镰状细胞病中干扰素的产生

Lymphokine research Pub Date : 1990-01-01
S C Taylor, S J Shacks, S M Villicana, J Olivares, G A Dinkins
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引用次数: 0

摘要

镰状细胞病(SCD)中细胞因子产生的数据有限。在这项研究中,我们测量了62例SCD稳定状态患者和21例SCD危重状态患者的α (Poly - ic诱导)和γ (pha诱导)干扰素(IFN)水平。比较的正常对照(30名健康者和14名感染者)以类似方式进行评估。与正常健康对照组(65 +/- 14 U/ml)相比,稳定状态(35 +/- 6 U/ml)和危重状态(24 +/- 11 U/ml)两组的γ IFN产量均显著减少,P < 0.005。两组SCD感染均低于正常组(56 +/- 23 U/ml), P < 0.005。更仔细地分析个体滴度,与未感染的正常人(范围27-2187 U/ml)相比,稳定状态下有15/62(24%)、感染的SCD患者中有11/21(52%)和感染的正常人中有2/14(14%)显示γ IFN受损。SCD组α - IFN的产生;稳定状态(512 +/- 113 U/ml)和感染的SCD危重(559 +/- 110 U/ml)几乎等同于正常(524 +/- 170 U/ml)和感染的正常(509 +/- 116 U/ml)。与γ IFN相比,个体滴度分析也显示无显著差异。这些结果表明,在稳定状态和与危重相关的感染状态下,有相当比例的SCD患者γ - IFN产生受损。鉴于γ IFN已知的免疫调节功能,这种明显的缺陷可能是解释SCD感染频率和严重程度增加的另一个因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interferon production in sickle cell disease.

There is limited data on cytokine production in sickle cell disease (SCD). In this study, both alpha (Poly IC-induced) and gamma (PHA-induced) interferon (IFN) were measured in 62 SCD steady state patients, and 21 in the crisis state associated with infections. Comparable normal controls (30 healthy and 14 with infections) were assessed in a similar manner. Gamma IFN production in both SCD groups, steady state (35 +/- 6 U/ml) and crisis state (24 +/- 11 U/ml) was significantly diminished when compared to the normal healthy controls (65 +/- 14 U/ml) with P less than .005. Both SCD groups were also less than normals with infections (56 +/- 23 U/ml) with P less than .005. On closer analysis of individual titers, 15/62 (24%) in the steady state, 11/21 (52%) of SCD patients with infection and 2/14 (14%) of normals with infection, showed impaired gamma IFN when compared to normals without infection (range 27-2187 U/ml). Alpha IFN production in the SCD groups; steady state (512 +/- 113 U/ml) and SCD crisis with infection (559 +/- 110 U/ml) was virtually equivalent to normals (524 +/- 170 U/ml) and normals with infection (509 +/- 116 U/ml). Analysis of individual titers, in contrast to gamma IFN, also showed no significant differences. These results indicate that a significant percentage of SCD patients in both the steady state and infectious state associated with crisis, have impaired gamma IFN production. In view of the known immunomodulatory functions of gamma IFN, this apparent defect may be another factor to explain the increased frequency and severity of infections in SCD.

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