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针对肺炎链球菌完整菌 versus 肺炎球菌结合疫苗的体内 14 型荚膜多糖特异性 Ig 反应的差异独特型利用。

Differential idiotype utilization for the in vivo type 14 capsular polysaccharide-specific Ig responses to intact Streptococcus pneumoniae versus a pneumococcal conjugate vaccine.

机构信息

Department of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.

出版信息

J Immunol. 2012 Jul 15;189(2):575-86. doi: 10.4049/jimmunol.1200599. Epub 2012 Jun 15.

DOI:10.4049/jimmunol.1200599
PMID:22706079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3392520/
Abstract

Murine IgG responses specific for the capsular polysaccharide (pneumococcal capsular polysaccharide serotype 14; PPS14) of Streptococcus pneumoniae type 14 (Pn14), induced in response to intact Pn14 or a PPS14-protein conjugate, are both dependent on CD4(+) T cell help but appear to use marginal zone versus follicular B cells, respectively. In this study, we identify an idiotype (44.1-Id) that dominates the PPS14-specific IgG, but not IgM, responses to intact Pn14, isolated PPS14, and Group B Streptococcus (strain COH1-11) expressing capsular polysaccharide structurally identical to PPS14. The 44.1-Id, however, is not expressed in the repertoire of natural PPS14-specific Abs. In distinct contrast, PPS14-specific IgG responses to a soluble PPS14-protein conjugate exhibit minimal usage of the 44.1-Id, although significant 44.1-Id expression is elicited in response to conjugate attached to particles. The 44.1-Id elicited in response to intact Pn14 was expressed in similar proportions among all four IgG subclasses during both the primary and secondary responses. The 44.1-Id usage was linked to the Igh(a), but not Igh(b), allotype and was associated with induction of relatively high total PPS14-specific IgG responses. In contrast to PPS14-protein conjugate, avidity maturation of the 44.1-Id-dominant PPS14-specific IgG responses was limited, even during the highly boosted T cell-dependent PPS14-specific secondary responses to COH1-11. These results indicate that different antigenic forms of the same capsular polysaccharide can recruit distinct B cell clones expressing characteristic idiotypes under genetic control and suggest that the 44.1-Id is derived from marginal zone B cells.

摘要

针对肺炎链球菌 14 型(Pn14)的荚膜多糖(肺炎球菌荚膜多糖血清型 14;PPS14)的鼠 IgG 反应,无论是针对完整的 Pn14 还是 PPS14-蛋白缀合物诱导的反应,都依赖于 CD4(+)T 细胞的帮助,但似乎分别使用边缘区 B 细胞和滤泡 B 细胞。在这项研究中,我们鉴定了一种独特型(44.1-Id),它主导了针对完整 Pn14、分离的 PPS14 和表达与 PPS14 结构相同荚膜多糖的 B 组链球菌(COH1-11 株)的 PPS14 特异性 IgG,但不包括 IgM 反应。然而,44.1-Id 并不表达在天然 PPS14 特异性 Abs 的 repertoire 中。与此形成鲜明对比的是,针对可溶性 PPS14-蛋白缀合物的 PPS14 特异性 IgG 反应几乎没有使用 44.1-Id,尽管在缀合物附着于颗粒时会引起显著的 44.1-Id 表达。针对完整的 Pn14 诱导的 44.1-Id 在初次和再次应答期间,在所有四个 IgG 亚类中以相似的比例表达。44.1-Id 的使用与 Igh(a),而不是 Igh(b),同种型相关,并且与诱导相对较高的总 PPS14 特异性 IgG 反应相关。与 PPS14-蛋白缀合物相反,44.1-Id 主导的 PPS14 特异性 IgG 反应的亲和力成熟受到限制,即使在高度增强的 T 细胞依赖性 PPS14 特异性针对 COH1-11 的二次反应中也是如此。这些结果表明,同一荚膜多糖的不同抗原形式可以在遗传控制下招募表达特征性独特型的不同 B 细胞克隆,并表明 44.1-Id 源自边缘区 B 细胞。

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本文引用的文献

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Structurally identical capsular polysaccharide expressed by intact group B streptococcus versus Streptococcus pneumoniae elicits distinct murine polysaccharide-specific IgG responses in vivo.完整的 B 组链球菌与肺炎链球菌表达的结构相同的荚膜多糖在体内诱导出截然不同的小鼠多糖特异性 IgG 应答。
J Immunol. 2012 Jun 1;188(11):5238-46. doi: 10.4049/jimmunol.1200132. Epub 2012 Apr 20.
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Mechanisms underlying in vivo polysaccharide-specific immunoglobulin responses to intact extracellular bacteria.体内完整胞外菌多糖特异性免疫球蛋白应答的作用机制。
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Identification of Bcl-6-dependent follicular helper NKT cells that provide cognate help for B cell responses.鉴定依赖 Bcl-6 的滤泡辅助 NKT 细胞,为 B 细胞反应提供同源帮助。
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A mechanism for glycoconjugate vaccine activation of the adaptive immune system and its implications for vaccine design.糖缀合物疫苗激活适应性免疫系统的机制及其对疫苗设计的意义。
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What is the best way to use conjugate vaccines?应该如何使用结合疫苗?
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