Department of Hematology, Amsterdam UMC, Amsterdam, the Netherlands; Department of Experimental Immunology, Amsterdam Institute for Infection and Immunity (AII), Cancer Center Amsterdam, Amsterdam UMC, Amsterdam.
Adult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Department of Medicine, Weill Cornell Medical College, New York, NY.
Haematologica. 2021 Aug 1;106(8):2042-2053. doi: 10.3324/haematol.2020.270835.
Microbiota injury occurs in many patients undergoing allogeneic hematopoietic cell transplantation, likely as a consequence of conditioning regimens involving chemo- and radiotherapy, the widespread use of both prophylactic and therapeutic antibiotics, and profound dietary changes during the peri-transplant period. Peri-transplant dysbiosis is characterized by a decrease in bacterial diversity, loss of commensal bacteria and single-taxon domination (e.g., with Enterococcal strains). Clinically, deviation of the post-transplant microbiota from a normal, high-diversity, healthy state has been associated with increased risk of bacteremia, development of graft-versus-host disease and decreases in overall survival. A number of recent clinical trials have attempted to target the microbiota in allogeneic hematopoietic cell transplantation patients via dietary interventions, selection of therapeutic antibiotics, administration of pre- or pro-biotics, or by performing fecal microbiota transplantation. These strategies have yielded promising results but the mechanisms by which these interventions influence transplant-related complications remain largely unknown. In this review we summarize the current approaches to targeting the microbiota, discuss potential underlying mechanisms and highlight the key outstanding areas that require further investigation in order to advance microbiota- targeting therapies.
在许多接受异基因造血细胞移植的患者中会发生微生物组损伤,这可能是由于涉及化疗和放疗的预处理方案、广泛使用预防性和治疗性抗生素以及移植期间饮食的巨大变化所致。移植期间的微生态失调的特征是细菌多样性减少、共生菌丧失和单种优势(例如肠球菌株)。临床上,移植后微生物组偏离正常的高多样性健康状态与菌血症风险增加、移植物抗宿主病的发展以及总生存率降低有关。最近的一些临床试验试图通过饮食干预、选择治疗性抗生素、给予益生菌或粪便微生物移植来靶向异基因造血细胞移植患者的微生物组。这些策略取得了有希望的结果,但这些干预措施影响移植相关并发症的机制在很大程度上仍不清楚。在这篇综述中,我们总结了靶向微生物组的当前方法,讨论了潜在的潜在机制,并强调了需要进一步研究的关键未决领域,以推进靶向微生物组治疗。