PD-1 Blockade on Tumor Microenvironment-Resident ILC2s Promotes TNF-α Production and Restricts Progression of Metastatic Melanoma

被引:20
作者
Howard, Emily [1 ]
Hurrell, Benjamin P. [1 ]
Helou, Doumet Georges [1 ]
Quach, Christine [1 ]
Painter, Jacob D. [1 ]
Shafiei-Jahani, Pedram [1 ]
Fung, Marshall [1 ]
Gill, Parkash S. [2 ]
Soroosh, Pejman [3 ]
Sharpe, Arlene H. [4 ]
Akbari, Omid [1 ,2 ]
机构
[1] Univ Southern Calif, Keck Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA 90007 USA
[2] Univ Southern Calif, Norris Canc Ctr, Keck Sch Med, Dept Med, Los Angeles, CA 90007 USA
[3] Janssen Res & Dev, Immunometab, San Diego, CA USA
[4] Harvard Med Sch, Dept Immunol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
innate lymphoid cell 2; cancer; melanoma; PD-1; TNF-alpha; LYMPHOID-CELL FUNCTION; INFLAMMATION; INDUCTION; REGULATOR;
D O I
10.3389/fimmu.2021.733136
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
While pulmonary ILC2s represent one of the major tissue-resident innate lymphoid cell populations at steady state and are key drivers of cytokine secretion in their occupational niche, their role in pulmonary cancer progression remains unclear. As the programmed cell death protein-1 (PD-1) plays a major role in cancer immunotherapy and immunoregulatory properties, here we investigate the specific effect of PD-1 inhibition on ILC2s during pulmonary B16 melanoma cancer metastasis. We demonstrate that PD-1 inhibition on ILC2s suppresses B16 tumor growth. Further, PD-1 inhibition upregulates pulmonary ILC2-derived TNF-alpha production, a cytotoxic cytokine that directly induces cell death in B16 cells, independent of adaptive immunity. Together, these results highlight the importance of ILC2s and their anti-tumor role in pulmonary B16 cancer progression during PD-1 inhibitory immunotherapy.
引用
收藏
页数:12
相关论文
共 40 条
[1]   Molecular mechanisms of IL-33-mediated stromal interactions in cancer metastasis [J].
Andersson, Patrik ;
Yang, Yunlong ;
Hosaka, Kayoko ;
Zhang, Yin ;
Fischer, Carina ;
Braun, Harald ;
Liu, Shuzhen ;
Yu, Guohua ;
Liu, Shihai ;
Beyaert, Rudi ;
Chang, Mayland ;
Li, Qi ;
Cao, Yihai .
JCI INSIGHT, 2018, 3 (20)
[2]  
Atallah Ehab, 2005, Curr Treat Options Oncol, V6, P185
[3]   IL-1β, IL-4 and IL-12 control the fate of group 2 innate lymphoid cells in human airway inflammation in the lungs [J].
Bal, Suzanne M. ;
Bernink, Jochem H. ;
Nagasawa, Maho ;
Groot, Jelle ;
Shikhagaie, Medya M. ;
Golebski, Kornel ;
van Drunen, Cornelis M. ;
Lutter, Rene ;
Jonkers, Rene E. ;
Hombrink, Pleun ;
Bruchard, Melanie ;
Villaudy, Julien ;
Munneke, J. Marius ;
Fokkens, Wytske ;
Erjefalt, Jonas S. ;
Spits, Hergen ;
Ros, Xavier Romero .
NATURE IMMUNOLOGY, 2016, 17 (06) :636-+
[4]   Targeting TNF-α to Neoangiogenic Vessels Enhances Lymphocyte Infiltration in Tumors and Increases the Therapeutic Potential of Immunotherapy [J].
Calcinotto, Arianna ;
Grioni, Matteo ;
Jachetti, Elena ;
Curnis, Flavio ;
Mondino, Anna ;
Parmiani, Giorgio ;
Corti, Angelo ;
Bellone, Matteo .
JOURNAL OF IMMUNOLOGY, 2012, 188 (06) :2687-2694
[5]   Targeting Tumor Vasculature with TNF Leads Effector T Cells to the Tumor and Enhances Therapeutic Efficacy of Immune Checkpoint Blockers in Combination with Adoptive Cell Therapy [J].
Elia, Angela Rita ;
Grioni, Matteo ;
Basso, Veronica ;
Curnis, Flavio ;
Freschi, Massimo ;
Corti, Angelo ;
Mondino, Anna ;
Bellone, Matteo .
CLINICAL CANCER RESEARCH, 2018, 24 (09) :2171-2181
[6]   IL-1β, IL-23, and TGF-β drive plasticity of human ILC2s towards IL-17-producing ILCs in nasal inflammation [J].
Golebski, Korneliusz ;
Ros, Xavier R. ;
Nagasawa, Maho ;
van Tol, Sophie ;
Heesters, Balthasar A. ;
Aglmous, Hajar ;
Kradolfer, Chantal M. A. ;
Shikhagaie, Medya M. ;
Seys, Sven ;
Hellings, P. W. ;
van Drunen, Cornelis M. ;
Fokkens, Wytske J. ;
Spits, Hergen ;
Bal, Suzanne M. .
NATURE COMMUNICATIONS, 2019, 10 (1)
[7]   Alteration of Tumor Metabolism by CD4+T Cells Leads to TNF-α-Dependent Intensification of Oxidative Stress and Tumor Cell Death [J].
Habtetsion, Tsadik ;
Ding, Zhi-Chun ;
Pi, Wenhu ;
Li, Tao ;
Lu, Chunwan ;
Chen, Tingting ;
Xi, Caixia ;
Spartz, Helena ;
Liu, Kebin ;
Hao, Zhonglin ;
Mivechi, Nahid ;
Huo, Yuqing ;
Blazar, Bruce R. ;
Munn, David H. ;
Zhou, Gang .
CELL METABOLISM, 2018, 28 (02) :228-+
[8]   LAIR-1 acts as an immune checkpoint on activated ILC2s and regulates the induction of airway hyperreactivity [J].
Helou, Doumet Georges ;
Shafiei-Jahani, Pedram ;
Hurrell, Benjamin P. ;
Painter, Jacob D. ;
Quach, Christine ;
Howard, Emily ;
Akbari, Omid .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2022, 149 (01) :223-+
[9]   PD-1 pathway regulates ILC2 metabolism and PD-1 agonist treatment ameliorates airway hyperreactivity [J].
Helou, Doumet Georges ;
Shafiei-Jahani, Pedram ;
Lo, Richard ;
Howard, Emily ;
Hurrell, Benjamin P. ;
Galle-Treger, Lauriane ;
Painter, Jacob D. ;
Lewis, Gavin ;
Soroosh, Pejman ;
Sharpe, Arlene H. ;
Akbari, Omid .
NATURE COMMUNICATIONS, 2020, 11 (01)
[10]   IL-10 production by ILC2s requires Blimp-1 and cMaf, modulates cellular metabolism, and ameliorates airway hyperreactivity [J].
Howard, Emily ;
Lewis, Gavin ;
Galle-Treger, Lauriane ;
Hurrell, Benjamin P. ;
Helou, Doumet Georges ;
Shafiei-Jahani, Pedram ;
Painter, Jacob D. ;
Muench, German Aleman ;
Soroosh, Pejman ;
Akbari, Omid .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2021, 147 (04) :1281-+