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镰状细胞贫血患者血清对鼠伤寒沙门氏菌杀菌活性的缺乏。

Deficiency of serum bactericidal activity against Salmonella typhimurium in sickle cell anaemia.

作者信息

Hand W L, King N L

出版信息

Clin Exp Immunol. 1977 Nov;30(2):262-70.

Abstract

Systemic salmonellosis is a recognized complication of sickle cell anemia (SCA). In our initial study of SCA host defences against salmonella, we evaluated the bactericidal activity of serum against Salmonella typhimurium. When compared to controls, sera from eight out of nineteen SCA patients were deficient in bactericidal function. Levels of factor B, haemolytic complement and agglutinating antibody were similar in SCA and control sera. However, abnormalities that might theoretically account for the decreased antibacterial activity were observed in many SCA sera. These abnormal findings included: (a) defective function of the alternative complement pathway (decreased bacterial killing in the presence of Mg EGTA); (b) low serum C3 concentration; and (c) decreased total iron-binding capacity (TIBC), with a resultant increase in per cent saturation of iron-binding capacity. Of these deficiencies only the abnormal alternative pathway function was significantly associated with decreased serum bactericidal activity. A suggested function of serum bactericidal activity is prevention of bacteraemia by susceptible organisms. Thus diminished serum bactericidal capacity may increase the risk of Salmonella bacteraemia in some individuals with sickle cell disease.

摘要

全身性沙门氏菌病是镰状细胞贫血(SCA)一种公认的并发症。在我们最初关于SCA宿主对沙门氏菌防御机制的研究中,我们评估了血清对鼠伤寒沙门氏菌的杀菌活性。与对照组相比,19名SCA患者中有8名患者的血清杀菌功能存在缺陷。SCA患者血清和对照血清中的B因子、溶血补体和凝集抗体水平相似。然而,在许多SCA患者血清中观察到了一些理论上可能导致抗菌活性降低的异常情况。这些异常发现包括:(a)替代补体途径功能缺陷(在Mg EGTA存在的情况下细菌杀伤能力降低);(b)血清C3浓度低;(c)总铁结合能力(TIBC)降低,导致铁结合能力的饱和度百分比增加。在这些缺陷中,只有替代途径功能异常与血清杀菌活性降低显著相关。血清杀菌活性的一个推测功能是预防易感生物体引起的菌血症。因此,血清杀菌能力的降低可能会增加一些镰状细胞病患者发生沙门氏菌菌血症的风险。

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