Chair of Immunology, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University of Torun, Bydgoszcz, Poland.
Mediators Inflamm. 2013;2013:831387. doi: 10.1155/2013/831387. Epub 2013 Mar 17.
Due to the profile of released mediators (such as cytokines, chemokines, growth factors, etc.), neoplastic cells modulate the activity of immune system, directly affecting its components both locally and peripherally. This is reflected by the limited antineoplastic activity of the immune system (immunosuppressive effect), induction of tolerance to neoplastic antigens, and the promotion of processes associated with the proliferation of neoplastic tissue. Most of these responses are macrophages dependent, since these cells show proangiogenic properties, attenuate the adaptive response (anergization of naïve T lymphocytes, induction of Treg cell formation, polarization of immune response towards Th2, etc.), and support invasion and metastases formation. Tumor-associated macrophages (TAMs), a predominant component of leukocytic infiltrate, "cooperate" with the neoplastic tissue, leading to the intensified proliferation and the immune escape of the latter. This paper characterizes the function of macrophages in the development of neoplastic disease.
由于释放介质(如细胞因子、趋化因子、生长因子等)的特征,肿瘤细胞调节免疫系统的活性,直接影响其局部和外周的成分。这反映在免疫系统的抗肿瘤活性有限(免疫抑制作用)、诱导对肿瘤抗原的耐受以及促进与肿瘤组织增殖相关的过程。这些反应大多依赖于巨噬细胞,因为这些细胞具有促血管生成特性,减弱适应性反应(幼稚 T 淋巴细胞的失能、诱导 Treg 细胞形成、免疫应答向 Th2 的极化等),并支持浸润和转移的形成。肿瘤相关巨噬细胞(TAMs)是白细胞浸润的主要成分之一,与肿瘤组织“合作”,导致后者的增殖和免疫逃逸加剧。本文描述了巨噬细胞在肿瘤疾病发展中的作用。