4.6 Article

A critical role of costimulation during intrathymic development of invariant NK T cells

Journal

JOURNAL OF IMMUNOLOGY
Volume 180, Issue 4, Pages 2276-2283

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.180.4.2276

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Funding

  1. NIAID NIH HHS [R01 AI057485, R01 AI057485-04, AI 057485, AI 50746] Funding Source: Medline

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CD1d-restricted V alpha 14(+) invariant NK T (iNKT) cells are a specialized alpha beta T cell subset that regulates both innate and adaptive immunity. Although costimulatory molecules are required for the activation of conventional T cells and for the development of Foxp3(+) T cells, their role in iNKT cell regulation is unclear. Here we report that mice deficient in CD80/CD86 and/or B7h exhibit severe defects in thymic iNKT cell maturation, associated with largely reduced iNKT cell number in the thymus and the periphery. We show that costimulation is necessary for the optimal expansion of postselected NK1.1(-) immature iNKT cells in the thymus and for the proper expression of the maturation markers T-bet and CD122. Surprisingly, costimulatory molecules on both hemopoietic and nonhematopoietic cells are required for iNKT cell development. Our results thus demonstrate a previously unknown function of costimulation in the intrathymic development of iNKT cells, distinct from that of conventional T cells and regulatory T cells.

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