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小鼠干扰素对淋巴细胞再循环的抑制作用:不同干扰素制剂及给药时间的影响

Inhibition of lymphocyte recirculation by murine interferon: effects of various interferon preparations and timing of administration.

作者信息

Mann E A, Markovic S N, Murasko D M

机构信息

Department of Microbiology and Immunology, Medical College of Pennsylvania, Philadelphia 19129.

出版信息

J Interferon Res. 1989 Feb;9(1):35-51. doi: 10.1089/jir.1989.9.35.

Abstract

The effects of highly purified and/or recombinant interferon (IFN)-alpha/beta, IFN-alpha, IFN-beta, IFN-gamma, and the IFN-inducer, poly(I):poly(C), on the circulation of peripheral blood leukocytes (PBL) and thoracic duct lymphocytes (TDL) of (BALB/cJ x C57Bl/6J)F1 mice were examined. Although all IFN classes could depress significantly the number of circulating PBL and TDL when given at sufficient doses, IFN-alpha appeared to be the most potent. Phenotypic analysis of lymphocytes in the blood and lymph during the decrease induced by IFN suggests that IFN-alpha/beta and IFN-alpha preferentially decrease the Lyt-2+, or suppressor/cytotoxic, subset. Timing of IFN administration was found to be an important factor. Repeated administration of IFN-alpha/beta once a day for 3 days produced continuous suppression of the number of circulating PBL. Administration of either IFN-alpha/beta or IFN-gamma in the evening resulted in a longer and more extensive inhibition of PBL circulation than when IFN was administered in the morning. Our results suggest that the leukopenia observed in many patients undergoing IFN therapy may, in part, be attributed to decreased lymphocyte recirculation, and that the timing of IFN administration may be important in maximizing its therapeutic index.

摘要

研究了高纯度和/或重组干扰素(IFN)-α/β、IFN-α、IFN-β、IFN-γ以及IFN诱导剂聚肌苷酸:聚胞苷酸[poly(I):poly(C)]对(BALB/cJ×C57Bl/6J)F1小鼠外周血白细胞(PBL)和胸导管淋巴细胞(TDL)循环的影响。尽管给予足够剂量时所有类型的干扰素均可显著降低循环中的PBL和TDL数量,但IFN-α似乎作用最强。对干扰素诱导数量减少期间血液和淋巴中的淋巴细胞进行表型分析表明,IFN-α/β和IFN-α优先减少Lyt-2+细胞亚群,即抑制性/细胞毒性亚群。发现干扰素给药时间是一个重要因素。每天重复给予IFN-α/β,连续3天可持续抑制循环中PBL的数量。晚上给予IFN-α/β或IFN-γ比早上给药导致对PBL循环的抑制作用更持久、更广泛。我们的结果表明,许多接受干扰素治疗的患者出现的白细胞减少可能部分归因于淋巴细胞再循环减少,并且干扰素给药时间对于最大化其治疗指数可能很重要。

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