Your browser doesn't support javascript.
loading
Delineation of the innate and adaptive T-cell immune outcome in the human host in response to Campylobacter jejuni infection.
Edwards, Lindsey A; Nistala, Kiran; Mills, Dominic C; Stephenson, Holly N; Zilbauer, Matthias; Wren, Brendan W; Dorrell, Nick; Lindley, Keith J; Wedderburn, Lucy R; Bajaj-Elliott, Mona.
Afiliación
  • Edwards LA; Infectious Diseases and Microbiology, Institute of Child Health, London, United Kingdom.
PLoS One ; 5(11): e15398, 2010 Nov 09.
Article en En | MEDLINE | ID: mdl-21085698
BACKGROUND: Campylobacter jejuni is the most prevalent cause of bacterial gastroenteritis worldwide. Despite the significant health burden this infection presents, molecular understanding of C. jejuni-mediated disease pathogenesis remains poorly defined. Here, we report the characterisation of the early, innate immune response to C. jejuni using an ex-vivo human gut model of infection. Secondly, impact of bacterial-driven dendritic cell activation on T-cell mediated immunity was also sought. METHODOLOGY: Healthy, control paediatric terminal ileum or colonic biopsy tissue was infected with C. jejuni for 8-12 hours. Bacterial colonisation was followed by confocal microscopy and mucosal innate immune responses measured by ELISA. Marked induction of IFNγ with modest increase in IL-22 and IL-17A was noted. Increased mucosal IL-12, IL-23, IL-1ß and IL-6 were indicative of a cytokine milieu that may modulate subsequent T-cell mediated immunity. C. jejuni-driven human monocyte-derived dendritic cell activation was followed by analyses of T cell immune responses utilising flow cytometry and ELISA. Significant increase in Th-17, Th-1 and Th-17/Th-1 double-positive cells and corresponding cytokines was observed. The ability of IFNγ, IL-22 and IL-17 cytokines to exert host defence via modulation of C. jejuni adhesion and invasion to intestinal epithelia was measured by standard gentamicin protection assay. CONCLUSIONS: Both innate and adaptive T cell-immunity to C. jejuni infection led to the release of IFNγ, IL-22 and IL-17A; suggesting a critical role for this cytokine triad in establishing host anti-microbial immunity during the acute and effectors phase of infection. In addition, to their known anti-microbial functions; IL-17A and IL-17F reduced the number of intracellular C. jejuni in intestinal epithelia, highlighting a novel aspect of how IL-17 family members may contribute to protective immunity against C. jejuni.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfocitos T / Campylobacter jejuni / Citocinas / Intestino Delgado Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2010 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfocitos T / Campylobacter jejuni / Citocinas / Intestino Delgado Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2010 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos