化疗后肿瘤患者外周血树突状细胞计数及功能的恢复。

S. Markowicz, J. Walewski, K. Zajda, P. Wiechno, H. Skurzak, J. Giermek, A. Gajkowska, M. Krzakowski, T. Pienkowski
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引用次数: 8

摘要

对淋巴瘤和实体瘤患者化疗前后外周血树突状细胞(DC)计数及功能进行了检测。化疗开始后第一周DC计数明显下降,第二周恢复,第三周超过基线值。化疗第一个周期和最后一个周期后的DC恢复通常相似。DC1和DC2亚群遵循整个DC人群的重构模式。单核细胞和粒细胞恢复时间比DC晚1 ~ 2周。对完全依赖DC的keyhole淋巴血青素(KLH)的原发性增殖反应在化疗开始后的第一周内下降,大多数患者(包括最初无反应的患者)随DC计数恢复。淋巴瘤和部分实体瘤患者化疗结束时,KLH应答性恢复,但抗cd3抗体应答性未恢复。在接受多周期化疗的淋巴瘤患者中,CD4+ T细胞的长期耗竭可能导致反应性丧失。然而,在一些实体瘤患者中,尽管DC和CD4+ t细胞计数都有重建,但对KLH的反应性不存在。我们的数据表明,DC的数值重构不一定伴随着功能恢复。在设计DC收集方案时应考虑DC的早期恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recovery of dendritic cell counts and function in peripheral blood of cancer patients after chemotherapy.
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.
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