The Rheumatism Research Center, Catholic Research Institute of Medical Science, College of Medicine, The Catholic University of Korea, 222, Banpo-daero, Seocho-gu, Seoul, 06591, Republic of Korea.
Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, 222, Banpo-daero, Seocho-gu, Seoul, 06591, Republic of Korea.
J Transl Med. 2022 Feb 25;20(1):104. doi: 10.1186/s12967-022-03303-z.
Graft-versus-host disease (GvHD) is a critical complication after allogeneic hematopoietic stem cell transplantation (HSCT). The immunosuppressants given to patients undergoing allogeneic HSCT disturb the microbiome and the host immune system, potentially leading to dysbiosis and inflammation, and may affect immune function and bone marrow transplantation. The intestinal microbiome is a target for the development of novel therapies for GvHD. Lactobacillus species are widely used supplements to induce production of antimicrobial and anti-inflammatory factors.
We determined the effect of the combination of Lactobacillus acidophilus and FK506 on GvHD following major histocompatibility complex-mismatched bone marrow transplantation.
The combination treatment suppressed IFN-γ and IL-17-producing T cell differentiation, but increased Foxp3Treg differentiation and IL-10 production. Also, the combination treatment and combination treated-induced Treg cells modulated the proliferation of murine alloreactive T cells in vitro. Additionally, the combination treatment upregulated Treg-related genes-Nt5e, Foxp3, Ikzf2, Nrp1 and Itgb8-in murine CD4-T cells. The combination treatment also alleviated GvHD clinically and histopathologically by controlling the effector T cell and Treg balance in vivo. Moreover, the combination treatment decreased Th17 differentiation significantly and significantly upregulated Foxp3 and IL-10 expression in peripheral blood mononuclear cells from healthy controls and liver transplantation (LT) patients.
Therefore, the combination of L. acidophilus and FK506 is effective and safe for patients undergoing allogeneic hematopoietic stem cell transplantation.
移植物抗宿主病(GvHD)是异基因造血干细胞移植(HSCT)后的一个关键并发症。接受异基因 HSCT 的患者使用的免疫抑制剂会干扰微生物组和宿主免疫系统,可能导致微生态失调和炎症,并可能影响免疫功能和骨髓移植。肠道微生物组是开发 GvHD 新疗法的目标。乳杆菌属是广泛使用的补充剂,可诱导产生抗菌和抗炎因子。
我们确定了嗜酸乳杆菌和 FK506 联合使用对主要组织相容性复合物不匹配的骨髓移植后 GvHD 的影响。
联合治疗抑制了 IFN-γ 和 IL-17 产生的 T 细胞分化,但增加了 Foxp3Treg 分化和 IL-10 的产生。此外,联合治疗和联合治疗诱导的 Treg 细胞调节了体外小鼠同种反应性 T 细胞的增殖。此外,联合治疗还通过体内控制效应 T 细胞和 Treg 平衡,在临床上和组织病理学上缓解 GvHD。此外,联合治疗可显著抑制 Th17 分化,并显著上调健康对照和肝移植(LT)患者外周血单个核细胞中 Foxp3 和 IL-10 的表达。
因此,嗜酸乳杆菌和 FK506 的联合使用对接受异基因造血干细胞移植的患者是有效且安全的。