HLA-DRB1*04 阳性受试者的总 IgA 和 IgA 对抗原 I/II 表位的反应性。

V Wallace McCarlie, James K Hartsfield, Janice S Blum, Carlos González-Cabezas, Judith R Chin, George J Eckert, Lorri A Morford, Mark D Pescovitz, Henry Rodriguez, Margherita Fontana, Richard L Gregory
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引用次数: 0

摘要

细菌粘附在获得性牙本质上对龋齿(龋齿)很重要,这种粘附是由受体粘附素介导的,如唾液凝集素与变异链球菌抗原 I/II(I/II)的结合。我们选择了十个 I/II 表位来确定它们与人类唾液 IgA 的反应性。以前的研究表明,一个特定的 HLA 生物标记群(HLA-DRB1*04)可能会对 I/II 的免疫反应产生不同的影响。然而,HLA-DRB1*04阳性受试者对所选表位的分泌型IgA(SIgA)反应与对照组相比是否存在差异,或与总IgA(TIgA)等其他龋病相关因素相比是否存在差异,目前尚不清楚。共有 32 名受试者根据 HLA 类型、性别、种族和年龄进行了配对。进行了 HLA 基因分型、口腔细菌、免疫球蛋白和抗体分析。观察发现,HLA-DRB1*04 阳性受试者的 TIgA 天然免疫库存在很大差异,具体来说,与对照组相比减少了 27.6%。与研究的所有其他表位相比,HLA-DRB1*04 阳性受试者对 I/II 表位 834-853 的反应性也有所降低。HLA-DRB1*04 阳性受试者对 834-853 的特异性 SIgA 活性/TIgA 较低,对 834-853/whole cell S. mutans UA159 的特异性反应也较低。此外,HLA-DRB1*04 阳性受试者对 I/II 的整体反应较低。观察到的 TIgA 和 834-853 反应模式在多种测量中的巨大差异表明,HLA-DRB1*04 与龋齿之间可能存在重要联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Total IgA and IgA reactivity to antigen I/II epitopes in HLA-DRB1*04 positive subjects.

Total IgA and IgA reactivity to antigen I/II epitopes in HLA-DRB1*04 positive subjects.

Total IgA and IgA reactivity to antigen I/II epitopes in HLA-DRB1*04 positive subjects.

Total IgA and IgA reactivity to antigen I/II epitopes in HLA-DRB1*04 positive subjects.

Bacterial adherence to the acquired dental pellicle, important in dental caries (caries), is mediated by receptor-adhesins such as salivary agglutinin binding to Streptococcus mutans antigen I/II (I/II). Ten selected I/II epitopes were chosen to determine their reactivity to human salivary IgA. Previous studies suggested that a specific HLA biomarker group (HLA-DRB1*04) may have differential influence of immune responses to I/II. However, it was not known whether secretory IgA (SIgA) responses to the selected epitopes from HLA-DRB1*04 positive subjects were different compared to controls, or across other caries-related factors such as total IgA (TIgA). Thirty-two total subjects were matched according to HLA type, gender, ethnicity and age. HLA genotyping, oral bacterial, immunoglobulin and antibody analyses were performed. A large observed difference emerged with regard to the natural immune reservoir of TIgA in HLA-DRB1*04 positive subjects, specifically, a 27.6% reduction compared to controls. In contrast to all other epitopes studied, HLA-DRB1*04 positive subjects also exhibited reduced reactivity to I/II epitope 834-853. HLA-DRB1*04 positive subjects exhibited lower specific SIgA activity/TIgA to 834-853 and also a lower specific reactivity to 834-853/whole cell S. mutans UA159. Furthermore, HLA-DRB1*04 positive subjects exhibited lower responses to I/II in its entirety. The large observed difference in TIgA and the 834-853 reactivity pattern across multiple measures suggest potentially important connections pertaining to the link between HLA-DRB1*04 and caries.

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