Volume 19, Issue 10 pp. 1861-1865
Article
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Allo-class i-reactive cd4-cd8- t cell hybridomas recognize the conformational change of class i molecule resulting from the exchange of the α3 domain

Junji Yamamoto

Junji Yamamoto

Department of Immunology, Institute of Medical Science, University of Tokyo, Tokyo

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Manabu Tanabe

Manabu Tanabe

Department of Immunology, Institute of Medical Science, University of Tokyo, Tokyo

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Mutsuhiko Minami

Mutsuhiko Minami

Department of Blood Transfusion, School of Medicine, University of Tokyo, Tokyo

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Kyoichi Kano

Kyoichi Kano

Department of Immunology, Institute of Medical Science, University of Tokyo, Tokyo

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Masafumi Takiguchi

Corresponding Author

Masafumi Takiguchi

Department of Immunology, Institute of Medical Science, University of Tokyo, Tokyo

Department of Immunology, Institute of Medical Science, University of Tokyo, 4-6-1, Shirokanedai, Minato-ku, Tokyo 108, JapanSearch for more papers by this author
First published: October 1989
Citations: 1

Abstract

H-2Kb-reactive, interleukin (IL) 2-producing T cell hybridomas possessing neither CD8 nor CD4 molecules were employed for the study of allorecognition on interspecies hybrid antigens by T cells in the absence of an influence of these accessory molecules. Both HTB176.10 and HTB177.2 T cell hybridomas reacted with KbKbB7 hybrid antigens as well as Kb antigens and they produced more IL2 in response to Kb antigens than KbKbB7 hybrid antigens. IL2 production of these T cell hybridomas was dependent on the surface expression level of Kb molecules on stimulators. Therefore, L cells expressing almost equivalent levels of Kb or hybrid antigens were selected for further functional studies by these T cell hybridomas. They apparently produced less IL2 in response not only to interspecies hybrid antigens but also to interspecies hybrid antigens in response to Kb antigens. These results indicated that T cell hybridomas recognized the conformational change of class I molecule resulting from the exchange of the α3 domain via their T cell receptors.

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