γδ T, NKT, and MAIT Cells During Evolution: Redundancy or Specialized Functions?

Author:

Harly Christelle12ORCID,Robert Jacques3ORCID,Legoux Francois4,Lantz Olivier456ORCID

Affiliation:

1. *Nantes Université, Institut National de la Santé et de la Recherche Médicale UMR1307, Centre National de la Recherche Scientifique UMR6075, Université d’Angers, Centre de Recherche en Cancérologie et Immunologie Intégrée Nantes Angers CRCI2NA, Nantes, France;

2. †LabEx Immunotherapy, Graft, Oncology, Nantes, France;

3. ‡Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY;

4. §INSERM U932, Paris Sciences et Lettres Université, Institut Curie, Paris, France;

5. ¶Laboratoire d’Immunologie Clinique, Institut Curie, Paris, France; and

6. ‖Centre d’Investigation Clinique en Biothérapie Gustave-Roussy Institut Curie (CIC-BT1428), Paris, France

Abstract

Abstract Innate-like T cells display characteristics of both innate lymphoid cells (ILCs) and mainstream αβ T cells, leading to overlapping functions of innate-like T cells with both subsets. In this review, we show that although innate-like T cells are probably present in all vertebrates, their main characteristics are much better known in amphibians and mammals. Innate-like T cells encompass both γδ and αβ T cells. In mammals, γδ TCRs likely coevolved with molecules of the butyrophilin family they interact with, whereas the semi-invariant TCRs of iNKT and mucosal-associated invariant T cells are evolutionarily locked with their restricting MH1b molecules, CD1d and MR1, respectively. The strong conservation of the Ag recognition systems of innate-like T cell subsets despite similar effector potentialities supports that each one fulfills nonredundant roles related to their Ag specificity.

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

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