Roles of tumor-associated macrophages in anti-PD-1/PD-L1 immunotherapy for solid cancers

被引:255
作者
Zhang, Hao [1 ]
Liu, Lin [2 ,3 ]
Liu, Jinbo [1 ]
Dang, Pengyuan [1 ]
Hu, Shengyun [1 ]
Yuan, Weitang [1 ]
Sun, Zhenqiang [1 ,2 ]
Liu, Yang [4 ]
Wang, Chengzeng [2 ,3 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Colorectal Surg, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Henan Inst Interconnected Intelligent Hlth Managem, Zhengzhou 450052, Henan, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Dept Ultrasound, Zhengzhou 450052, Henan, Peoples R China
[4] Zhengzhou Univ, Affiliated Canc Hosp, Henan Canc Hosp, Dept Radiotherapy, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
Tumor-associated macrophages; Immune checkpoint inhibitors; Cancer; Combined therapy; NEGATIVE BREAST-CANCER; HEPATOCELLULAR-CARCINOMA; ADAPTIVE IMMUNITY; EPIGENETIC REGULATION; MOLECULAR-MECHANISMS; ACQUIRED-RESISTANCE; ANTITUMOR IMMUNITY; DISTINCT SUBSETS; PD-1; EXPRESSION; NONCODING RNAS;
D O I
10.1186/s12943-023-01725-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
In recent years, tumor immunotherapy has made significant progress. However, tumor immunotherapy, particularly immune checkpoint inhibitors (e.g., PD-1/PD-L1 inhibitors), benefits only a tiny proportion of patients in solid cancers. The tumor microenvironment (TME) acts a significant role in tumor immunotherapy. Studies reported that tumor-associated macrophages (TAMs), as one of the main components of TME, seriously affected the therapeutic effect of PD-1/PD-L1 inhibitors. In this review, we analyzed TAMs from epigenetic and single-cell perspectives and introduced the role and mechanisms of TAMs in anti-programmed death protein 1(anti-PD-1) therapy. In addition, we summarized combination regimens that enhance the efficacy of tumor PD-1/PD-L1 inhibitors and elaborated on the role of the TAMs in different solid cancers. Eventually, the clinical value of TAMs by influencing the therapeutic effect of tumor PD-1/PD-L1 inhibitors was discussed. These above are beneficial to elucidate poor therapeutic effect of PD-1/PD-L1 inhibitors in solid tumors from the point of view of TAMs and explore the strategies to improve its objective remission rate of solid cancers.
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页数:23
相关论文
共 222 条
[1]
Melanoma brain metastases treated with stereotactic radiosurgery and concurrent pembrolizumab display marked regression; efficacy and safety of combined treatment [J].
Anderson, Erik S. ;
Postow, Michael A. ;
Wolchok, Jedd D. ;
Young, Robert J. ;
Ballangrud, Ase ;
Chan, Timothy A. ;
Yamada, Yoshiya ;
Beal, Kathryn .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2017, 5
[2]
Single-cell profiling of myeloid cells in glioblastoma across species and disease stage reveals macrophage competition and specialization [J].
Antunes, Ana Rita Pombo ;
Scheyltjens, Isabelle ;
Lodi, Francesca ;
Messiaen, Julie ;
Antoranz, Asier ;
Duerinck, Johnny ;
Kancheva, Daliya ;
Martens, Liesbet ;
De Vlaminck, Karen ;
Van Hove, Hannah ;
Hansen, Signe Schmidt Kjolner ;
Bosisio, Francesca Maria ;
Van der Borght, Koen ;
De Vleeschouwer, Steven ;
Sciot, Raf ;
Bouwens, Luc ;
Verfaillie, Michiel ;
Vandamme, Niels ;
Vandenbroucke, Roosmarijn E. ;
De Wever, Olivier ;
Saeys, Yvan ;
Guilliams, Martin ;
Gysemans, Conny ;
Neyns, Bart ;
De Smet, Frederik ;
Lambrechts, Diether ;
Van Ginderachter, Jo A. ;
Movahedi, Kiavash .
NATURE NEUROSCIENCE, 2021, 24 (04) :595-610
[3]
Combining immunotherapy and anticancer agents: the right path to achieve cancer cure? [J].
Apetoh, L. ;
Ladoire, S. ;
Coukos, G. ;
Ghiringhelli, F. .
ANNALS OF ONCOLOGY, 2015, 26 (09) :1813-1823
[4]
Arg1 expression defines immunosuppressive subsets of tumor-associated macrophages [J].
Arlauckas, Sean P. ;
Garren, Seth B. ;
Garris, Chris S. ;
Kohler, Rainer H. ;
Oh, Juhyun ;
Pittet, Mikael J. ;
Weissleder, Ralph .
THERANOSTICS, 2018, 8 (21) :5842-5854
[5]
In vivo imaging reveals a tumor-associated macrophage-mediated resistance pathway in anti-PD-1 therapy [J].
Arlauckas, Sean P. ;
Garris, Christopher S. ;
Kohler, Rainer H. ;
Kitaoka, Maya ;
Cuccarese, Michael F. ;
Yang, Katherine S. ;
Miller, Miles A. ;
Carlson, Jonathan C. ;
Freeman, Gordon J. ;
Anthony, Robert M. ;
Weissleder, Ralph ;
Pittet, Mikael J. .
SCIENCE TRANSLATIONAL MEDICINE, 2017, 9 (389)
[6]
Single-Cell Map of Diverse Immune Phenotypes in the Breast Tumor Microenvironment [J].
Azizi, Elham ;
Carr, Ambrose J. ;
Plitas, George ;
Cornish, Andrew E. ;
Konopacki, Catherine ;
Prabhakaran, Sandhya ;
Nainys, Juozas ;
Wu, Kenmin ;
Kiseliovas, Vaidotas ;
Setty, Manu ;
Choi, Kristy ;
Fromme, Rachel M. ;
Phuong Dao ;
McKenney, Peter T. ;
Wasti, Ruby C. ;
Kadaveru, Krishna ;
Mazutis, Linas ;
Rudensky, Alexander Y. ;
Pe'er, Dana .
CELL, 2018, 174 (05) :1293-+
[7]
A Mechanism of Hypoxia-Mediated Escape from Adaptive Immunity in Cancer Cells [J].
Barsoum, Ivraym B. ;
Smallwood, Chelsea A. ;
Siemens, D. Robert ;
Graham, Charles H. .
CANCER RESEARCH, 2014, 74 (03) :665-674
[8]
MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[9]
Baselga J, 2001, EUR J CANCER, V37, pS16
[10]
Innate immune cells in cirrhosis [J].
Bernsmeier, Christine ;
van der Merwe, Schalk ;
Perianin, Axel .
JOURNAL OF HEPATOLOGY, 2020, 73 (01) :186-201