Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI 48201, USA.
CNS Neurosci Ther. 2013 Jul;19(7):503-10. doi: 10.1111/cns.12087. Epub 2013 Mar 22.
Administration of antigens into the anterior chamber (AC) of the eye induces a form of antigen-specific immune tolerance termed anterior chamber-associated immune deviation (ACAID). This immune tolerance effectively impairs host delayed-type hypersensitivity (DTH) responses. We hypothesized that ACAID could be generated in BALB/c mice following AC inoculation of the encephalitogenic antigens myelin oligodendrocyte glycoprotein (MOG) and myelin basic protein (MBP).
We used DTH assays and local adoptive transfer (LAT) assays to test whether MOG/MBP-induced ACAID following their administration into the AC, whether they elicited this immune tolerance via CD8(+) T cells, and whether their AC coadministration (MOG/MBP) induced specific immune tolerance to one or both antigens.
We showed that MOG/MBP-induced AC-mediated specific immune tolerance, as evident from impaired DTH responses. This antigen-driven DTH suppression was solely mediated via splenic CD8(+) T cells as confirmed by LAT assays. Finally, a single AC injection with both antigens was sufficient to induce specific immune tolerance to these antigens, as evident from DTH and LAT assays.
ACAID T-cell regulation could be used as a therapeutic tool in the treatment of complicated autoimmune diseases that involve multiple antigens such as multiple sclerosis.
将抗原注入眼睛的前房(AC)会引起一种称为前房相关免疫偏离(ACAID)的抗原特异性免疫耐受形式。这种免疫耐受有效地损害了宿主迟发型超敏反应(DTH)反应。我们假设,在 BALB/c 小鼠的前房接种致脑炎抗原髓鞘少突胶质细胞糖蛋白(MOG)和髓鞘碱性蛋白(MBP)后,可产生 ACAID。
我们使用 DTH 测定和局部过继转移(LAT)测定来测试 MOG/MBP 在前房给药后是否会引起 ACAID,它们是否通过 CD8(+)T 细胞引起这种免疫耐受,以及它们在前房共同给药(MOG/MBP)是否会引起对一种或两种抗原的特异性免疫耐受。
我们表明,MOG/MBP 诱导的 AC 介导的特异性免疫耐受,如 DTH 反应受损所证明。这种抗原驱动的 DTH 抑制仅通过脾 CD8(+)T 细胞介导,如 LAT 测定所证实。最后,单次 AC 注射两种抗原足以诱导对这些抗原的特异性免疫耐受,如 DTH 和 LAT 测定所示。
ACAID T 细胞调节可作为治疗涉及多种抗原(如多发性硬化症)的复杂自身免疫性疾病的治疗工具。