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本文引用的文献

1
An intramolecular interaction involving the N terminus of a streptococcal adhesin affects its conformation and adhesive function.一种涉及链球菌黏附素 N 端的分子内相互作用会影响其构象和黏附功能。
J Biol Chem. 2013 May 10;288(19):13762-74. doi: 10.1074/jbc.M113.459974. Epub 2013 Mar 28.
2
The dental plaque microbiome in health and disease.口腔菌斑微生物组与健康和疾病。
PLoS One. 2013;8(3):e58487. doi: 10.1371/journal.pone.0058487. Epub 2013 Mar 8.
3
Dental caries from a molecular microbiological perspective.从分子微生物学角度看龋齿
Caries Res. 2013;47(2):89-102. doi: 10.1159/000345367. Epub 2012 Nov 30.
4
Beyond Streptococcus mutans: dental caries onset linked to multiple species by 16S rRNA community analysis.超越变异链球菌:通过 16S rRNA 群落分析发现,多种细菌与龋齿的发生有关。
PLoS One. 2012;7(10):e47722. doi: 10.1371/journal.pone.0047722. Epub 2012 Oct 16.
5
Host and bacterial phenotype variation in adhesion of Streptococcus mutans to matched human hosts.变异链球菌在黏附于匹配的人类宿主时的宿主和细菌表型变化。
Infect Immun. 2012 Nov;80(11):3869-79. doi: 10.1128/IAI.00435-12. Epub 2012 Aug 27.
6
Targeting a Neutralizing Epitope of HIV Envelope Gp120 by Immune Complex Vaccine.通过免疫复合物疫苗靶向HIV包膜糖蛋白120的一个中和表位
J AIDS Clin Res. 2012 Mar 9;S8(2). doi: 10.4172/2155-6113.S8-002.
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Antibody-induced conformational changes in herpes simplex virus glycoprotein gD reveal new targets for virus neutralization.抗体诱导单纯疱疹病毒糖蛋白 gD 的构象变化揭示了新的病毒中和靶标。
J Virol. 2012 Feb;86(3):1563-76. doi: 10.1128/JVI.06480-11. Epub 2011 Nov 30.
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Maturation-induced cloaking of neutralization epitopes on HIV-1 particles.HIV-1 粒子上中和表位的成熟诱导伪装。
PLoS Pathog. 2011 Sep;7(9):e1002234. doi: 10.1371/journal.ppat.1002234. Epub 2011 Sep 8.
9
A therapeutic anti-Streptococcus mutans monoclonal antibody used in human passive protection trials influences the adaptive immune response.在人体被动保护试验中使用的一种治疗性抗变异链球菌单克隆抗体影响适应性免疫反应。
Vaccine. 2011 Aug 26;29(37):6292-300. doi: 10.1016/j.vaccine.2011.06.027. Epub 2011 Jun 23.
10
Conformational alterations in the CD4 binding cavity of HIV-1 gp120 influencing gp120-CD4 interactions and fusogenicity of HIV-1 envelopes derived from brain and other tissues.HIV-1 gp120 中 CD4 结合腔的构象改变影响源自大脑和其他组织的 HIV-1 包膜的 gp120-CD4 相互作用和融合性。
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变形链球菌 AgI/II 免疫优势的改变:免疫调节抗体的启示。

Alterations in immunodominance of Streptococcus mutans AgI/II: lessons learned from immunomodulatory antibodies.

机构信息

Department of Oral Biology, University of Florida College of Dentistry, Gainesville, FL 32610, United States.

Department of Oral Biology, University of Florida College of Dentistry, Gainesville, FL 32610, United States.

出版信息

Vaccine. 2014 Jan 9;32(3):375-82. doi: 10.1016/j.vaccine.2013.11.023. Epub 2013 Nov 16.

DOI:10.1016/j.vaccine.2013.11.023
PMID:24252705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3901311/
Abstract

Streptococcus mutans antigen I/II (AgI/II) has been widely studied as a candidate vaccine antigen against human dental caries. In this report we follow up on prior studies that indicated that anti-AgI/II immunomodulatory monoclonal antibodies (MAbs) exerted their effects by destabilizing the native protein structure and exposing cryptic epitopes. We show here that similar results can be obtained by immunizing mice with truncated polypeptides out of the context of an intra-molecular interaction that occurs within the full-length molecule and that appears to dampen the functional response against at least two important target epitopes. Putative T cell epitopes that influenced antibody specificity were identified immediately upstream of the alanine-rich repeat domain. Adherence inhibiting antibodies could be induced against two discrete domains of the protein, one corresponding to the central portion of the molecule and the other corresponding to the C-terminus.

摘要

变形链球菌抗原 I/II(AgI/II)已被广泛研究作为针对人类龋齿的候选疫苗抗原。在本报告中,我们跟进了先前的研究,这些研究表明抗-AgI/II 免疫调节单克隆抗体(MAb)通过破坏天然蛋白质结构并暴露隐藏表位来发挥作用。我们在这里表明,通过用截断的多肽免疫小鼠,可以获得类似的结果,这些多肽在分子内相互作用的背景之外,这种相互作用似乎抑制了针对至少两个重要靶表位的功能反应。影响抗体特异性的潜在 T 细胞表位位于富含丙氨酸的重复结构域的上游。可以针对蛋白质的两个离散结构域诱导粘附抑制抗体,一个对应于分子的中心部分,另一个对应于 C 末端。