Author:
Wiede Florian,Lu Kun-Hui,Du Xin,Liang Shuwei,Hochheiser Katharina,Dodd Garron T.,Goh Pei,Kearney Conor,Meyran Deborah,Beavis Paul A.,Henderson Melissa A.,Park Simone L.,Waithman Jason,Zhang Sheng,Zhang Zhong-Yin,Oliaro Jane,Gebhardt Thomas,Darcy Phillip K.,Tiganis Tony
Abstract
ABSTRACTAlthough adoptive T cell therapy has shown remarkable clinical efficacy in hematological 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+ 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+ 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.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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