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Becoming aware of γδ T cells.
Born, Willi K; O'Brien, Rebecca L.
Afiliación
  • Born WK; Department of Immunology and Genomic Medicine, National Jewish Health, Denver, CO, United States. Electronic address: bornw@njhealth.org.
  • O'Brien RL; Department of Immunology and Genomic Medicine, National Jewish Health, Denver, CO, United States; Department of Immunology and Microbiology, University of Colorado Health Sciences Center, Aurora, CO, United States.
Adv Immunol ; 153: 91-117, 2022.
Article en En | MEDLINE | ID: mdl-35469596
ABSTRACT
The discovery that B cells and αß T cells exist was predictable These cells gave themselves away through their products and biological effects. In contrast, there was no reason to anticipate the existence of γδ T cells. Even the accidental discovery of a novel TCR-like gene (later named γ) that did not encode TCR α or ß proteins did not immediately change this. TCR-like γ had no obvious function, and its early expression in the thymus encouraged speculation about a possible role in αß T cell development. However, the identification of human PBL-derived cell-lines which expressed CD3 in complex with the TCR-like γ protein, but not the αß TCR, first indicated that a second T cell-type might exist, and the TCR-like γ chain was observed to co-precipitate with another protein. Amid speculation about a possible second TCR, this potential dimeric partner was named δ. To determine if the δ protein was indeed TCR-like, we undertook to sequence it. Meanwhile, a fourth TCR-like gene was discovered and provisionally named x. TCR-like x had revealed itself through genomic rearrangements early in T cell development, and was an attractive candidate for the gene encoding δ. The observation that δ protein sequences matched the predicted amino acid sequences encoded by the x gene, as well as serological cross-reactivity, confirmed that the TCR-like x gene indeed encoded the δ protein. Thus, the γδ heterodimer was established as a second TCR, and the cells that express it (the γδ T cells) consequently represented a third lymphocyte-population with the potential of recognizing diverse antigens. Soon, it became clear that γδ T cells are widely distributed and conserved among the vertebrate species, implying biological importance. Consistently, early functional studies revealed their roles in host resistance to pathogens, tissue repair, immune regulation, metabolism, organ physiology and more. Albeit discovered late, γδ T cells have repeatedly proven to play a distinct and often critical immunological role, and now generate much interest.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de Antígenos de Linfocitos T gamma-delta / Receptores de Antígenos de Linfocitos T alfa-beta Límite: Animals / Humans Idioma: En Revista: Adv Immunol Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de Antígenos de Linfocitos T gamma-delta / Receptores de Antígenos de Linfocitos T alfa-beta Límite: Animals / Humans Idioma: En Revista: Adv Immunol Año: 2022 Tipo del documento: Article