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Recovery of dendritic cell counts and function in peripheral blood of cancer patients after chemotherapy.

机译:化疗后癌症患者外周血中树突状细胞计数和功能的恢复。

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Dendritic cell (DC) counts and function were assayed in peripheral blood of lymphoma and solid tumor patients before and after chemotherapy. The DC counts declined significantly within the first week from the start of chemotherapy, recovered in the second week, and exceeded the baseline values in the third week. DC recovery was usually similar after the first and after the last cycle of chemotherapy. DC1 and DC2 subsets followed the pattern of reconstitution found for the DC population as a whole. Monocytes and granulocytes recovered 1-2 weeks later than DC. The primary proliferative response to keyhole lympet hemocyanin (KLH), totally DC-dependent, declined within the first week from the start of chemotherapy, and in the majority of patients (including those initially unresponsive) recovered along with DC counts. The recovered responsiveness to KLH, but not to anti-CD3 antibody, disappeared at the end of chemotherapy in lymphoma and some solid tumor patients. Prolonged depletion of CD4+ T cells could contribute to the loss of responsiveness in lymphoma patients receiving multiple cycles of chemotherapy. However, in some solid tumor patients, the reactivity to KLH was absent, despite the reconstitution of both DC and CD4+ T-cell counts. Our data show that numerical reconstitution of DC is not necessarily accompanied by functional recovery. The early recovery of DC should be considered while designing protocols for DC collection for immunotherapy.
机译:在化疗前后,对淋巴瘤和实体瘤患者的外周血中树突状细胞(DC)的数量和功能进行了检测。从化疗开始的第一周,DC计数显着下降,第二周恢复,并在第三周超过基线值。在第一个化疗周期和最后一个化疗周期后,DC恢复通常相似。 DC1和DC2子集遵循整个DC人口发现的重构模式。单核细胞和粒细胞比DC恢复1-2周。完全DC依赖性的对匙孔血蓝蛋白(KLH)的主要增殖反应在化疗开始的第一周内下降,并且大多数患者(包括最初无反应的患者)与DC计数一起恢复。在淋巴瘤和一些实体瘤患者化疗结束时,对KLH而非对抗CD3抗体的恢复的反应性消失了。 CD4 + T细胞的长期耗竭可能会导致接受多个化疗周期的淋巴瘤患者反应性丧失。然而,在某些实体瘤患者中,尽管DC和CD4 + T细胞计数均得以重建,但对KLH的反应性却不存在。我们的数据表明,DC的数字重建不一定伴随着功能恢复。在设计用于免疫治疗的DC收集方案时,应考虑DC的早期恢复。

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