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The Kinase Activity of Hematopoietic Progenitor Kinase 1 Is Essential for the Regulation of T Cell Function
Author(s) -
Sairy Hernandez,
Qing Jing,
Rebecca Hong Thibodeau,
Xiangnan Du,
Summer Park,
Hyang-Mi Lee,
Min Xu,
Soyoung Oh,
Armando Navarro,
Meron Roose-Girma,
Robert Newman,
Søren Warming,
Michelle Nannini,
Deepak Sampath,
Jeong Kim,
Jane L. Grogan,
Ira Mellman
Publication year - 2018
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2018.09.012
Subject(s) - biology , microbiology and biotechnology , t cell , cytotoxic t cell , lymphocytic choriomeningitis , cancer research , effector , cd8 , immune system , immunology , biochemistry , in vitro
We examined hematopoietic protein kinase 1 (HPK1), whose reliance on scaffold versus kinase functions for negative immune cell regulation is poorly understood and critical to its assessment as a viable drug target. We identify kinase-dependent roles for HPK1 in CD8 T cells that restrict their anti-viral and anti-tumor responses by using HPK1 kinase-dead (HPK1.kd) knockin mice. Loss of HPK1 kinase function enhanced T cell receptor signaling and cytokine secretion in a T-cell-intrinsic manner. In response to chronic lymphocytic choriomeningitis virus (LCMV) infection or tumor challenge, viral clearance and tumor growth inhibition were enhanced in HPK1.kd mice, accompanied by an increase in effector CD8 T cell function. Co-blockade of PD-L1 further enhanced T effector cell function, resulting in superior anti-viral and anti-tumor immunity over single target blockade. These results identify the importance of HPK1 kinase activity in the negative regulation of CD8 effector functions, implicating its potential as a cancer immunotherapy target.

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