免疫系统
鼻咽癌
免疫学
医学
免疫疗法
髓样
癌症研究
吉西他滨
CD14型
细胞毒性T细胞
白细胞介素2受体
化疗
T细胞
生物
内科学
放射治疗
体外
生物化学
作者
Xiaomin Li,Xiaomin Zhang,Junyan Li,Ning Jiang,Lei Chen,Ling‐Long Tang,Yan‐Ping Mao,Wen‐Fei Li,Guan-Qun Zhou,Ying‐Qin Li,Na Liu,Yuan Zhang,Jun Ma
摘要
Studies are trying to add immunotherapy to gemcitabine and cisplatin (GP) induction chemotherapy, the standard therapy, in nasopharyngeal carcinoma (NPC) patients with locoregionally advanced disease. However, how the immune system responds to GP remains unknown.We examined the dynamic changes of circulating immune cells and plasma cytokines in NPC patients administered with GP.After GP administration, immunosuppressive myeloid cells, including CD11b+CD14+ monocytes, CD33+ myeloid cells, CD33+CD11+ myeloid cells, total MDSCs (CD33+CD11+HLA-DR-/low), monocytic MDSCs, and granulocytic MDSCs decreased significantly. The regulatory T cells and B cells, two important suppressive lymphocyte subpopulations, also decreased. On the other hand, the levels of CD3+ T cells, total B cells, central memory CD4+ T cells, and pro-inflammatory cytokines (including Interleukin [IL]-1β, IL-6, IL-2, IL-5, and IL-8) increased significantly after GP administration. Besides, GP chemotherapy did not weaken the cytotoxic activity and proliferative capacity of T cells.Our results showed the immune modulation effect of GP induction chemotherapy in locoregionally advanced NPC, providing a solid basis for its combination with immunotherapy.
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