首页> 外文期刊>Microbial Pathogenesis >Binding of Porphyromonas gingivalis gingipains to human CD4(+) T cells preferentially down-regulates surface CD2 and CD4 with little affect on co-stimulatory molecule expression
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Binding of Porphyromonas gingivalis gingipains to human CD4(+) T cells preferentially down-regulates surface CD2 and CD4 with little affect on co-stimulatory molecule expression

机译:牙龈卟啉单胞菌与人CD4(+)T细胞的结合优先下调表面CD2和CD4,对共刺激分子表达影响很小

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The role of Porphyromonas gingivalis cysteine proteinases (gingipains) in the evasion of host cell-mediated immunity has not been fully determined. In this study, modulation by gingipains of accessory and co-stimulatory molecule expression on human CD4(+) T cells was evaluated. Arg-gingipain rather than Lys-gingipain binds to resting CD4(+) T cells in the presence of serum. The constitutive expression of CD28 on T cells was slightly up-regulated following challenge with gingipains, whereas CD45 and CD3 were not affected. Binding of anti-CD2 and anti-CD4 monoclonal antibodies (mAbs) was reduced after challenge of T cells with gingipains, but restored to 50 and 100%, respectively, of control levels, after 48h of incubation in medium depleted of gingipains. The induced expression, by anti-CD3 mAb, of CTLA-4, CD25, and CD40 ligand (CD40L) was decreased following incubation of T cells with gingipains which also led to decreased response to anti-CD3 and anti-CD28 mAbs as shown by reduction of interleukin-2 (IL-2) production. Cumulatively, these results indicate that activated gingipains attach to T cells and preferentially cleave CD2 and CD4 molecules, with potential to impair T cell responses at periodontal sites.
机译:牙龈卟啉单胞菌半胱氨酸蛋白酶(gingipains)在逃避宿主细胞介导的免疫中的作用尚未完全确定。在这项研究中,评估了人牙龈CD4(+)T细胞上辅助和共刺激分子表达的姜黄素的调节作用。在存在血清的情况下,Arg-gingipain而非Lys-gingipain与静止的CD4(+)T细胞结合。姜黄素激发后,T细胞上CD28的组成型表达略有上调,而CD45和CD3则不受影响。在用姜黄素攻击T细胞后,抗CD2和抗CD4单克隆抗体(mAbs)的结合降低,但在耗尽了姜黄素的培养基中孵育48小时后,分别恢复至对照水平的50%和100%。 T细胞与姜黄素孵育后,抗CD3 mAb诱导的CTLA-4,CD25和CD40配体(CD40L)的表达降低,这也导致对抗CD3和抗CD28 mAb的反应降低,如下所示:减少白介素2(IL-2)的产生。累积地,这些结果表明活化的齿龈蛋白酶附着于T细胞并优先裂解CD2和CD4分子,从而有可能损害牙周部位的T细胞反应。

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