Wieckowski Eva, Whiteside Theresa L
Departments of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Immunol Res. 2006;36(1-3):247-54. doi: 10.1385/IR:36:1:247.
Microvesicles (MV) or exosomes are produced and secreted by tumor and normal cells. The molecular profile and functions of tumor-derived vs dendritic cell (DC)-derived MV are distinct. The former express death ligands and mediate apoptosis of activated T cells. The latter promote CD4+ T cell proliferation and may play a role in regulating T cell responses. Serving as intercellular communication networks, tumor-derived MV contribute to tumor escape, while DC-derived MV drive and regulate immune response.
微泡(MV)或外泌体由肿瘤细胞和正常细胞产生并分泌。肿瘤来源的MV与树突状细胞(DC)来源的MV在分子特征和功能上有所不同。前者表达死亡配体并介导活化T细胞的凋亡。后者促进CD4+ T细胞增殖,并可能在调节T细胞反应中发挥作用。作为细胞间通讯网络,肿瘤来源的MV有助于肿瘤逃逸,而DC来源的MV驱动并调节免疫反应。