F
Gotch F M
Edwards J P
Ogunlesi A O
Elvin J G
Rothbard J A
Bangham C R
Rizza C R
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1991-12-12
Pages
453-9
Language
English
Region
England
NLM ID
0410462
Subset
IM
Grants
Wellcome Trust · United Kingdom
Corrections
CommentIn
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