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Enhanced antitumor immunity by a novel small molecule HPK1 inhibitor

免疫系统 免疫检查点 癌症研究 肿瘤微环境 癌症免疫疗法 免疫疗法 生物 离体 T细胞受体 医学 免疫学 T细胞 体内 生物技术
作者
Dan You,Stephen Hillerman,Gregory Locke,Charu Chaudhry,Caitlyn Stromko,Anwar Murtaza,Yi Fan,Jennifer Koenitzer,Yali Chen,Stephanie W. Briceno,Rajarshi Bhadra,Elizabeth K. Duperret,Johnni Gullo-Brown,Chan Gao,Dandan Zhao,John N. Feder,Joshua C. Curtin,Andrew P. Degnan,Godwin Kumi,Mark D. Wittman,Benjamin M. Johnson,Karen E. Parrish,Giridharan Gokulrangan,J. S. Morrison,Michael Quigley,John T. Hunt,Luisa Salter–Cid,Emma Lees,Miguel A. F. Sanjuán,Jinqi Liu
出处
期刊:Journal for ImmunoTherapy of Cancer [BMJ]
卷期号:9 (1): e001402-e001402 被引量:56
标识
DOI:10.1136/jitc-2020-001402
摘要

Hematopoietic progenitor kinase 1 (HPK1 or MAP4K1) has been demonstrated as a negative intracellular immune checkpoint in mediating antitumor immunity in studies with HPK1 knockout and kinase dead mice. Pharmacological inhibition of HPK1 is desirable to investigate the role of HPK1 in human immune cells with therapeutic implications. However, a significant challenge remains to identify a small molecule inhibitor of HPK1 with sufficient potency, selectivity, and other drug-like properties suitable for proof-of-concept studies. In this report, we identified a novel, potent, and selective HPK1 small molecule kinase inhibitor, compound K (CompK). A series of studies were conducted to investigate the mechanism of action of CompK, aiming to understand its potential application in cancer immunotherapy.Human primary T cells and dendritic cells (DCs) were investigated with CompK treatment under conditions relevant to tumor microenvironment (TME). Syngeneic tumor models were used to assess the in vivo pharmacology of CompK followed by human tumor interrogation ex vivo.CompK treatment demonstrated markedly enhanced human T-cell immune responses under immunosuppressive conditions relevant to the TME and an increased avidity of the T-cell receptor (TCR) to recognize viral and tumor-associated antigens (TAAs) in significant synergy with anti-PD1. Animal model studies, including 1956 sarcoma and MC38 syngeneic models, revealed improved immune responses and superb antitumor efficacy in combination of CompK with anti-PD-1. An elevated immune response induced by CompK was observed with fresh tumor samples from multiple patients with colorectal carcinoma, suggesting a mechanistic translation from mouse model to human disease.CompK treatment significantly improved human T-cell functions, with enhanced TCR avidity to recognize TAAs and tumor cytolytic activity by CD8+ T cells. Additional benefits include DC maturation and priming facilitation in tumor draining lymph node. CompK represents a novel pharmacological agent to address cancer treatment resistance.
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