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OT-I TCR Transgenic Mice to Study the Role of PTPN22 in Anti-cancer Immunity.
Brownlie, Rebecca J; Zamoyska, Rose; Salmond, Robert J.
Afiliação
  • Brownlie RJ; Leeds Institute of Medical Research at St James's, University of Leeds, Wellcome Trust Brenner Building, St James's University Hospital, Leeds, UK.
  • Zamoyska R; Institute of Immunology and Infection Research, University of Edinburgh, Ashworth Laboratories, Edinburgh, UK.
  • Salmond RJ; Leeds Institute of Medical Research at St James's, University of Leeds, Wellcome Trust Brenner Building, St James's University Hospital, Leeds, UK. r.j.salmond@leeds.ac.uk.
Methods Mol Biol ; 2743: 81-92, 2024.
Article em En | MEDLINE | ID: mdl-38147209
ABSTRACT
Phosphotyrosine phosphatase non-receptor type 22 (PTPN22) is a key regulator of immune cell activation and responses. Genetic polymorphisms of PTPN22 have been strongly linked with an increased risk of developing autoimmune diseases, while analysis of PTPN22-deficient mouse strains has determined that PTPN22 serves as a negative regulator of T cell antigen receptor signaling. As well as these key roles in maintaining immune tolerance, PTPN22 acts as an intracellular checkpoint for T cell responses to cancer, suggesting that PTPN22 might be a useful target to improve T cell immunotherapies. To assess the potential for targeting PTPN22, we have crossed Ptpn22-deficient mice to an OT-I TCR transgenic background and used adoptive T cell transfer approaches in mouse cancer models. We provide basic methods for the in vitro expansion of effector OT-I cytotoxic T lymphocytes, in vitro phenotypic analysis, and in vivo adoptive T cell transfer models to assess the role of PTPN22 in anti-cancer immunity.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Antígenos de Linfócitos T / Neoplasias Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Antígenos de Linfócitos T / Neoplasias Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article