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对b型流感嗜血杆菌荚膜多糖-破伤风类毒素结合物在患有IgG亚类缺陷和频繁感染的成年人中引发的抗体反应进行定性和定量分析。

Qualitative and quantitative analyses of the antibody response elicited by Haemophilus influenzae type b capsular polysaccharide-tetanus toxoid conjugates in adults with IgG subclass deficiencies and frequent infections.

作者信息

Avanzini M A, Björkander J, Söderström R, Söderström T, Schneerson R, Robbins J B, Hanson L A

机构信息

Department of Paediatrics, University of Pavia, Italy.

出版信息

Clin Exp Immunol. 1994 Apr;96(1):54-8. doi: 10.1111/j.1365-2249.1994.tb06229.x.

Abstract

Twenty-one IgG subclass-deficient adult patients with repeated infections of the respiratory tract, were immunized with Haemophilus influenzae type b capsular polysaccharide (HibCP) covalently bound to tetanus toxoid (TT). Specific immunoglobulin and IgG subclasses to HibCP and TT were quantified; the biological activities of HibCP antibodies were also investigated. Most patients showed an antibody response similar to that observed in healthy adults, and the bactericidal activity related to the post-immunization levels of HibCP antibodies. No relation was found between immunoglobulin isotype deficiency, the clinical symptoms and the IgG subclass responsiveness, and no relation was observed between HibCP and TT antibody responses. Our data indicate that some, but not all, patients with recurrent infections and IgG subclass deficiency have an abnormal serum antibody response to polysaccharide and protein epitopes of Hib-TT conjugate vaccine. Analysis of the antibody response after vaccination with HibCP-TT conjugate vaccine did not seem to predict the clinical course of such patients.

摘要

21例患有反复呼吸道感染的IgG亚类缺陷成年患者,用与破伤风类毒素(TT)共价结合的b型流感嗜血杆菌荚膜多糖(HibCP)进行免疫。对HibCP和TT的特异性免疫球蛋白及IgG亚类进行定量;还研究了HibCP抗体的生物学活性。大多数患者表现出与健康成年人相似的抗体反应,且杀菌活性与免疫后HibCP抗体水平相关。未发现免疫球蛋白同种型缺陷、临床症状与IgG亚类反应性之间存在关联,也未观察到HibCP与TT抗体反应之间存在关联。我们的数据表明,一些(但并非全部)患有反复感染和IgG亚类缺陷的患者对Hib-TT结合疫苗的多糖和蛋白质表位有异常的血清抗体反应。接种HibCP-TT结合疫苗后的抗体反应分析似乎无法预测此类患者的临床病程。

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Antibody response to Haemophilus influenzae type b capsular polysaccharide conjugated to tetanus toxoid in preterm infants.
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