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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 2
2024 pubmed 7 citations

Pro-inflammatory activity of Cutibacterium acnes phylotype IA<sub>1</sub> and extracellular vesicles: An in&#xa0;vitro study.

Cheung. Caroline T CT; Lancien. Ugo U; Corvec. St&#xe9;phane S; Mengeaud. Val&#xe9;rie V; Mias. C&#xe9;line C; V&#xe9;ziers. Jo&#xeb;lle J; Khammari. Amir A; Dr&#xe9;no. Brigitte B

Key Findings

  • EVs from C. acnes strain taken from acne lesions increase LL‑37 and several inflammatory cytokines in skin cells
  • EVs from a strain taken from healthy skin cause a much weaker inflammatory response
  • This is the first evidence that different C. acnes strains produce distinct EVs that affect skin inflammation

Practical Outcomes

  • For DIY health enthusiasts, the work hints that modulating skin bacteria—through probiotics, targeted cleansers, or anti‑bacterial strategies—might influence LL‑37 levels and acne inflammation, but the study is in vitro and doesn’t provide specific treatment protocols.

Summary

The study shows that tiny particles (extracellular vesicles) released by acne‑related bacteria can boost the skin's natural antimicrobial peptide LL‑37, but they also raise inflammation markers. Vesicles from acne lesions cause a stronger response than those from normal skin, suggesting the bacteria’s strain matters for skin inflammation.

Abstract

Acne is a chronic inflammatory skin condition that involves Cutibacterium acnes (C. acnes), which is classified into six main phylotypes (IA<sub>1</sub>, IA<sub>2</sub>, IB, IC, II and III). Acne development is associated with loss of C. acnes phylotype diversity, characterised by overgrowth of phylotype IA<sub>1</sub> relative to other phylotypes. It was also shown that purified extracellular vesicles (EVs) secreted by C. acnes can induce an acne-like inflammatory response in skin models. We aimed to determine if the inflammatory profile of EVs secreted by C. acnes phylotype IA<sub>1</sub> from an inflammatory acne lesion was different from C. acnes phylotype IA<sub>1</sub> from normal skin, thus playing a direct role in the severity of inflammation. EVs were produced in&#xa0;vitro after culture of two clinical strains of C. acnes phylotype IA<sub>1</sub>, T5 from normal human skin and A47 from an inflammatory acne lesion, and then incubated with either human immortalised keratinocytes, HaCaT cells, or skin explants obtained from abdominoplasty. Subsequently, quantitative PCR (qPCR) was performed for human &#x3b2;-defensin 2 (hBD2), cathelicidin (LL-37), interleukin (IL)-1&#x3b2;, IL-6, IL-8, IL-17&#x3b1; and IL-36&#x3b3;, and ELISA for IL-6, IL-8 and IL-17&#x3b1;. We found that EVs produced in&#xa0;vitro by C. acnes derived from inflammatory acne lesions significantly increased the pro-inflammatory cytokines and anti-microbial peptides at both transcriptional and protein levels compared with EVs derived from normal human skin. We show for the first time that C. acnes EVs from inflammatory acne play a crucial role in acne-associated inflammation in&#xa0;vitro and that C. acnes phylotype IA<sub>1</sub> collected from inflammatory acne lesion and normal skin produce different EVs and inflammatory profiles in&#xa0;vitro.

Study Information

Provider

pubmed

Year

2024

Date

2024-08-01T00:00:00.000Z

DOI

10.1111/exd.15150

Citations

7

References

38