Use of Autologous Bacteriotherapy to Treat Staphylococcus aureus in Patients With Atopic Dermatitis
Authors:
- 16 June 2021
- journal article
- research article
- Published by American Medical Association (AMA) in JAMA Dermatology
- Vol. 157 (8) , 978-982
Abstract
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:NCT03158012Keywords
This publication has 18 references indexed in Scilit:
- Antimicrobials from human skin commensal bacteria protect against Staphylococcus aureus and are deficient in atopic dermatitisScience Translational Medicine, 2017
- Faculty Opinions recommendation of Endogenous antimicrobial peptides and skin infections in atopic dermatitis.2015
- Commensal–dendritic-cell interaction specifies a unique protective skin immune signatureNature, 2015
- Temporal shifts in the skin microbiome associated with disease flares and treatment in children with atopic dermatitisGenome Research, 2012
- History of eczema herpeticum is associated with the inability to induce human β-defensin (HBD)-2, HBD-3 and cathelicidin in the skin of patients with atopic dermatitisBritish Journal of Dermatology, 2010
- Injury downregulates the expression of the human cathelicidin protein hCAP18/LL‐37 in atopic dermatitisExperimental Dermatology, 2010
- Mechanism of HBD-3 deficiency in atopic dermatitisClinical Immunology, 2006
- Cytokine Milieu of Atopic Dermatitis Skin Subverts the Innate Immune Response to Vaccinia VirusImmunity, 2006
- Endogenous Antimicrobial Peptides and Skin Infections in Atopic DermatitisNew England Journal of Medicine, 2002
- Staphylococcus aureus in the lesions of atopic dermatitisBritish Journal of Dermatology, 1974