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PMID: 6970897 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Clones of helper T cells mediate antigen-specific, H-2-restricted DTH.

Nature ·Vol. 290 ·No. 5801 ·1981-03-05 ·Pages 62-3

Bianchi AT, Hooijkaas H, Benner R, Tees R, Nordin AA, Schreier MH

Abstract

It is now well established that in the mouse, helper T cells and killer T cells are two distinct thymus-derived lymphocyte subpopulations, differing from each other in Lyt phenotype and H-2 restriction, among other parameters. Helper T cells are Lyt-1+ and their action in immune responses involves restriction at the H-2I region of the major histocompatibility complex (MHC). Killer cells, on the other hand, are Lyt-23+ and their activity is restricted by H-2K/D (refs 1, 3). In most instances, T cells mediating delayed-type hypersensitivity (DTH) responses share the Lyt phenotype and H-2 restriction of the helper T cell. This raises the question of whether or not helper activity and DTH can be mediated by the same activated T cell. Arguments for both views have been reported. We analysed this question using clones of specific helper T cells, which were obtained by long-term culture in vitro of in vivo primed T cells, followed by single-cell cloning. Here we show that these clones of helper T cells mediate antigen-specific and fully H-2-restricted DTH. The restricting element lies to the left of the I-B region in genetic maps of the mouse MHC.

MeSH Terms
Animals Cells, Cultured Clone Cells/immunology H-2 Antigens/immunology Horses/immunology Hypersensitivity, Delayed/immunology Mice Mice, Inbred Strains/immunology Sheep/immunology T-Lymphocytes/immunology,physiology,transplantation Transplantation, Heterologous Transplantation, Homologous
Chemicals
H-2 Antigens
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Bianchi A T
Hooijkaas H
Benner R
Tees R
Nordin A A
Schreier M H
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1981-03-05
Pages
62-3
Language
English
Region
England
NLM ID
0410462
Subset
IM
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