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PMID: 2957443 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Complexity of T cell receptor recognition sites for defined alloantigens.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 139 ·No. 6 ·1987-09-15 ·Pages 1952-9

Borst J, de Vries E, Spits H, de Vries JE, Boylston AW, Matthews EA

Abstract

Three monoclonal antibodies react with the T cell receptor on the tumor line HPB-ALL and in addition with 3 to 13% of human peripheral blood T cells of normal donors. These antibodies are shown to react with an epitope encoded by the V beta 5 family of T cell receptor beta-chain variable region gene segments. Cells expressing V beta 5 gene segments can have cytotoxic or helper function, be of the T4+ or T8+ phenotype, and have specificity for either class I or class II major histocompatibility complex alloantigens. Seven T cell clones were generated, which express V beta 5 and are specific for the HLA-A2 molecule. With the use of these clones, we illustrate how isoelectric focusing can be used to analyze T cell receptor alpha- and beta-chain structure. The seven clones recognize five distinct conformational determinants on HLA-A2. They procure different binding sites by the use of different alpha-chains, J beta sequences, or both.

MeSH Terms
Amino Acid Sequence Binding Sites Cell Line Cytotoxicity, Immunologic HLA Antigens/immunology Humans Isoelectric Point Peptide Fragments/physiology Receptors, Antigen, T-Cell/physiology Receptors, Antigen, T-Cell, alpha-beta T-Lymphocytes, Cytotoxic/immunology
Chemicals
HLA Antigens Peptide Fragments Receptors, Antigen, T-Cell Receptors, Antigen, T-Cell, alpha-beta
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Borst J
de Vries E
Spits H
de Vries J E
Boylston A W
Matthews E A
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1987-09-15
Pages
1952-9
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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