KATOU Hidehito
Department School of Medicine, School of Medicine Position |
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Article types | Original article |
Language | English |
Peer review | Peer reviewed |
Title | High affinity of interaction between superantigen and TCR Vβ molecules induces a high level and prolonged expansion of superantigen-reactive CD4+ T cells. |
Journal | Formal name:The Journal of biological chemistry Abbreviation:J Biol Chem ISSN code:00219258/1083351X |
Volume, Issue, Page | 285(40),pp.30427-30435 |
Author and coauthor | OMOE Katsuhiko† ,NUNOMURA Wataru ,KATO Hidehito ,LI Zhong-Juan ,IGARASHI Osamu ,ARAAKE Minako ,SANO Keigo ,ONO Hisaya K ,ABE Yohei ,HU Dong-Liang ,NAKANE Akio ,KIYONO Hiroshi ,TAKAKUWA Yuichi ,SHINAGAWA Kunihiro ,UCHIYAMA Takehiko ,IMANISHI Ken'ichi* |
Publication date | 2010/10 |
Summary | In mice implanted with an osmotic pump filled with the superantigen (SAG) staphylococcal enterotoxin A (SEA), the Vbeta3+CD4+ T cells exhibited a high level of expansion whereas the Vbeta11+CD4+ T cells exhibited a mild level of expansion. In contrast, in mice implanted with an osmotic pump filled with SE-like type P (SElP, 78.1% homologous with SEA), the Vbeta11+CD4+ T cells exhibited a high level of expansion while the Vbeta3+CD4+ T cells exhibited a low level of expansion, suggesting that the level of the SAG-induced response is determined by the affinities between the TCR Vbeta molecules and SAG. Analyses using several hybrids of SEA and SElP showed that residue 206 of SEA determines the response levels of Vbeta3+CD4+ and Vbeta11+CD4+ T cells both in vitro and in vivo. Analyses using the above-mentioned hybrids showed that the binding affinities between SEA and the Vbeta3/Vbeta11 beta chains and between SEA-MHC class II-molecule complex and Vbeta3+/Vbeta11+ CD4+ T cells determines the response levels of the SAG-reactive T cells both in vitro and in vivo. |