医学
特应性皮炎
欺骗
随机对照试验
不利影响
葡萄球菌感染
临床试验
临床终点
皮肤病科
内科学
外科
金黄色葡萄球菌
遗传学
生物
程序设计语言
细菌
计算机科学
作者
Teruaki Nakatsuji,Richard L. Gallo,Faiza Shafiq,Yun Tong,Kimberly Chun,Anna M. Butcher,J Cheng,Tissa Hata
出处
期刊:JAMA Dermatology
[American Medical Association]
日期:2021-06-16
卷期号:157 (8): 978-978
被引量:36
标识
DOI:10.1001/jamadermatol.2021.1311
摘要
Importance
Atopic dermatitis (AD) can be negatively affected byStaphylococcus aureus. The skin microbiome of AD is deficient in coagulase-negativeStaphylococcus(CoNS) that can killS aureus. Objective
To evaluate if the antimicrobial-producing CoNS (CoNS-AM+) of a patient with AD can be autologously reintroduced to the same patient to inhibit survival ofS aureusand improve clinical outcomes. Design, Setting, and Participants
This double-blind, vehicle-controlled, single-center randomized clinical trial of 11 adult patients with moderate to severe AD who were randomized to receive either an autologous CoNS-AM+ (n = 5) or the vehicle (n = 6) was conducted between April 2016 and May 2018. The data were analyzed from May 2018 to July 2019. Interventions
Autologous CoNS-AM+ was isolated from swabs that were obtained from the nonlesional skin of each patient with AD, expanded by culture, and then reapplied topically to the forearms at a concentration of 107colony-forming units/g. Main Outcomes and Measures
The primary end point of this study was to assessS aureusabundance after 1 week of application of autologous CoNS-AM+ on patients with AD by culture-based and DNA-based methods. The secondary end points were to assess the safety and clinical outcomes. Results
Eleven patients (4 men [36.4%] and 7 women [63/6%]) were recruited based on the inclusion criteria. There were no serious adverse events in groups treated with autologous CoNS-AM+ or the vehicle.Staphylococcus aureuscolonization on lesional skin at the end of treatment on patients who were treated with autologous CoNS-AM+ (mean of log10 ratio to baseline, −1.702; 95% CI, −2.882 to −0.523) was reduced by 99.2% compared with vehicle treatment (mean of log10 ratio to baseline, 0.671; 95% CI, −0.289 to 1.613;P = .01) and persisted for 4 days after treatment (CoNS-AM+: mean of log10 ratio to baseline, −1.752; 95% CI, −3.051 to −0.453; vehicle: mean of log10 ratio to baseline, −0.003; 95% CI, −1.083 to 1.076;P = .03). Importantly, local Eczema Area And Severity Index scores that were assessed at day 11 on patients who received CoNS-AM+ (mean of percentage change, −48.45; 95% CI, −84.34 to −12.55) were significantly improved compared with vehicle treatment (mean of percentage change, −4.52; 95% CI, −36.25 to 27.22;P = .04). Conclusions and Relevance
The data from this randomized clinical trial suggest that bacteriotherapy with an autologous strain of skin commensal bacteria can safely decreaseS aureuscolonization and improve disease severity. Although larger studies will be needed, this personalized approach forS aureusreduction may provide an alternative treatment for patients with AD beyond antibiotics, immunosuppression, and immunomodulation. Trial Registration
ClinicalTrials.gov Identifier:NCT03158012
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