Division of Dermatology and Venereology, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.
Pediatric Dermatology Unit, Dana Children's Hospital, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.
Immun Inflamm Dis. 2022 Mar;10(3):e570. doi: 10.1002/iid3.570. Epub 2021 Dec 20.
BACKGROUND: Atopic dermatitis (AD) is a remitting relapsing chronic eczematous pruritic disease. Several studies suggest that gut microbiota may influence AD by immune system regulation. METHODS: We performed the first in-human efficacy and safety assessment of fecal microbiota transplantation (FMT) for AD adult patients. All patients received 2 placebo transplantations followed by 4 FMTs each 2 weeks apart. AD severity and fecal microbiome profile were evaluated by the Scoring Atopic Dermatitis Score (SCORAD), the weekly frequency of topical corticosteroids usage, and gut microbiota metagenomic analysis, at the study beginning, before every FMT, and 1-8 months after the last FMT. RESULTS: Nine patients completed the study protocol. There was no significant change in the SCORAD score following the two placebo transplants. The average SCORAD score significantly decreased from baseline at Weeks 4-12 (before and 2 weeks after 4 times of FMT) (59.2 ± 34.9%, Wilcoxon p = .011), 50% and 75% decrease was achieved by 7 (77%) and 4 (44%) patients, respectively. At Week 18 (8 weeks after the last FMT) the average SCORAD score decreased from baseline at Week 4 (85.5 ± 8.4%, Wilcoxon p = .018), 50% and 75% decrease was achieved by 7 (77%) and 6 (66.7%) patients respectively. Weekly topical corticosteroids usage was diminished during the study and follow-up period as well. Two patients had a quick relapse and were switched to a different treatment. Two patients developed exacerbations alleviated after an additional fifth FMT. Metagenomic analysis of the fecal microbiota of patients and donors showed bacterial strains transmission from donors to patients. No adverse events were recorded during the study and follow-up period. CONCLUSIONS: FMT may be a safe and effective therapeutic intervention for AD patients, associated with transfer of specific microbial species from the donors to the patients. Further studies are required to reconfirm these results.
背景:特应性皮炎(AD)是一种反复发作的慢性湿疹性瘙痒性疾病。多项研究表明,肠道微生物群可能通过免疫系统调节影响 AD。
方法:我们对 AD 成年患者进行了粪便微生物群移植(FMT)的首次人体疗效和安全性评估。所有患者均接受 2 次安慰剂移植,随后每 2 周接受 4 次 FMT。在研究开始时、每次 FMT 前以及最后一次 FMT 后 1-8 个月,通过 SCORAD 评分(特应性皮炎评分)、每周外用皮质类固醇使用频率和肠道微生物组宏基因组分析评估 AD 严重程度和粪便微生物群谱。
结果:9 名患者完成了研究方案。在两次安慰剂移植后,SCORAD 评分没有显著变化。在第 4-12 周(4 次 FMT 前和 2 周后),平均 SCORAD 评分从基线显著下降(59.2±34.9%,Wilcoxon p=0.011),7 名(77%)和 4 名(44%)患者分别实现了 50%和 75%的下降。在第 18 周(最后一次 FMT 后 8 周),平均 SCORAD 评分从第 4 周的基线下降(85.5±8.4%,Wilcoxon p=0.018),7 名(77%)和 6 名(66.7%)患者分别实现了 50%和 75%的下降。在研究和随访期间,每周外用皮质类固醇的使用也减少了。两名患者迅速复发并改用其他治疗方法。两名患者出现加重,经额外的第五次 FMT 缓解。对患者和供体粪便微生物群的宏基因组分析显示,供体细菌株从供体转移到患者。在研究和随访期间未记录到不良事件。
结论:FMT 可能是 AD 患者的一种安全有效的治疗干预措施,与从供体向患者传递特定的微生物种类有关。需要进一步的研究来证实这些结果。
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