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Toll 样受体在宿主对重组减毒沙门氏菌载体疫苗表达的变异链球菌毒力抗原的反应中的作用。

Role of Toll-like receptors in host responses to a virulence antigen of Streptococcus mutans expressed by a recombinant, attenuated Salmonella vector vaccine.

机构信息

Department of Biomedical and Diagnostic Sciences, University of Detroit Mercy School of Dentistry, Detroit, MI 48208, United States.

出版信息

Vaccine. 2010 Jul 12;28(31):4928-36. doi: 10.1016/j.vaccine.2010.05.039.

Abstract

In the present study, we investigated the role of Toll-like receptors (TLRs) in host responses to the saliva-binding region (SBR) of Streptococcus mutans expressed by a recombinant, attenuated Salmonella vaccine. C57BL/6 wild type (wt), TLR2-/-, TLR4-/- and MyD88-/- mice were immunized by the intranasal route on days 0, 18 and boosted on day 98 with Salmonella typhimurium BRD 509 containing a plasmid encoding SBR. Serum and saliva samples were collected throughout the experiment and assessed for antibody activity by ELISA. Evidence is provided that the induction of a serum IgG2a (Th1-type) anti-SBR antibody response involved TLR2 signaling, whereas the anti-Salmonella response involved signaling through TLR4. The adaptor molecule MyD88 was not essential for the induction of a primary Th1-type response to SBR or Salmonella, but was necessary for a secondary response to SBR. Furthermore, the absence of TLR2, TLR4 or MyD88 resulted in enhanced Th2-type serum IgG1 anti-SBR and anti-Salmonella responses. Mucosal IgA responses to SBR were TLR2-, TLR4- and MyD88-dependent, while IgA responses to Salmonella were TLR4- and MyD88-dependent.

摘要

在本研究中,我们研究了 Toll 样受体 (TLRs) 在宿主对重组减毒沙门氏菌疫苗表达的变形链球菌唾液结合区 (SBR) 反应中的作用。C57BL/6 野生型 (wt)、TLR2-/-、TLR4-/-和 MyD88-/- 小鼠通过鼻腔途径在第 0、18 和 98 天进行免疫,用含有编码 SBR 的质粒的鼠伤寒沙门氏菌 BRD509 进行加强免疫。在整个实验过程中收集血清和唾液样本,并通过 ELISA 评估抗体活性。有证据表明,血清 IgG2a(Th1 型)抗 SBR 抗体反应的诱导涉及 TLR2 信号,而抗沙门氏菌反应则涉及 TLR4 信号。衔接分子 MyD88 对于 SBR 或沙门氏菌的初次 Th1 型反应的诱导不是必需的,但对于 SBR 的再次反应是必需的。此外,TLR2、TLR4 或 MyD88 的缺失导致 Th2 型血清 IgG1 抗 SBR 和抗沙门氏菌反应增强。SBR 的黏膜 IgA 反应依赖于 TLR2、TLR4 和 MyD88,而沙门氏菌的 IgA 反应依赖于 TLR4 和 MyD88。

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