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用鼠抗白细胞介素-6单克隆抗体治疗一名浆细胞白血病患者。

Murine anti-interleukin-6 monoclonal antibody therapy for a patient with plasma cell leukemia.

作者信息

Klein B, Wijdenes J, Zhang X G, Jourdan M, Boiron J M, Brochier J, Liautard J, Merlin M, Clement C, Morel-Fournier B

机构信息

INSERM U291, Montpellier, France.

出版信息

Blood. 1991 Sep 1;78(5):1198-204.

PMID:1715218
Abstract

A patient with primary plasma cell leukemia resistant to chemotherapy was treated for 2 months with daily intravenous injections of anti-interleukin-6 (IL-6) monoclonal antibodies (MoAbs). The patient's clinical status improved throughout the treatment and no major side effects were observed. Serial monitoring showed blockage of the myeloma cell proliferation in the bone marrow (from 4.5% to 0% myeloma cells in the S-phase in vivo) as well as reduction in the serum calcium, serum monoclonal IgG, and the serum C-reactive protein levels. The serum calcium and serum monoclonal IgG corrected by approximately 30%, whereas the C-reactive protein corrected to undetectable levels during treatment. No major side effects developed, although both platelet and circulating neutrophil counts decreased during anti-IL-6 therapy. A transient immunization was detected 15 days after the initiation of the treatment, which could explain the recovery of myeloma cell proliferation after 2 months of treatment (2% myeloma cells in the S phase). In conclusion, this first anti-IL-6 clinical trial demonstrated the feasibility of injecting anti-IL-6 MoAbs, and also a transient tumor cytostasis and a reduction in IL-6-related toxicities. It gave insight into the major biologic activities of IL-6 in vivo and may serve as a basis for further development of anti-IL-6 therapy in myeloma and other IL-6-related diseases.

摘要

一名对化疗耐药的原发性浆细胞白血病患者接受了为期2个月的每日静脉注射抗白细胞介素-6(IL-6)单克隆抗体(MoAbs)治疗。在整个治疗过程中,患者的临床状况有所改善,未观察到重大副作用。连续监测显示骨髓中骨髓瘤细胞增殖受到阻滞(体内S期骨髓瘤细胞从4.5%降至0%),同时血清钙、血清单克隆IgG和血清C反应蛋白水平降低。血清钙和血清单克隆IgG校正了约30%,而C反应蛋白在治疗期间校正至检测不到的水平。尽管在抗IL-6治疗期间血小板和循环中性粒细胞计数均下降,但未出现重大副作用。治疗开始15天后检测到短暂的免疫反应,这可以解释治疗2个月后骨髓瘤细胞增殖的恢复(S期骨髓瘤细胞为2%)。总之,这项首次抗IL-6临床试验证明了注射抗IL-6 MoAbs的可行性,以及短暂的肿瘤细胞生长停滞和IL-6相关毒性的降低。它深入了解了IL-6在体内的主要生物学活性,并可能为骨髓瘤和其他IL-6相关疾病的抗IL-6治疗的进一步发展奠定基础。

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