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在近期接种了寡糖-蛋白结合物的个体的人外周血淋巴细胞中体外诱导b型流感嗜血杆菌多糖特异性抗体反应

In vitro induction of a Haemophilus influenzae type b polysaccharide-specific antibody response in human peripheral blood lymphocytes of individuals recently vaccinated with an oligosaccharide-protein conjugate.

作者信息

Peeters C C, Tenbergen-Meekes A M, Heijnen C J, Poolman J T, Zegers B J, Rijkers G T

机构信息

Department of Immunology, University Hospital for Children and Youth het Wilhelmina Kinderziekenhuis, Utrecht, The Netherlands.

出版信息

J Immunol. 1991 Dec 15;147(12):4192-9.

PMID:1753096
Abstract

In this paper an in vitro culture system for the induction of an antibody response to the Haemophilus influenzae type b polysaccharide (PRP) is described. Anti-PRP IgM and IgG antibody-secreting cells (ASC) and anti-diphtheria toxoid (DT) IgG ASC were detected in cultures of blood B and T cells derived from donors 4 to 6 wk after immunization with Haemophilus influenzae type b oligosaccharide-mutant diphtheria toxin (CRM197) conjugate (HbOC) and required in vitro restimulation with HbOC. When lymphocytes from HbOC-vaccinated donors were stimulated with PRP, anti-PRP IgM and IgG ASC could be detected in 50% offGe cases. Lymphocytes from PRP-vaccinated donors or non-vaccinated donors consistently failed to generate anti-PRP antibodies after in vitro stimulation with HbOC. Optimal in vitro responses were observed at concentrations of 0.06 to 0.6 micrograms/ml of Ag. At higher doses of Ag (6 micrograms/ml) anti-PRP and anti-DT antibody responses were suppressed. The in vitro generation of anti-PRP and anti-DT ASC, as detected by a spot-forming cell assay was shown to be T cell dependent, Ag dependent, and Ag specific. This culture system provides a model for the study of human B cell activation and immunoregulation by polysaccharide-protein conjugates and polysaccharides.

摘要

本文描述了一种体外培养系统,用于诱导对b型流感嗜血杆菌多糖(PRP)的抗体反应。在用b型流感嗜血杆菌寡糖-突变型白喉毒素(CRM197)结合物(HbOC)免疫4至6周后,从供体获得的血液B细胞和T细胞培养物中检测到抗PRP IgM和IgG抗体分泌细胞(ASC)以及抗白喉类毒素(DT)IgG ASC,并且需要用HbOC进行体外再刺激。当用PRP刺激来自接种HbOC的供体的淋巴细胞时,在50%的病例中可检测到抗PRP IgM和IgG ASC。在用HbOC进行体外刺激后,来自接种PRP的供体或未接种的供体的淋巴细胞始终未能产生抗PRP抗体。在抗原浓度为0.06至0.6微克/毫升时观察到最佳的体外反应。在较高剂量的抗原(6微克/毫升)下,抗PRP和抗DT抗体反应受到抑制。通过斑点形成细胞试验检测到的抗PRP和抗DT ASC的体外产生显示为T细胞依赖性、抗原依赖性和抗原特异性。该培养系统为研究多糖-蛋白质结合物和多糖对人B细胞活化和免疫调节提供了一个模型。

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