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通过使用益生菌和益生元进行肠道微生物群干预,可以诱导调节性 T 细胞,从而降低异基因造血干细胞移植后发生严重急性移植物抗宿主病的风险。

Gut microbiota intervention by pre and probiotics can induce regulatory T cells and reduce the risk of severe acute GVHD following allogeneic hematopoietic stem cell transplantation.

机构信息

Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.

Hematopoietic Stem Cell Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Transpl Immunol. 2023 Jun;78:101836. doi: 10.1016/j.trim.2023.101836. Epub 2023 Apr 8.

Abstract

BACKGROUND

Acute graft-versus-host disease (aGVHD) is one of the leading causes of limitation and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Numerous studies have shown that changes in the gut microbiome diversity increased post-transplant problems, including the occurrence of aGVHD. Probiotics and prebiotics can reconstitute the gut microbiota and thus increase bacterial metabolites such as short-chain fatty acids (SCFAs) that have immunomodulatory effects preventing aGVHD in recipients of allo-HSCTs.

METHODS/STUDY DESIGN: We conducted a pilot randomized clinical trial to investigate whether oral synbiotics are associated with the prevention or reduction in occurrence/severity and mitigate complications of aGVHD following allo-HSCT. A commercially available synbiotic mixture containing high levels of 7 safe bacterial strains plus fructo-oligosaccharides as a prebiotic was administered to allo-HSCT recipients. Out of 40 allo-HSCT patients, 20 received daily a synbiotic 21 days prior to transplantation (days -21 to day 0). In contrast, in the control group 20 recipients of allo-HSCT did not receive a symbiotic therapy.

RESULTS

Within first 100 days of observation, the incidence of severe (grade III/IV) aGVHD in the a synbiotic-therapy group was 0% (0 out of 20 patients), whereas it was 25% (5 out of 20 patients) in the control group (P = 0.047). The median percentage of CD4 + CD25 + Foxp3+ regulatory T cells (Tregs) among CD4+ lymphocytes on day 28 after HSCT in the synbiotic group was higher (2.54%) than in control group (1.73%; P = 0.01). There was no difference in Treg cells on day 7 after HSCT between two groups. However, the median percentage and the absolute count of Tregs in patients who experience aGVHD was significantly lower on days 7 and 28 after HSCT (both P < 0.05). The overall 12-month survival (OS) rate was higher (90%) in the symbiotic-treated patients than in the control group (75%), but the difference was not statistically significant (P = 0.234).

CONCLUSION

Our preliminary findings suggest that synbiotic intake before and during the conditioning regimen of allo-HSCT patients may lead to a reduction in the incidence and severity of aGVHD through the induction of CD4 + CD25 + Foxp3+ regulatory T cells, thus contributing to the improvement of transplant outcomes. Much larger studies are needed to confirm our observations.

摘要

背景

急性移植物抗宿主病(aGVHD)是异基因造血干细胞移植(allo-HSCT)后限制和死亡的主要原因之一。许多研究表明,移植后肠道微生物组多样性的变化增加了问题的发生,包括 aGVHD 的发生。益生菌和益生元可以重建肠道微生物群,从而增加具有免疫调节作用的细菌代谢物,如短链脂肪酸(SCFAs),从而预防 allo-HSCT 受者的 aGVHD。

方法/研究设计:我们进行了一项试点随机临床试验,以研究口服合生剂是否与预防或减少 allo-HSCT 后 aGVHD 的发生/严重程度和减轻其并发症有关。一种市售的合生剂混合物含有高水平的 7 种安全细菌株和作为益生元的低聚果糖,用于 allo-HSCT 受者。在 40 名 allo-HSCT 患者中,20 名患者在移植前 21 天(-21 天至 0 天)每天接受合生剂治疗。相比之下,对照组的 20 名 allo-HSCT 受者未接受合生剂治疗。

结果

在观察的前 100 天内,合生剂治疗组重度(III/IV 级)aGVHD 的发生率为 0%(20 名患者中无 1 例),而对照组为 25%(20 名患者中 5 例)(P=0.047)。在 HSCT 后 28 天,合生剂组 CD4+淋巴细胞中 CD4+CD25+Foxp3+调节性 T 细胞(Tregs)的中位数百分比(2.54%)高于对照组(1.73%;P=0.01)。两组患者在 HSCT 后 7 天的 Treg 细胞无差异。然而,在发生 aGVHD 的患者中,第 7 天和第 28 天的 Treg 细胞中位数和绝对计数明显较低(均 P<0.05)。在合生剂治疗组中,12 个月总生存率(OS)为 90%,高于对照组的 75%,但差异无统计学意义(P=0.234)。

结论

我们的初步发现表明,在 allo-HSCT 患者的预处理和治疗期间摄入合生剂可能通过诱导 CD4+CD25+Foxp3+调节性 T 细胞来降低 aGVHD 的发生率和严重程度,从而改善移植结果。需要更大规模的研究来证实我们的观察结果。

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