Regulation of T Helper Cell Fate by TCR Signal Strength.
Full text not available from this repository.Item Type: | Review |
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Status: | Published |
Official URL: | https://doi.org/10.3389/fimmu.2020.00624 |
Journal or Publication Title: | Frontiers in Immunology |
Volume: | 11 |
Date: | 2020 |
Divisions: | Tuberculosis |
Depositing User: | General Admin |
Identification Number: | 10.3389/fimmu.2020.00624 |
ISSN: | 1664-3224 |
Date Deposited: | 22 Dec 2020 03:24 |
Abstract: | T cells are critical in orchestrating protective immune responses to cancer and an array of pathogens. The interaction between a peptide MHC (pMHC) complex on antigen presenting cells (APCs) and T cell receptors (TCRs) on T cells initiates T cell activation, division, and clonal expansion in secondary lymphoid organs. T cells must also integrate multiple T cell-intrinsic and extrinsic signals to acquire the effector functions essential for the defense against invading microbes. In the case of T helper cell differentiation, while innate cytokines have been demonstrated to shape effector CD4+ T lymphocyte function, the contribution of TCR signaling strength to T helper cell differentiation is less understood. In this review, we summarize the signaling cascades regulated by the strength of TCR stimulation. Various mechanisms in which TCR signal strength controls T helper cell expansion and differentiation are also discussed. |
Creators: | Creators Email Bhattacharyya, Nayan D. UNSPECIFIED Feng, Carl G. UNSPECIFIED |
Last Modified: | 05 Jan 2021 12:00 |
URI: | https://eprints.centenary.org.au/id/eprint/895 |
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