Zhu Qiurong, Shayan Maryam, Huckfeldt Rachel M, Chen Yihe
Schepens Eye Research Institute of Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts, United States.
Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts, United States.
Invest Ophthalmol Vis Sci. 2025 May 1;66(5):9. doi: 10.1167/iovs.66.5.9.
We have previously demonstrated the pathogenic function of memory CD4+ T cells, which express IL-7 receptor (IL-7R) and IL-15R, in experimental chronic autoimmune uveitis (CAU). Here, we aimed to compare the therapeutic efficacy of blocking IL-7 or IL-15 in CAU.
C57BL/6J mice were induced for CAU, then intraperitoneally injected with an anti-IL-7 antibody (Ab), an anti-IL-15 Ab, or an IgG control for 2 weeks. Disease was evaluated by weekly fundoscopy, optical coherence tomography (OCT), and full-field electroretinography for four weeks from the initiation of treatment. At week 4, retina and cervical lymph nodes (CLN) were collected for flow cytometry analysis of T-cell response.
The anti-IL-7 Ab led to progressively reduced retinal infiltration and structural damage, with rapid recovery of retinal function. The anti-IL-15 Ab resulted in moderately reduced retinal infiltration and structural damage, along with a delayed, partial functional improvement. Compared to the control group, the anti-IL-7 Ab group exhibited significantly reduced disease scores from baseline on fundoscopy and OCT at week 4, and substantially improved dark-adapted (DA) a-wave and light-adapted b-wave responses at week 2; although the anti-IL-15 Ab group showed significantly improved disease from baseline only on OCT and increased DA b-waves at week 4. Both treatments effectively depleted the retinal infiltrating T cells and reduced memory Th17 cells in the CLN.
Our proof-of-concept study demonstrates that blocking IL-7 or IL-15 leads to specific depletion of the uveitogenic memory CD4+ T cells and disruption of disease chronicity in uveitis.
我们之前已经证明了表达白细胞介素-7受体(IL-7R)和IL-15R的记忆性CD4+ T细胞在实验性慢性自身免疫性葡萄膜炎(CAU)中的致病作用。在此,我们旨在比较阻断IL-7或IL-15在CAU中的治疗效果。
将C57BL/6J小鼠诱导为CAU,然后腹腔注射抗IL-7抗体(Ab)、抗IL-15 Ab或IgG对照,持续2周。从治疗开始后的四周内,通过每周一次的眼底镜检查、光学相干断层扫描(OCT)和全视野视网膜电图评估疾病情况。在第4周,收集视网膜和颈部淋巴结(CLN)用于T细胞反应的流式细胞术分析。
抗IL-7 Ab导致视网膜浸润和结构损伤逐渐减少,视网膜功能迅速恢复。抗IL-15 Ab导致视网膜浸润和结构损伤中度减少,同时功能改善延迟且部分改善。与对照组相比,抗IL-7 Ab组在第4周的眼底镜检查和OCT中疾病评分从基线显著降低,在第2周暗适应(DA)a波和明适应b波反应显著改善;尽管抗IL-15 Ab组仅在OCT上显示疾病从基线显著改善,且在第4周DA b波增加。两种治疗均有效耗尽视网膜浸润性T细胞并减少CLN中的记忆性Th17细胞。
我们的概念验证研究表明,阻断IL-7或IL-15可导致致葡萄膜炎的记忆性CD4+ T细胞特异性耗竭,并破坏葡萄膜炎的疾病慢性化。