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CD8α-Deficient Mice Are Highly Susceptible to 5-Fluorouracil-Induced Lethality
Author(s) -
Naoto Itoh,
Hitoshi Nishimura,
Tetsuya Matsuguchi,
Toshiki Yajima,
Yasuji Mokuno,
Takashi Hiromatsu,
Yuji Nimura,
Yasunobu Yoshikai
Publication year - 2002
Publication title -
clinical and vaccine immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.649
H-Index - 77
eISSN - 1556-6811
pISSN - 1556-679X
DOI - 10.1128/cdli.9.3.550-557.2002
Subject(s) - cd8 , intraepithelial lymphocyte , biology , intestinal mucosa , microbiology and biotechnology , alpha (finance) , immunology , antigen , medicine , immune system , construct validity , nursing , patient satisfaction
Intestinal intraepithelial lymphocytes (i-IEL) expressing CD8 alpha are located in the intestine and may confer protection against invasion of intestinal microflora. We found that mice rendered deficient in CD8 alpha molecules by homologous recombination were susceptible to 5-fluorouracil (5-FU)-induced lethality accompanied by translocation of members of the enterobacteria. The number of i-IEL was greatly reduced on day 6 after 5-FU administration in both CD8 alpha(+/-) mice and CD8 alpha(-/-) mice, whereas the recovery of the level of i-IEL thereafter was significantly impaired in CD8 alpha(-/-) mice compared with that in CD8 alpha(+/-) mice. The ability of i-IEL to produce gamma interferon in response to immobilized T-cell receptor (TCR) alpha beta or TCR gamma delta monoclonal antibodies was significantly lower in CD8 alpha(-/-) mice than in CD8 alpha(+/-) mice. Transfer of CD8(+) i-IEL conferred significant protection against 5-FU-induced lethality in CD8 alpha(-/-) mice. The results suggest that CD8(+) i-IEL play an important role in protection against 5-FU-induced lethality with translocation of Enterobacteriaceae.

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