Literature DB >> 34132739

Use of Autologous Bacteriotherapy to Treat Staphylococcus aureus in Patients With Atopic Dermatitis: A Randomized Double-blind Clinical Trial.

Teruaki Nakatsuji1, Richard L Gallo1, Faiza Shafiq1, Yun Tong1, Kimberly Chun1, Anna M Butcher1, Joyce Y Cheng1, Tissa R Hata1.   

Abstract

IMPORTANCE: Atopic dermatitis (AD) can be negatively affected by Staphylococcus aureus. The skin microbiome of AD is deficient in coagulase-negative Staphylococcus (CoNS) that can kill S 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 of S aureus and 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 107 colony-forming units/g. MAIN OUTCOMES AND MEASURES: The primary end point of this study was to assess S aureus abundance 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 aureus colonization 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 decrease S aureus colonization and improve disease severity. Although larger studies will be needed, this personalized approach for S aureus reduction may provide an alternative treatment for patients with AD beyond antibiotics, immunosuppression, and immunomodulation. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03158012.

Entities:  

Year:  2021        PMID: 34132739      PMCID: PMC8209585          DOI: 10.1001/jamadermatol.2021.1311

Source DB:  PubMed          Journal:  JAMA Dermatol        ISSN: 2168-6068            Impact factor:   11.816


  15 in total

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2.  Staphylococcus aureus in the lesions of atopic dermatitis.

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4.  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 dermatitis.

Authors:  T R Hata; P Kotol; M Boguniewicz; P Taylor; A Paik; M Jackson; M Nguyen; F Kabigting; J Miller; M Gerber; D Zaccaro; B Armstrong; R Dorschner; D Y M Leung; R L Gallo
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Authors:  Ian A Myles; Carlo R Castillo; Kent D Barbian; Kishore Kanakabandi; Kimmo Virtaneva; Emily Fitzmeyer; Monica Paneru; Francisco Otaizo-Carrasquero; Timothy G Myers; Tovah E Markowitz; Ian N Moore; Xue Liu; Marc Ferrer; Yosuke Sakamachi; Stavros Garantziotis; Muthulekha Swamydas; Michail S Lionakis; Erik D Anderson; Noah J Earland; Sundar Ganesan; Ashleigh A Sun; Jenna R E Bergerson; Robert A Silverman; Maureen Petersen; Craig A Martens; Sandip K Datta
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6.  Non-classical Immunity Controls Microbiota Impact on Skin Immunity and Tissue Repair.

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7.  Cytokine milieu of atopic dermatitis skin subverts the innate immune response to vaccinia virus.

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Journal:  Immunity       Date:  2006-03       Impact factor: 31.745

8.  Injury downregulates the expression of the human cathelicidin protein hCAP18/LL-37 in atopic dermatitis.

Authors:  Lotus Mallbris; Lina Carlén; Tianling Wei; Johan Heilborn; Margareta Frohm Nilsson; Fredrik Granath; Mona Ståhle
Journal:  Exp Dermatol       Date:  2009-07-23       Impact factor: 3.960

9.  Commensal-dendritic-cell interaction specifies a unique protective skin immune signature.

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Journal:  Nature       Date:  2015-01-05       Impact factor: 49.962

10.  Development of a human skin commensal microbe for bacteriotherapy of atopic dermatitis and use in a phase 1 randomized clinical trial.

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Journal:  Nat Med       Date:  2021-02-22       Impact factor: 53.440

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