Perspective
Journal of Investigative Dermatology (2006) 126, 25–31. doi:10.1038/sj.jid.5700003
Immunosurveillance and Immunoregulation by 
T Cells
Michael Girardi1
1Department of Dermatology, Yale University School of Medicine, New Haven, Connecticut, USA
Correspondence: Dr Michael Girardi, Associate Professor and Residency Director, Department of Dermatology, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06520-8059, USA. Email: michael.girardi@yale.edu
Received 20 June 2005; Revised 19 August 2005; Accepted 2 September 2005.
Abstract
Whereas the vast majority of T cells express a T-cell receptor (TCR) composed of 
heterodimers, a smaller population expresses a 
TCR. In contrast to 
T cells, 
T cells show less TCR diversity, are particularly enriched at epithelial surfaces and appear to respond to self-molecules that signal potential danger or cellular stress. In addition, various subsets of 
T cells have shown antitumor and immunoregulatory activities. This review considers what has been discovered about the important cutaneous functions of 
T cells through the study of mutant mice and offers perspectives on the roles of 
T cells in human disease.
Abbreviations:
CDR3, complementarity-determining region 3; D, diversity (region); DETC, dendritic epidermal T cell; IEL, intraepithelial lymphocyte; J, junctional (region); MHC, major histocompatibility complex; MICA, major histocompatibility complex class I chain-related A; MICB, major histocompatibility complex class I chain-related B; NK, natural killer; NKT, natural killer T (cell); Rae-1, retinoic acid early-1; V, variable (region).
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