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CD8(+)CXCR5(+) T Cells Regulate Pathology in the Genital Tract
We have identified a CD8(+)CXCR5(+) T cell that prevents the development of oviduct dilation following C. muridarum genital infection. Phenotypic studies show that CD8(+)CXCR5(+) cells express markers of T regulatory cells (FoxP3, CD25, and GITR) but do not express a necessary component of cytotoxic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556439/ https://www.ncbi.nlm.nih.gov/pubmed/23365491 http://dx.doi.org/10.1155/2013/813238 |
Sumario: | We have identified a CD8(+)CXCR5(+) T cell that prevents the development of oviduct dilation following C. muridarum genital infection. Phenotypic studies show that CD8(+)CXCR5(+) cells express markers of T regulatory cells (FoxP3, CD25, and GITR) but do not express a necessary component of cytotoxic cells (perforin). Cxcr5(−/−) mice have significantly lower numbers of CD8(+) cells and lack the CD8(+)CXCR5(+) population while the total number of CD4(+) cells is equivalent between mouse strains. The transfer of CD8(+) splenocytes from WT mice reduces the oviduct dilation seen in Cxcr5(−/−) mice following C. muridarum infection. Future studies will investigate the mechanism by which this cell type regulates genital tract pathology. |
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