Anti-fungal activity of cathelicidins and their potential role in Candida albicans skin infection.
López-García. Belén B; Lee. Phillip H A PH; Yamasaki. Kenshi K; Gallo. Richard L RL
Key Findings
- LL-37 and mouse cathelicidin mCRAMP can kill C. albicans in vitro
- Fungicidal activity improves in sweat‑like ionic conditions and with cleavage products such as RK‑31
- Cathelicidin induction in skin doesn’t boost systemic or deep‑tissue resistance in mice
Practical Outcomes
- Topical products containing LL‑37 or its active fragments (e.g., RK‑31) might help prevent or treat superficial yeast infections, especially in sweaty areas. However, systemic use is unlikely to be effective, and delivery methods need to ensure the peptide reaches the skin surface in the right ionic environment.
Summary
LL-37, a natural human peptide, can kill the fungus Candida albicans on the skin, especially when it’s broken down into smaller pieces like RK‑31 and when the environment mimics sweat. It works by poking holes in the fungal membrane, but it doesn’t seem to protect the body from deeper infections. This means it could be useful as a topical antifungal, but it isn’t a cure for systemic yeast problems.
Abstract
Cathelicidins have broad anti-microbial capacity and are important for host defense against skin infections by some bacterial and viral pathogens. This study investigated the activity of cathelicidins against Candida albicans. The human cathelicidin LL-37, and mouse cathelicidin mCRAMP, killed C. albicans, but this fungicidal activity was dependent on culture conditions. Evaluation of the fungal membrane by fluorescent dye penetration after incubation with cathelicidins correlated membrane permeabilization and inhibition of fungal growth. Anti-fungal assays carried out in an ionic environment that mimicked human sweat and with the processed forms of cathelicidin such as are present in sweat found that the cleavage of LL-37 to forms such as RK-31 conferred additional activity against C. albicans. C. albicans also induced an increase in the expression of cathelicidin in mouse skin, but this induction did not confer systemic or subcutaneous resistance as mCRAMP-deficient mice were not more susceptible to C. albicans in blood-killing assays or in an intradermal infection model. Therefore, cathelicidins appear active against C. albicans, but may be most effective as a superficial barrier to infection.
Study Information
pubmed
2005
10.1111/j.0022-202x.2005.23713.x