医学
CD8型
造血干细胞移植
免疫学
移植物抗宿主病
移植
调节性T细胞
干细胞
T细胞
免疫系统
内科学
生物
白细胞介素2受体
遗传学
作者
Jennifer Whangbo,Sarah Nikiforow,Haesook T. Kim,Jonathan L. Wahl,Carol Reynolds,Sharmila Chamling,Soomin Kim,Andrew Thomas Burden,Ana Cristina Alho,João F. Lacerda,Edwin P. Alyea,Corey Cutler,Vincent T. Ho,Joseph H. Antin,Robert J. Soiffer,Jérôme Ritz,John Koreth
出处
期刊:Blood Advances
[Elsevier BV]
日期:2022-11-08
卷期号:6 (21): 5786-5796
被引量:16
标识
DOI:10.1182/bloodadvances.2021006625
摘要
Chronic graft-versus-host disease (cGVHD) remains a frequent cause of nonrelapse morbidity and mortality after allogeneic hematopoietic stem cell transplantation. Despite recent advances, options for steroid-refractory (SR) cGVHD are limited. In previous trials of low-dose interleukin-2 (LD IL-2), the immunomodulatory properties of regulatory T cells (Tregs) have been harnessed to treat SR-cGVHD safely and effectively. In the present study, we combined a single infusion of Treg-enriched lymphocytes (Treg DLI) from the original stem cell donor with in vivo Treg expansion using LD IL-2 (1 × 106 IU/m2 per day for 8 weeks) in 25 adult patients with SR-cGVHD. Treg were not expanded ex vivo. Treg DLI was initiated at 0.1 × 106 cells per kg patient and escalated to a maximum dose of 1 × 106 cells per kg. Treg DLI plus LD IL-2 was well tolerated and led to partial responses (PR) in 5 of 25 patients (20%) after 8 weeks of therapy. Ten additional patients (40%) had stable disease with minor responses not meeting PR criteria. Patients at all dose levels had similar Treg expansion without significant changes in CD4+ conventional T cells or CD8+ T cells. High-throughput sequencing of the T-cell receptor β locus showed selective improvement of Treg diversity. A subset of DLI-derived Treg clones showed preferential expansion at week 8 and long-term persistence 1-year postinfusion. We demonstrate for the first time that infusion of polyclonal healthy donor Tregs followed by expansion with LD IL-2 is safe in patients with SR-cGVHD, thus establishing a foundation for future adoptive Treg therapies in the posttransplant setting. This trial was registered at www.clinicaltrials.gov as #NCT01937468.
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