Section of Hematology and Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA.
Program in Immunology, Graduate School of Biomedical Sciences, Baylor College of Medicine, Houston, TX 77030, USA.
Cells. 2021 Jan 30;10(2):277. doi: 10.3390/cells10020277.
Bone marrow suppression, including neutropenia, is a major adverse effect of prolonged antibiotic use that impairs the clinical care and outcomes of patients with serious infections. The mechanisms underlying antibiotic-mediated bone marrow suppression remain poorly understood, with initial evidence indicating that depletion of the intestinal microbiota is an important factor. Based on our earlier studies of blood and bone marrow changes in a mouse model of prolonged antibiotic administration, we studied whether changes in megakaryocytes or regulatory T cells (Tregs), two cell types that are critical in the maintenance of hematopoietic stem cells, contribute to antibiotic-mediated bone marrow suppression. Despite increased platelet numbers, megakaryocytes were unchanged in the bone marrow of antibiotic-treated mice; however, Tregs were found to be significantly depleted. Exogenous addition of Tregs was insufficient to rescue the function of bone marrow from antibiotic-treated mice in both colony formation and transplantation assays. These findings indicate that the intestinal microbiota support normal Treg development to protect healthy hematopoiesis, but that the restoration of Tregs alone is insufficient to restore normal bone marrow function.
骨髓抑制,包括中性粒细胞减少,是抗生素长期使用的主要不良反应,会损害严重感染患者的临床治疗和预后。抗生素介导的骨髓抑制的机制仍知之甚少,最初的证据表明,肠道微生物群的耗竭是一个重要因素。基于我们之前在抗生素长期给药的小鼠模型中对血液和骨髓变化的研究,我们研究了巨核细胞或调节性 T 细胞(Tregs)的变化是否有助于抗生素介导的骨髓抑制,这两种细胞类型对于维持造血干细胞至关重要。尽管血小板数量增加,但抗生素治疗小鼠的骨髓中巨核细胞没有变化;然而,发现 Tregs 明显耗竭。在外源性添加 Tregs 的情况下,在集落形成和移植实验中,不足以挽救来自抗生素治疗的小鼠的骨髓功能。这些发现表明,肠道微生物群支持正常的 Treg 发育,以保护健康的造血,但仅恢复 Tregs 不足以恢复正常的骨髓功能。