Reparative immunological consequences of stem cell transplantation as a cellular therapy for refractory Crohn's disease.

• Tác giả: Judy Cho, Louis Cohen, Jean-Frederic Colombel, Andrew Davis, Aaron Etra, James L M Ferrara, Elbek Fozilov, Daniela Guisado, Ronald Hoffman, John E Levine, Chuang Ling-Shiang, Bridget K Marcellino, Ksenija Sabic, Christoph Schaniel, Shishir Singh, Sayali Talware, Christopher Tastad, Xiaoli Wang
• Ngôn ngữ: eng
• Ký hiệu phân loại: 666.72 Refractory materials
• Thông tin xuất bản: England : Gut , 2025
• Bộ sưu tập: NCBI
• ID: 183797

Tóm tắt

BACKGROUND: Treatment strategies for Crohn's disease (CD) suppress diverse inflammatory pathways but many patients remain refractory to treatment. Autologous haematopoietic stem cell transplantation (SCT) is an emerging therapy for medically refractory CD though the mechanisms through which it circumvents refractory pathophysiology are unknown. OBJECTIVE: The objective of this study is to understand how the immune system reconstitutes post-SCT and whether SCT may function as a cellular therapy restoring appropriately responsive immune cell populations from haematopoietic stem cells (HSCs). DESIGN: Adults with CD with active clinical and endoscopic disease who failed available medical therapies were enrolled in a phase II study of SCT for refractory CD (n=19). Blood and intestinal samples were collected longitudinally and analysed using CyTOF and scRNA-seq. Stem cell autografts were functionally assayed in mouse xenograft models. RESULTS: scRNA-seq and CyTOF analyses reveal that SCT predominantly affected the intestinal myeloid lineage with loss of inflammatory populations and return of macrophages capable of supporting mucosal healing. Xenograft models using patient HSCs suggested that HSCs support the early reconstitution of the myeloid lineage and reveal an impairment of short and long-term HSC engraftment that may determine SCT outcomes. CONCLUSIONS: This study suggests SCT functions as a myeloid-directed cellular therapy reinforcing the critical role of macrophages in refractory CD pathophysiology and as a target for cellular therapies. Furthermore, we report an unrecognised functional heterogeneity among HSC subpopulations in CD that may be relevant to our understanding of CD treatment and pathophysiology.