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.
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20 March 2006
Article|
March 13 2006
Infected site-restricted Foxp3+ natural regulatory T cells are specific for microbial antigens
Isabelle J. Suffia,
Isabelle J. Suffia
1Mucosal Immunology Unit
3Division of Molecular Immunology, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229
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Stacie K. Reckling,
Stacie K. Reckling
3Division of Molecular Immunology, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229
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Ciriaco A. Piccirillo,
Ciriaco A. Piccirillo
4Department of Microbiology, Department of Immunology, and Center for the Study of Host Resistance, McGill University, Montreal, Quebec H3A 2BA, Canada
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Romina S. Goldszmid,
Romina S. Goldszmid
2Immunobiology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD 20892
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Yasmine Belkaid
Yasmine Belkaid
1Mucosal Immunology Unit
3Division of Molecular Immunology, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229
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Isabelle J. Suffia
1Mucosal Immunology Unit
3Division of Molecular Immunology, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229
Stacie K. Reckling
3Division of Molecular Immunology, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229
Ciriaco A. Piccirillo
4Department of Microbiology, Department of Immunology, and Center for the Study of Host Resistance, McGill University, Montreal, Quebec H3A 2BA, Canada
Romina S. Goldszmid
2Immunobiology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD 20892
Yasmine Belkaid
1Mucosal Immunology Unit
3Division of Molecular Immunology, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229
CORRESPONDENCE Yasmine Belkaid: [email protected]
Abbreviations used: B/6, C57BL/6; BMDC, bone marrow–derived DC; T reg, regulatory T.
Received:
October 13 2005
Accepted:
February 10 2006
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2006
J Exp Med (2006) 203 (3): 777–788.
Article history
Received:
October 13 2005
Accepted:
February 10 2006
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Citation
Isabelle J. Suffia, Stacie K. Reckling, Ciriaco A. Piccirillo, Romina S. Goldszmid, Yasmine Belkaid; Infected site-restricted Foxp3+ natural regulatory T cells are specific for microbial antigens . J Exp Med 20 March 2006; 203 (3): 777–788. doi: https://doi.org/10.1084/jem.20052056
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