Exploring the skin microbiome in atopic dermatitis pathogenesis and disease modification.

The Journal of allergy and clinical immunology • 2024 Jul • Vol 154, 31-41. PMID 38761999.

This review explains how changes in the skin’s normal bacteria may help worsen atopic dermatitis, especially when Staphylococcus aureus becomes too abundant. It summarizes earlier research suggesting that treatments aimed at restoring a healthier skin microbiome may help control disease, alongside other AD therapies.

Open PubMed Open DOI Open in EasyNIH search

What this paper found

This review explains how changes in the skin’s normal bacteria may help worsen atopic dermatitis, especially when Staphylococcus aureus becomes too abundant.

It summarizes earlier research suggesting that treatments aimed at restoring a healthier skin microbiome may help control disease, alongside other AD therapies.

What the paper is actually saying

Atopic dermatitis is common, and the abstract describes it as a disease with a weakened skin barrier influenced by genetic, chemical, immune, and microbial factors. Because skin microbes may actively worsen or improve the condition, the authors reviewed this area to consider whether the microbiome could be a treatment target.

The authors wanted to examine how the skin microbiome is involved in atopic dermatitis and what treatment approaches might modify the disease by changing the microbial environment.

This is a review article, not a single new experiment. The authors summarize prior research on how skin bacteria relate to AD and discuss treatment strategies aimed at changing the skin microbiome, skin pH, or immune signals.

The abstract argues that in AD, higher skin pH helps create conditions that favor overgrowth of Staphylococcus aureus. It also says that S aureus can release toxins and proteases that further damage the skin barrier and disturb immune balance, while helpful skin bacteria may restrain S aureus through quorum sensing. The review then outlines possible ways to modify disease by targeting these processes, including pH modulation, UV treatment, prebiotics, probiotics, postbiotics, microbiome transplantation, ozone therapy, phage therapy, and systemic immunomodulatory drugs and biologics.

The authors conclude that targeting the skin microbiome may become an important part of future atopic dermatitis treatment, but this paper is a summary of existing research rather than proof from one definitive trial.

What this abstract does not fully answer

This is a review article, so it summarizes previous studies rather than presenting one new controlled experiment.

The abstract does not describe how the authors selected or evaluated the earlier studies, so the review methods are unclear from the abstract alone.

The abstract discusses many possible treatments, including exploratory approaches, but it does not provide outcome data or quantify how well these approaches work.

Numbers the abstract makes important

This abstract did not highlight a small set of decision-relevant numbers.

Original abstract sections

Inflammatory skin diseases such as atopic eczema (atopic dermatitis [AD]) affect children and adults globally. In AD, the skin barrier is impaired on multiple levels. Underlying factors include genetic, chemical, immunologic, and microbial components. Increased skin pH in AD is part of the altered microbial microenvironment that promotes overgrowth of the skin microbiome with Staphylococcus aureus. The secretion of virulence factors, such as toxins and proteases, by S aureus further aggravates the skin barrier deficiency and additionally disrupts the balance of an already skewed immune response. Skin commensal bacteria, however, can inhibit the growth and pathogenicity of S aureus through quorum sensing. Therefore, restoring a healthy skin microbiome could contribute to remission induction in AD. This review discusses direct and indirect approaches to targeting the skin microbiome through modulation of the skin pH; UV treatment; and use of prebiotics, probiotics, and postbiotics. Furthermore, exploratory techniques such as skin microbiome transplantation, ozone therapy, and phage therapy are discussed. Finally, we summarize the latest findings on disease and microbiome modification through targeted immunomodulatory systemic treatments and biologics. We believe that targeting the skin microbiome should be considered a crucial component of successful AD treatment in the future.