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家族性地中海热中的免疫系统。

The immune system in familial Mediterranean fever.

作者信息

Melamed I, Shemer Y, Zakuth V, Tzehoval E, Pras M, Spirer Z

出版信息

Clin Exp Immunol. 1983 Sep;53(3):659-62.

Abstract

Familial Mediterranean fever (FMF) is a genetic disorder with an obscure aetiology. In attempts to investigate a possible immunoregulatory imbalance involved in this disease we tested 24 FMF patients for suppressor T cell activity and for chemotaxis of mononuclear cells. The suppressor T cell activity and chemotaxis were decreased in untreated FMF patients as compared to colchicine treated patients or normal controls. Amyloid FMF patients manifested significantly increased chemotactic activity, while the suppressor T cell activity was normal. This finding may extend our knowledge concerning the immune mechanism involved in FMF.

摘要

家族性地中海热(FMF)是一种病因不明的遗传性疾病。为了研究该疾病可能涉及的免疫调节失衡,我们对24例FMF患者进行了抑制性T细胞活性和单核细胞趋化性检测。与秋水仙碱治疗的患者或正常对照组相比,未经治疗的FMF患者的抑制性T细胞活性和趋化性降低。淀粉样变FMF患者的趋化活性显著增加,而抑制性T细胞活性正常。这一发现可能会扩展我们对FMF所涉及免疫机制的认识。

相似文献

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1
Immunoregulatory abnormalities in familial Mediterranean fever.家族性地中海热中的免疫调节异常。
Clin Immunol Immunopathol. 1981 Feb;18(2):261-7. doi: 10.1016/0090-1229(81)90032-5.
7
Letter: Colchicine in familial Mediterranean fever.信件:秋水仙碱治疗家族性地中海热。
N Engl J Med. 1976 Jan 15;294(3):170-1. doi: 10.1056/NEJM197601152940327.
8
Leukocyte function in familial Mediterranean fever.
Am J Hematol. 1976;1(3):307-11. doi: 10.1002/ajh.2830010304.
10
Monocyte function in familial Mediterranean fever.
Am J Med Sci. 1977 Nov-Dec;274(3):265-70. doi: 10.1097/00000441-197711000-00004.

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