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PTPN2 phosphatase deletion in T cells promotes anti-tumour immunity and CAR T-cell efficacy in solid tumours.
- Source :
-
The EMBO journal [EMBO J] 2020 Jan 15; Vol. 39 (2), pp. e103637. Date of Electronic Publication: 2019 Dec 05. - Publication Year :
- 2020
-
Abstract
- Although adoptive T-cell therapy has shown remarkable clinical efficacy in haematological malignancies, its success in combating solid tumours has been limited. Here, we report that PTPN2 deletion in T cells enhances cancer immunosurveillance and the efficacy of adoptively transferred tumour-specific T cells. T-cell-specific PTPN2 deficiency prevented tumours forming in aged mice heterozygous for the tumour suppressor p53. Adoptive transfer of PTPN2-deficient CD8 <superscript>+</superscript> T cells markedly repressed tumour formation in mice bearing mammary tumours. Moreover, PTPN2 deletion in T cells expressing a chimeric antigen receptor (CAR) specific for the oncoprotein HER-2 increased the activation of the Src family kinase LCK and cytokine-induced STAT-5 signalling, thereby enhancing both CAR T-cell activation and homing to CXCL9/10-expressing tumours to eradicate HER-2 <superscript>+</superscript> mammary tumours in vivo. Our findings define PTPN2 as a target for bolstering T-cell-mediated anti-tumour immunity and CAR T-cell therapy against solid tumours.<br /> (© 2019 The Authors. Published under the terms of the CC BY 4.0 license.)
- Subjects :
- Adoptive Transfer
Animals
Antigen Presentation immunology
Female
Humans
Male
Mice
Mice, Knockout
Mice, Transgenic
Neoplasms genetics
Neoplasms immunology
Signal Transduction
CD8-Positive T-Lymphocytes immunology
Immunotherapy, Adoptive methods
Lymphocyte Activation immunology
Neoplasms therapy
Protein Tyrosine Phosphatase, Non-Receptor Type 2 physiology
Receptor, ErbB-2 physiology
Receptors, Antigen, T-Cell immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1460-2075
- Volume :
- 39
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- The EMBO journal
- Publication Type :
- Academic Journal
- Accession number :
- 31803974
- Full Text :
- https://doi.org/10.15252/embj.2019103637