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PMID: 6976410 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Antigen recognition by cloned cytotoxic T lymphocytes follows rules predicted by the altered-self hypothesis.

The Journal of experimental medicine ·Vol. 155 ·No. 1 ·1982-01-01 ·Pages 111-25

Hünig TR, Bevan MJ

Abstract

Radiation chimeras prepared by injecting H-2 heterozygous F1 stem cells into lethally irradiated parental hosts show a marked, but not absolute, preference for host-type H-2 antigens in the H-2-restricted cytotoxic T lymphocyte (CTL) response to minor histocompatibility (minor H) antigens. We have selected for the anti-minor HCTL that are restricted to the parental H-2 type absent from the chimeric host and found that in two out of eight cases, such CTL lysed target cells of either parental H-2 type. From one of these CTL populations that lysed H-2d and H-2k target cells expressing BALB minor H antigens, clones were derived and further analyzed. The results showed that: (a) lysis of both H-2d and H-2k target cells was H-2 restricted; (b) H-2d restriction mapped to Dd, and H-2k restriction mapped to Kk; (c) testing against various H-2d and H-2k strains of different and partially overlapping minor H backgrounds as well as against the appropriate F1 crosses revealed that in Dd- and Kk-restricted killing, different minor H antigens were recognized. In a second system, a CTL population was selected from normal (H-2d x H-2k)F1 mice that was specific for H-2d plus minor H antigens and for H-2k plus trinitrophenylated bovine serum albumin. We interpret these findings in terms of the altered-self hypothesis: The association of one H-2 antigen with one conventional antigen X may be recognized by the same T cell receptor specific for the complex formed by a different H-2 antigen in association with a second conventional antigen Y. The implications of these observations for the influence of self H-2 on the generation of the T cell receptor repertoire are discussed.

MeSH Terms
Animals Antigens Binding, Competitive Cattle Chromosome Mapping Clone Cells/immunology Cytotoxicity, Immunologic H-2 Antigens/genetics,immunology Haploidy Mice Mice, Inbred AKR Mice, Inbred C57BL Mice, Inbred DBA Radiation Chimera Serum Albumin, Bovine/immunology T-Lymphocytes/immunology Trinitrobenzenes/immunology
Chemicals
Antigens H-2 Antigens Trinitrobenzenes Serum Albumin, Bovine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hünig T R
Bevan M J
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23 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1982-01-01
Pages
111-25
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2186565
Subset
IM
Grants
NIAID NIH HHS · AI-14269 · United States
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