Institute for Immunity, Transplantation, Infection, Stanford University School of Medicine, Stanford, CA 94305, United States of America.
Sean Parker Center for Allergy and Asthma Research, Stanford University School of Medicine, Stanford, CA 94305, United States of America.
Clin Immunol. 2020 Oct;219:108568. doi: 10.1016/j.clim.2020.108568. Epub 2020 Aug 9.
Oral immunotherapy (OIT) can successfully desensitize allergic individuals to offending foods such as peanut. Our recent clinical trial (NCT02103270) of peanut OIT allowed us to monitor peanut-specific CD4+ T cells, using MHC-peptide Dextramers, over the course of OIT. We used a single-cell targeted RNAseq assay to analyze these cells at 0, 12, 24, 52, and 104 weeks of OIT. We found a transient increase in TGFβ-producing cells at 52 weeks in those with successful desensitization, which lasted until 117 weeks. We also performed clustering and identified 5 major clusters of Dextramer+ cells, which we tracked over time. One of these clusters appeared to be anergic, while another was consistent with recently described TFH13 cells. The other 3 clusters appeared to be Th2 cells by their coordinated production of IL-4 and IL-13, but they varied in their expression of STAT signaling proteins and other markers. A cluster with high expression of STAT family members also showed a possible transient increase at week 24 in those with successful desensitization. Single cell TCRαβ repertoire sequences were too diverse to track clones over time. Together with increased TGFβ production, these changes may be mechanistic predictors of successful OIT that should be further investigated.
口服免疫疗法(OIT)可以成功地使过敏个体对花生等过敏原脱敏。我们最近的花生 OIT 临床试验(NCT02103270)使我们能够在 OIT 过程中使用 MHC-肽 Dextramers 监测花生特异性 CD4+T 细胞。我们使用单细胞靶向 RNAseq 分析在 OIT 的 0、12、24、52 和 104 周时这些细胞。我们发现,在成功脱敏的患者中,52 周时 TGFβ 产生细胞一过性增加,持续到 117 周。我们还进行了聚类分析,鉴定了 Dextramer+细胞的 5 个主要簇,并随时间进行跟踪。其中一个簇似乎无反应,另一个簇与最近描述的 TFH13 细胞一致。其他 3 个簇通过协调产生 IL-4 和 IL-13 似乎表现为 Th2 细胞,但它们在 STAT 信号蛋白和其他标记物的表达上存在差异。一个高表达 STAT 家族成员的簇在成功脱敏的患者中也可能在第 24 周短暂增加。单细胞 TCRαβ 库序列太过多样化,无法随时间跟踪克隆。与 TGFβ 产生增加一起,这些变化可能是 OIT 成功的机制预测因子,应进一步研究。