Infected site-restricted Foxp3+ natural regulatory T cells are specific for microbial antigens

被引:249
作者
Suffia, IJ
Reckling, SK
Piccirillo, CA
Goldszmid, RS
Belkaid, Y [1 ]
机构
[1] NIAID, Mucosal Immunol Unit, NIH, Bethesda, MD 20892 USA
[2] NIAID, Immunobiol Sect, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[3] Cincinnati Childrens Hosp Res Fdn, Div Mol Immunol, Cincinnati, OH 45229 USA
[4] McGill Univ, Dept Microbiol, Montreal, PQ H3A 2BA, Canada
[5] McGill Univ, Dept Immunol, Montreal, PQ H3A 2BA, Canada
[6] McGill Univ, Ctr Study Host Resistance, Montreal, PQ H3A 2BA, Canada
关键词
D O I
10.1084/jem.20052056
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural regulatory T (T reg) cells are involved in control of the immune response, including response to pathogens. Previous work has demonstrated that the repertoire of natural T reg cells may be biased toward self-antigen recognition. Whether they also recognize foreign antigens and how this recognition contributes to their function remain unknown. Our studies addressed the antigenic specificity of natural T reg cells that accumulate at sites of chronic infection with Leishmania major in mice. Our results support the idea that natural T reg cells are able to respond specifically to foreign antigens in that they strongly proliferate in response to Leishmania-infected dendritic cells, they maintain Foxp3 expression, and Leishmania-specific T reg cell lines can be generated from infected mice. Surprisingly, the majority of natural T reg cells at the infected site are Leishmania specific. Further, we showed that parasite-specific natural T reg cells are restricted to sites of infection and that their survival is strictly dependent on parasite persistence.
引用
收藏
页码:777 / 788
页数:12
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