Probiotics and Eczema: Exploring the Gut-Skin Axis

Probiotics and Eczema: Exploring the Gut-Skin Axis

Atopic dermatitis is the most common form of eczema. It is an inflammatory skin condition characterised by dry, itchy skin that is prone to infection1. In recent years, a link between gut health and eczema has been recognised, highlighting the potential of probiotics to help manage eczema symptoms2. Read on to explore how probiotics may help support the gut and skin microbiomes and their potential role in eczema symptom management.

Eczema (atopic dermatitis): pathophysiology overview

The pathophysiology of eczema is driven by genetics, dysfunction of the skin barrier and the immune system.

Genetic mutations can alter the outermost layer of skin. This reduces ceramides, moisturising factors and antimicrobial peptides, resulting in increased skin pH and moisture loss. Dry, itchy skin is vulnerable to allergens and microbial invasion, particularly Staphylococcus aureus. This triggers the immune system to attack the skin, further breaking down the skin barrier and resulting in fewer fats and proteins that maintain skin barrier function, which can trigger eczema flare-ups and symptoms3.

Eczema is mainly treated with moisturisers to repair the skin barrier and anti-inflammatory agents. Newer strategies are investigating the link between the gut and the skin to help regulate inflammation and microbial imbalance, which may support symptom control and flare-ups4.

The gut–skin axis

The gut–skin axis describes the bidirectional communication between the gut and skin, including interactions between the gut and the atopic dermatitis microbiome.

Through our diet, we come into contact with many inflammatory mediators such as lipopolysaccharides, which can be found in high-fat meat and dairy products5. These enter our bloodstream through the intestine, sparking whole-body inflammatory processes and exacerbating the pathways involved in eczema flare-ups6.

Meanwhile, microbial metabolites produced by the gut, particularly short-chain fatty acids such as butyrate and propionate, help reduce inflammation and can enhance the skin barrier, relieving eczema symptoms7.

Gut dysbiosis in eczema

Gut dysbiosis refers to an imbalance in gut microbiota, often with fewer beneficial bacteria, leading to overgrowth of harmful bacteria and inflammation. This can contribute to skin barrier dysfunction and eczema flare-ups8.

Early colonisation of the gut microbiome relies heavily on key vaginal microbes that infants are exposed to during birth. Caesarean births reduce exposure to maternal vaginal flora, lowering beneficial bacterial colonisation and increasing the risk of gut dysbiosis. Prenatal or neonatal antibiotic use can also disrupt bacterial colonies9.

This link between gut health and eczema is further highlighted by the fact that early colonisation with beneficial bacteria is associated with a reduced risk of childhood eczema, which occurs more frequently in caesarean-born children10.

Probiotic strains studied in eczema

Widely studied probiotic strains for eczema include Lactobacillus rhamnosus GG (LGG) and Bifidobacterium species to help modulate the gut and skin microbiomes. LGG reduces inflammation, promotes skin barrier health through the production of short-chain fatty acids, and supports a more beneficial gut and skin microbiome profile11. Bifidobacterium species may play a key role in eczema prevention by restoring early-life gut microbiota balance, reducing inflammation and supporting skin barrier health12.

Multi-strain probiotic formulas mimic the diverse gut microbiome population and may offer complementary benefits. For example, LGG’s anti-inflammatory and skin barrier repair effects may be enhanced by Bifidobacterium properties. These formulas can better address dysbiosis across the gut and skin, and may potentially help control eczema flare-ups13.

The best probiotic products for managing eczema: what does the clinical evidence show?

Lactobacillus-based probiotics

  • Lactobacillus rhamnosus GG (LGG): After 12 weeks of daily use, children aged 6–36 months experienced fewer eczema flare-ups and improvements in both their gut and skin microbiome populations11.
  • Lactobacillus rhamnosus HN001: When taken by mothers from late pregnancy, around 35 weeks, through 6 months of breastfeeding, and by their children from birth to age 2, this probiotic lowered the long-term risks of eczema, allergies and hay fever up to age 1114.
  • Lactobacillus salivarius LS01: Adults who took this probiotic daily for 16 weeks showed fewer eczema symptoms, a healthier gut microbiome and reduced inflammation compared with those taking a placebo15.
  • Lactobacillus acidophilus: Adults over the age of 16 who took oral probiotics for 8 weeks experienced improved eczema symptoms and inflammation16.

Other single-strain probiotics

  • Bifidobacterium longum: Children aged 3–12 months used the oral probiotic alongside antihistamines and emollients for 8 weeks. This led to a 60% reduction in eczema symptoms, an improved gut microbiome and reduced inflammation17.
  • Roseomonas mucosa: In children under 7, topical application improved the skin barrier, lowered Staphylococcus aureus levels, reduced the need for steroids, and improved gut and skin microbiomes for up to 8 months after treatment18.

Mixed-strain probiotics

  • Lactobacillus paracasei LPC-37, Lactobacillus rhamnosus HN001, Lactobacillus acidophilus NCFM and Bifidobacterium lactis HN019: Daily supplementation in children aged 6 months to 19 years with eczema over 6 months led to improved symptoms19.
  • Lactobacillus rhamnosus LC705, Bifidobacterium breve Bb99 and Propionibacterium freudenreichii ssp. shermanii JS: In caesarean-delivered children, daily perinatal probiotics resulted in fewer children developing eczema20.
  • Bifidobacterium longum, Lactobacillus acidophilus and Enterococcus faecalis: Eczema symptoms significantly improved after 4 months in infants up to 11 months old21.
  • Bifidobacterium lactis CECT 8145, Bifidobacterium longum CECT 7347 and Lactobacillus casei CECT 9104: After 12 weeks of probiotic use, the need for topical steroids to treat eczema flare-ups was reduced22.

Safety and clinical considerations

Probiotic strains for eczema are generally safe for most people. However, they can interact with the host’s existing microbiota, occasionally causing mild gastrointestinal symptoms such as bloating or discomfort. Clinical evidence indicates that not all probiotic strains are equally effective. Some strains appear effective at preventing or managing eczema symptoms, while others show little to no change2.

In certain high-risk populations, including those who are immunodeficient, neonates or those with severe health issues, probiotics should be used with caution. There have been rare but serious reports of allergic reactions23, bacterial or fungal infection, and even sepsis24.

Practical considerations for HCPs

When recommending probiotics for eczema, patient safety should be prioritised. Probiotics are generally safe for low-risk, healthy individuals, but should be avoided in patients who are severely immunocompromised, are ill or have multiple risk factors25.

For eligible patients, the potential effectiveness of probiotics may depend on the strain and quality control. Recommended probiotics should have peer-reviewed clinical evidence with verified colony-forming units (CFUs) to support potency claims26. The quality, dose and duration of use are critical and may determine how effective the probiotic will be.

Probiotics may have a valuable role alongside standard eczema creams and anti-inflammatory treatments. They have been shown to be particularly effective for the prevention of eczema or in cases where underlying gut dysbiosis is identified as a driver of systemic inflammation24.

Finally, managing patient expectations is essential. Any potential symptom improvement will not be immediate and may take a few weeks or months, depending on the specific strain and dosage24. Regular monitoring and follow-up assessments are vital to ensure the treatment is working, identify any side effects early, and improve outcomes.

References

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  2. Makrgeorgou A, Leonardi‐Bee J, Bath‐Hextall FJ, Murrell DF, Tang ML, Roberts A, et al. Probiotics for treating eczema. Cochrane Database Syst Rev. 2018;2018(11):CD006135.
  3. Kim J, Kim BE, Leung DYM. Pathophysiology of atopic dermatitis: clinical implications. Allergy Asthma Proc. 2019;40(2):84–92.
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  7. Nambidi S, Sennie NS, Kondaveeti SB, Banerjee A, Pathak S, Duttaroy AK. A review of short-chain fatty acids in gut and skin: possible implications in skin aging. J Funct Foods. 2025;133:107010.
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  11. Carucci L, Nocerino R, Paparo L, De Filippis F, Coppola S, Giglio V, et al. Therapeutic effects elicited by the probiotic Lacticaseibacillus rhamnosus GG in children with atopic dermatitis: the results of the ProPAD trial. Pediatr Allergy Immunol. 2022;33(8):e13836.
  12. Marras L, Caputo M, Bisicchia S, Soato M, Bertolino G, Vaccaro S, et al. The role of bifidobacteria in predictive and preventive medicine: a focus on eczema and hypercholesterolaemia. Microorganisms. 2021;9(4):836.
  13. Bakkeren E, Piskovsky V, Lee MNY, Jahn MT, Foster KR. Strain displacement in microbiomes via ecological competition. Nat Microbiol. 2025;10(12):3122–35.
  14. Wickens K, Barthow C, Mitchell EA, Kang J, van Zyl N, Purdie G, et al. Effects of Lactobacillus rhamnosus HN001 in early life on the cumulative prevalence of allergic disease to 11 years. Pediatr Allergy Immunol. 2018;29(8):808–14.
  15. Drago L, Iemoli E, Rodighiero V, Nicola L, De Vecchi E, Piconi S. Effects of Lactobacillus salivarius LS01 (DSM 22775) treatment on adult atopic dermatitis: a randomised placebo-controlled study. Int J Immunopathol Pharmacol. 2011;24(4):1037–48.
  16. Inoue Y, Kambara T, Murata N, Komori-Yamaguchi J, Matsukura S, Takahashi Y, et al. Effects of oral administration of Lactobacillus acidophilus L-92 on the symptoms and serum cytokines of atopic dermatitis in Japanese adults: a double-blind, randomised clinical trial. Int Arch Allergy Immunol. 2014;165(4):247–54.
  17. Lisiecka MZ. Novel therapeutic approaches for treating moderate-to-severe atopic dermatitis in infants with polyvalent allergic sensitisation. J Mother Child. 30(1):33–43.
  18. Myles IA, Castillo CR, Barbian KD, Kanakabandi K, Virtaneva K, Fitzmeyer E, et al. Therapeutic responses to Roseomonas mucosa in atopic dermatitis may involve lipid-mediated TNF-related epithelial repair. Sci Transl Med. 2020;12(560):eaaz8631.
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  20. Kuitunen M, Kukkonen K, Juntunen-Backman K, Korpela R, Poussa T, Tuure T, et al. Probiotics prevent IgE-associated allergy until age 5 years in caesarean-delivered children but not in the total cohort. J Allergy Clin Immunol. 2009;123(2):335–41.
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