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Editorial: Methods in T cell biology: 2022

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URI: http://hdl.handle.net/10498/31473

DOI: 10.3389/FIMMU.2023.1266576

ISSN: 1664-3224

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OA_2023_0200.pdf (255.6Kb)
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Author/s
Aguado Vidal, EnriqueAuthority UCA; Call, M.E.
Date
2023
Department
Biomedicina, Biotecnología y Salud Pública
Source
Frontiers in Immunology
Abstract
T cells are crucial players of immune responses by their ability to specifically recognize foreign, potentially harmful, antigens. To perform such specific recognition, T cells express at their plasma membrane an antigen receptor called the T cell receptor (TCR) (1–3). The TCR expressed at the plasma membrane in the majority of T cells is composed by a TCR-a and TCR-b heterodimer, which is able to recognize a complex formed by an antigenic peptide coupled to an MHC molecule (pMHC complex). After specific recognition by a pMHC complex the TCR triggers multiple intracellular signals leading to proliferation, target cell killing, cytokine secretion, and differentiation into effector T cells. Although our understanding of the molecular mechanisms governing activation of T cells has dramatically grown in recent years, there is still much to learn
Subjects
binding prediction; machine learning; method; T cell; T cell epitope; TCR (T cell receptor)
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This work is under a Creative Commons License Atribución 4.0 Internacional

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