Department of Pathogen Biology, National Vaccine Innovation Platform, Jiangsu Province Engineering Research Center of Antibody Drug, School of Basic Medical Sciences, Nanjing Medical University, Nanjing, China.
Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences/Key Laboratory of Bioactive Peptides of Yunnan Province, Kunming Institute of Zoology, China.
EBioMedicine. 2023 Sep;95:104751. doi: 10.1016/j.ebiom.2023.104751. Epub 2023 Aug 12.
Regulatory T cells (Tregs) can alleviate the development of autoimmune and inflammatory diseases, thereby proposing their role as a new therapeutic strategy. Parasitic helminths have co-evolved with hosts to generate immunological privilege and immune tolerance through inducing Tregs. Thus, constructing a "Tregs-induction"-based discovery pipeline from parasitic helminth is a promising strategy to control autoimmune and inflammatory diseases.
The gel filtration chromatography and reverse-phase high-performance liquid chromatography (RP-HPLC) were used to isolate immunomodulatory components from the egg extracts of Schistosoma japonicum. The extracted peptides were evaluated for their effects on Tregs suppressive functions using flow cytometry, ELISA and T cell suppression assay. Finally, we carried out colitis and psoriasis models to evaluate the function of Tregs induced by helminth-derived peptide in vivo.
Here, based on target-driven discovery strategy, we successfully identified a small 3 kDa peptide (SjDX5-53) from egg extracts of schistosome, which promoted both human and murine Tregs production. SjDX5-53 presented immunosuppressive function by arresting dendritic cells (DCs) at an immature state and augmenting the proportion and suppressive capacity of Tregs. In mouse models, SjDX5-53 protected mice against autoimmune-related colitis and psoriasis through inducing Tregs and inhibiting inflammatory T-helper (Th) 1 and Th17 responses.
SjDX5-53 exhibited the promising therapeutic effects in alleviating the phenotype of immune-related colitis and psoriasis. This study displayed a screening and validation pipeline of the inducer of Tregs from helminth eggs, highlighting the discovery of new biologics inspired by co-evolution of hosts and their parasites.
This study was supported by the Natural Science Foundation of China (82272368) and Natural Science Foundation of Jiangsu Province (BK20211586).
调节性 T 细胞(Tregs)可减轻自身免疫和炎症性疾病的发展,因此提出了将其作为一种新的治疗策略的作用。寄生虫吸虫通过诱导 Tregs 与宿主共同进化以产生免疫特权和免疫耐受。因此,从寄生虫吸虫中构建基于“Tregs 诱导”的发现途径是控制自身免疫和炎症性疾病的一种很有前途的策略。
使用凝胶过滤色谱和反相高效液相色谱(RP-HPLC)从日本血吸虫卵提取物中分离免疫调节成分。使用流式细胞术、ELISA 和 T 细胞抑制试验评估提取的肽对 Tregs 抑制功能的影响。最后,我们进行了结肠炎和银屑病模型,以评估寄生虫来源肽诱导的 Tregs 在体内的功能。
在这里,基于靶向发现策略,我们成功地从血吸虫卵提取物中鉴定出一种 3kDa 的小肽(SjDX5-53),它促进了人和鼠 Tregs 的产生。SjDX5-53 通过将树突状细胞(DC)阻滞在未成熟状态并增加 Tregs 的比例和抑制能力来发挥免疫抑制作用。在小鼠模型中,SjDX5-53 通过诱导 Tregs 并抑制炎症性辅助性 T 细胞(Th)1 和 Th17 反应,保护小鼠免受自身免疫相关结肠炎和银屑病的侵害。
SjDX5-53 在缓解与免疫相关的结肠炎和银屑病表型方面表现出有希望的治疗效果。本研究展示了一种从寄生虫卵中筛选和验证 Tregs 诱导物的筛选和验证途径,强调了从宿主及其寄生虫的共同进化中发现新生物制剂的研究。
本研究得到了中国自然科学基金(82272368)和江苏省自然科学基金(BK20211586)的支持。