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Open AccessJournal ArticleDOI

gamma/delta and other unconventional T lymphocytes: what do they see and what do they do?

TLDR
These findings reveal that gamma/delta T cells and alpha/beta T cells recognize antigen in a fundamentally different way and hence mitigate the dogma of exclusive peptide-major histocompatibility complex recognition by T cells.
Abstract
T lymphocytes recognize specific ligands by clonally distributed T-cell receptors (TCR). In humans and most animals, the vast majority of T cells express a TCR composed of an alpha chain and a beta chain, whereas a minor T-cell population is characterized by the TCR gamma/delta. Almost all of our knowledge about T cells stems from alpha/beta T cells and only now are we beginning to understand gamma/delta T cells. In contrast to conventional alpha/beta T cells, which are specific for antigenic peptides presented by gene products of the major histocompatibility complex, gamma/delta T cells directly recognize proteins and even nonproteinacious phospholigands. These findings reveal that gamma/delta T cells and alpha/beta T cells recognize antigen in a fundamentally different way and hence mitigate the dogma of exclusive peptide-major histocompatibility complex recognition by T cells. A role for gamma/delta T cells in antimicrobial immunity has been firmly established. Although some gamma/delta T cells perform effector functions, regulation of the professional and the nonprofessional immune system seems to be of at least equal importance. The prominent residence of gamma/delta T cells in epithelial tissues and the rapid mobilization of gamma/delta T cells in response to infection are consistent with such regulatory activities under physiological and pathologic conditions. Thus, although gamma/delta T cells are a minor fraction of all T cells, they are not just uninfluential kin of alpha/beta T cells but have their unique raison d'etre.

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Of mice and not men: differences between mouse and human immunology

TL;DR: Known discrepancies in both innate and adaptive immunity are outlined, including balance of leukocyte subsets, defensins, Toll receptors, inducible NO synthase, the NK inhibitory receptor families Ly49 and KIR, FcR, Ig subsets andChemokine and chemokine receptor expression.
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[gamma][delta] cells: a right time and a right place for a conserved third way of protection.

TL;DR: The properties of g Mohammadelta cells form a basis for understanding gammadelta cell interactions with antigens and other cells that in turn form a based for understanding immunoprotective and regulatory functions of gammad delta cells in vivo.
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How can immunology contribute to the control of tuberculosis

TL;DR: A clear understanding of the immune responses that control the pathogen will be important for achieving optimal immunity, and information provided by functional genome analysis of M. tuberculosis will be vital in the design of a future vaccine.
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Innate Immunity to Mycobacterium tuberculosis

TL;DR: Different natural effector mechanisms for killing of M. tuberculosis have now been identified and these basic mechanisms augment the understanding of disease pathogenesis and clinical course and will be of help in designing adjunctive treatment strategies.
Journal ArticleDOI

Role of Heat Shock Proteins in Protection from and Pathogenesis of Infectious Diseases

TL;DR: An overview of the role of hsp in immunity with a focus on infectious and autoimmune diseases is provided.
References
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Journal ArticleDOI

The Envelope of Mycobacteria

TL;DR: Differences in mycolic acid structure may affect the fluidity and permeability of the bilayer, and may explain the different sensitivity levels of various mycobacterial species to lipophilic inhibitors.
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Tuberculosis: commentary on a reemergent killer.

TL;DR: The economic costs of not adequately addressing the problem of tuberculosis in this country are estimated from an epidemiological model.
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Adhesion between epithelial cells and T lymphocytes mediated by E-cadherin and the alpha E beta 7 integrin.

TL;DR: Heterotypic adhesive interactions between epithelial cells and intraepithelial lymphocytes in vitro are mediated by E-cadherin and the αEβ7 integrin, and are shown to mediated the tissue-specific compartmentalization of lymphocytes.
Journal ArticleDOI

Mutations in T-cell antigen receptor genes α and β block thymocyte development at different stages

TL;DR: Analysis of mice carrying mutant T-cell antigen receptor (TCP) genes indicates that TCP-β gene rearrangement or expression is critical for the differentiation of CD4− CD8− thymocyte to CD4+CD8+ thymocytes, as well as for the expansion of the pool ofCD4+ CD8+ cells.
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