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[重组干扰素α治疗对慢性B型淋巴细胞白血病患者自然杀伤活性的影响]

[Effect of treatment with recombinant interferon alfa on natural killer activity in patients with chronic type B lymphatic leukemia].

作者信息

Villamor N, Montserrat E, Urbano-Ispízua A, Ribera J M, Rovira M, Vives Corrons J L, Rozman C

出版信息

Sangre (Barc). 1989 Dec;34(6):485-8.

PMID:2629126
Abstract

The role played by alpha interferon (alpha-IFN) in the treatment of B-type chronic lymphocytic leukaemia (B-CLL) has been studied by different authors. Despite the inconclusiveness of the results, alpha-IFN seems to be more effective in those patients with low tumour burden (early stages) who have been previously untreated. Although the mechanism of action of alpha-IFN is not wholly understood, it is known that this agent is a strong stimulant of the natural killer lymphocytes (NK). NK activity has been found decreased in B-CLL. In the present work the effect of alpha-IFN on NK activity was studied in 9 previously untreated B-CLL patients in stage A, who received chlorambucil (CLB) followed by alpha-IFN for at least 4 months. The disease stage did not change in most of the patients during alkylating or IFN therapy. CLB failed to increase NK activity, although it diminished the lymphocyte count. Although the lymphocyte count of the patients treated with alpha-IFN was not reduced beyond the values attained by CLB, NK activity reached normal values in 5 of the 7 patients in whom this was low, and kept within normal ranges in the two patients with normal NK activity. The number of CD57+ lymphocytes (this being the antigen present in NK cells) increased after alpha-IFN treatment, without any changes in the remaining T-lymphocyte (CD2, CD4 and CD8) and NK (CD16 and CD11b) subpopulations. These results show that alpha-IFN enhances NK activity in vivo.

摘要

不同作者研究了α干扰素(α-IFN)在B型慢性淋巴细胞白血病(B-CLL)治疗中所起的作用。尽管结果尚无定论,但α-IFN似乎对那些肿瘤负荷低(早期)且未接受过治疗的患者更有效。虽然α-IFN的作用机制尚未完全明了,但已知该药物是自然杀伤淋巴细胞(NK)的强效刺激剂。已发现B-CLL患者的NK活性降低。在本研究中,对9例A期未经治疗的B-CLL患者进行了研究,这些患者先接受苯丁酸氮芥(CLB)治疗,随后接受α-IFN治疗至少4个月。在烷化剂或干扰素治疗期间,大多数患者的疾病分期未发生变化。CLB未能提高NK活性,尽管它降低了淋巴细胞计数。虽然接受α-IFN治疗的患者淋巴细胞计数降低幅度未超过CLB治疗后的水平,但7例NK活性低的患者中有5例NK活性恢复到正常水平,2例NK活性正常的患者其NK活性保持在正常范围内。α-IFN治疗后,CD57+淋巴细胞(存在于NK细胞中的抗原)数量增加,而其余T淋巴细胞(CD2、CD4和CD8)及NK细胞(CD16和CD11b)亚群无变化。这些结果表明,α-IFN在体内可增强NK活性。

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