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