Macrophages as a "weapon" in anticancer cellular immunotherapy

被引:51
作者
Aminin, Dmitry [1 ,2 ]
Wang, Yun-Ming [3 ,4 ]
机构
[1] GB Elyakov Pacific Inst Bioorgan Chem, Vladivostok, Russia
[2] Kaohsiung Med Univ, Kaohsiung, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Inst Mol Med & Bioengn, Dept Biol Sci & Technol, Ctr Intelligent Drug Syst & Smart Biodevices IDS2, Hsinchu, Taiwan
[4] Kaohsiung Med Univ, Ctr Canc Res, Dept Biomed Sci & Environm Biol, Kaohsiung, Taiwan
关键词
anticancer cellular immunotherapy; cancer; M1; phenotype; macrophages; TUMOR-ASSOCIATED MACROPHAGES; ADOPTIVE IMMUNOTHERAPY; TUMORICIDAL ACTIVITY; ANTITUMOR-ACTIVITY; MOUSE MACROPHAGES; BREAST-CANCER; IMMUNE CELLS; FC-GAMMA; ACTIVATION; THERAPY;
D O I
10.1002/kjm2.12405
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Anticancer immunotherapy is a treatment that activates the immune system to fight the tumor. Immunotherapy has several advantages over other cancer treatments in that anticancer immunotherapy displays high specificity, low side effects, and can combine with various conventional therapies. In recent years, oncologists have shown increasing interest in using macrophages for adoptive cell therapy and predict a bright future of macrophage-directed therapy for eliminating cancer. The focus of increased research interest is the classically activated M1 macrophages exhibiting pronounced tumoricidal activity, and the alternatively activated M2 tumor-associated macrophages, which otherwise help malignant cells evading attack by the immune system. M1 macrophages may represent an effective weapon in anticancer cellular immunotherapy, and the use of autoimmune macrophages properly prepared for antitumor administration is one of the promising ways for personalized therapy of cancer patients. The present report mainly discusses some modern aspects of the problem in application of activated M1 macrophage in anticancer therapy and reviews relevant publications up to 2021.
引用
收藏
页码:749 / 758
页数:10
相关论文
共 92 条
[1]   Clinical Cancer Therapy by NK Cells via Antibody-Dependent Cell-Mediated Cytotoxicity [J].
Alderson, Kory L. ;
Sondel, Paul M. .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2011,
[2]  
Alvey C., 2017, THESIS, V2164
[3]   SIRPA-Inhibited, Marrow-Derived Macrophages Engorge, Accumulate, and Differentiate in Antibody-Targeted Regression of Solid Tumors [J].
Alvey, Cory M. ;
Spinler, Kyle R. ;
Irianto, Jerome ;
Pfeifer, Charlotte R. ;
Hayes, Brandon ;
Xia, Yuntao ;
Cho, Sangkyun ;
Dingal, P. C. P. Dave ;
Hsu, Jake ;
Smith, Lucas ;
Tewari, Manu ;
Discher, Dennis E. .
CURRENT BIOLOGY, 2017, 27 (14) :2065-+
[4]  
Aminin D., 2014, MARINE FRESHWATER TO, P1, DOI [10.1007/978-94-007-6650-1_3-1, DOI 10.1007/978-94-007-6650-1_3-1]
[5]   Glycosides from edible sea cucumbers stimulate macrophages via purinergic receptors [J].
Aminin, Dmitry ;
Pislyagin, Evgeny ;
Astashev, Maxim ;
Es'kov, Andrey ;
Kozhemyako, Valery ;
Avilov, Sergei ;
Zelepuga, Elena ;
Yurchenko, Ekaterina ;
Kaluzhskiy, Leonid ;
Kozlovskaya, Emma ;
Ivanov, Alexis ;
Stonik, Valentin .
SCIENTIFIC REPORTS, 2016, 6
[6]   Monocyte-mediated delivery of polymeric backpacks to inflamed tissues: a generalized strategy to deliver drugs to treat inflammation [J].
Anselmo, Aaron C. ;
Gilbert, Jonathan B. ;
Kumar, Sunny ;
Gupta, Vivek ;
Cohen, Robert E. ;
Rubner, Michael F. ;
Mitragotri, Samir .
JOURNAL OF CONTROLLED RELEASE, 2015, 199 :29-36
[7]   CD24 signalling through macrophage Siglec-10 is a target for cancer immunotherapy [J].
Barkal, Amira A. ;
Brewer, Rachel E. ;
Markovic, Maxim ;
Kowarsky, Mark ;
Barkal, Sammy A. ;
Zaro, Balyn W. ;
Krishnan, Venkatesh ;
Hatakeyama, Jason ;
Dorigo, Oliver ;
Barkal, Layla J. ;
Weissman, Irving L. .
NATURE, 2019, 572 (7769) :392-+
[8]   Engagement of MHC class I by the inhibitory receptor LILRB1 suppresses macrophages and is a target of cancer immunotherapy [J].
Barkal, Amira A. ;
Weiskopf, Kipp ;
Kao, Kevin S. ;
Gordon, Sydney R. ;
Rosental, Benyamin ;
Yiu, Ying Y. ;
George, Benson M. ;
Markovic, Maxim ;
Ring, Nan G. ;
Tsai, Jonathan M. ;
McKenna, Kelly M. ;
Ho, Po Yi ;
Cheng, Robin Z. ;
Chen, James Y. ;
Barkal, Layla J. ;
Ring, Aaron M. ;
Weissman, Irving L. ;
Maute, Roy L. .
NATURE IMMUNOLOGY, 2018, 19 (01) :76-+
[9]   Chimeric antigen receptor-modified T cells for the treatment of solid tumors: Defining the challenges and next steps [J].
Beatty, Gregory L. ;
O'Hara, Mark .
PHARMACOLOGY & THERAPEUTICS, 2016, 166 :30-39
[10]   THE CYTO-TOXIC EFFECT OF MOUSE MACROPHAGES STIMULATED INVITRO BY A BETA-1,3-D-GLUCAN FROM YEAST-CELL WALLS [J].
BOGWALD, J ;
JOHNSON, E ;
SELJELID, R .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1982, 15 (03) :297-304