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作 者:张子明 柴国静 宋淑霞[1] ZHANG Zi-Ming;CHAI Guo-Jing;SONG Shu-Xia(Department of Immunology,Hebei Medical University,Key Laboratory of Immune Mechanism and Intervention on Serious Disease in Hebei Province,Shijiazuhang 050017,China)
机构地区:[1]河北医科大学免疫教研室河北省重大疾病免疫机制及干预实验室,石家庄050017 [2]河北省人民医院检验科,石家庄050000
出 处:《中国免疫学杂志》2019年第8期1018-1023,共6页Chinese Journal of Immunology
基 金:国家自然科学基金(81071710);河北省自然科学基金(H2014206180);河北省高等学校科学技术研究重点项目(ZD2017049)资助项目
摘 要:可塑性和多样性是巨噬细胞的重要特征,根据其功能不同,巨噬细胞被分为经典活化型即M1型,替代活化型即M2型。诱导M1和M2型巨噬细胞分化的条件不同,M1和M2型巨噬细胞的表型及功能也存在差异。在多数肿瘤微环境中存在M2型的巨噬细胞,该细胞通过产生多种细胞因子及蛋白酶参与肿瘤血管形成,并促进肿瘤的增殖及转移。因此,靶向抑制M2型巨噬细胞分化、清除M2型巨噬细胞等措施已成为肿瘤治疗研究的重要领域。本文主要对巨噬细胞的极化、肿瘤微环境对肿瘤相关巨噬细胞极化的影响及靶向肿瘤相关巨噬细胞的治疗策略进行综述。Plasticity and diversity are important characteristics of macrophages.According to their different functions,macrophages are classified into the classic activated type,M1 type,and the alternative activated type,M2 type.Not only the inducers for M1 and M2 macrophages differentiation were different,but the phenotypes and functions of M1 and M2 macrophages were different.M2 macrophages exist in most of the tumor microenvironment.Furthermore,the M2 type macrophages could secret many cytokines,chemokines and protease which involved in tumor angiogenesis,and promote the gowth and metastasis of tumor.Therefore,targeted inhibition of differentiation of M2-type macrophages and elimination of M2-type macrophages have become an important research area in tumor treatment.
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