Vδ1+ γδ T cells producing CC chemokines may bridge a gap between neutrophils and macrophages in innate immunity during Escherichia coli infection in mice

Yasunobu Yoshikai, Tetsuzo Tagawa, Kensuke Shibata, T. Yajima, H. Hara, K. Kishihara

Research output: Contribution to journalArticle

Abstract

An influx of neutrophils followed a short time later by an influx of macrophages to the infected site plays a key role in innate immunity against Escherichia coli infection. We found in this study that Vδ1-/- mice exhibited impaired accumulation of peritoneal macrophages but not neutrophils and delayed bacterial clearance after intraperitoneal inoculation with E. coli. Peritoneal γδ T cells from E. coli-infected wild-type mice produced CCL3/MIP-1α and CCL5/RANTES in response to γδ T CR triggering in vitro, while such production was not evident in γδ T cells from E. coli-infected Vδ1-/- mice. Neutralization of CCL3/MIP-1α by a specific monoclonal antibody in vivo significantly inhibited the accumulation of macrophages in the peritoneal cavity after E. coli infection, resulting in exacerbated bacterial growth in the peritoneal cavity. These results suggest that Vδ1+ γδ T cells bridge a gap between neutrophis and macrophages in innate immunity during E. coli infection mediated by production of CC chemokines, enhancing macrophage trafficking to the site of infection.

Original languageEnglish
Pages (from-to)155-159
Number of pages5
JournalInternational Congress Series
Volume1285
DOIs
Publication statusPublished - Nov 1 2005

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Escherichia coli Infections
CC Chemokines
Innate Immunity
Neutrophils
Macrophages
T-Lymphocytes
Peritoneal Cavity
Escherichia coli
Chemokine CCL5
Peritoneal Macrophages
Monoclonal Antibodies
Growth
Infection

All Science Journal Classification (ASJC) codes

  • Medicine(all)

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Vδ1+ γδ T cells producing CC chemokines may bridge a gap between neutrophils and macrophages in innate immunity during Escherichia coli infection in mice. / Yoshikai, Yasunobu; Tagawa, Tetsuzo; Shibata, Kensuke; Yajima, T.; Hara, H.; Kishihara, K.

In: International Congress Series, Vol. 1285, 01.11.2005, p. 155-159.

Research output: Contribution to journalArticle

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