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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 3
2013 pubmed 166 citations

The human cathelicidin LL-37 has antiviral activity against respiratory syncytial virus.

Currie. Silke M SM; Findlay. Emily Gwyer EG; McHugh. Brian J BJ; Mackellar. Annie A; Man. Tian T; Macmillan. Derek D; Wang. Hongwei H; Fitch. Paul M PM; Schwarze. Jürgen J; Davidson. Donald J DJ

Key Findings

  • LL‑37 blocks RSV infection and prevents virus‑induced cell death in cultured airway cells
  • A shortened central fragment of LL‑37 retains antiviral activity
  • LL‑37 reduces production of new infectious RSV particles and limits spread of infection

Practical Outcomes

  • For now, the finding is mostly a proof‑of‑concept, but biohackers could explore ways to naturally raise LL‑37 levels (e.g., vitamin D, certain nutrients) while keeping an eye on emerging LL‑37‑based antivirals. Direct supplementation with LL‑37 isn’t ready for human use yet, but the study points to a potential new tool for RSV prevention or treatment.

Summary

The human antimicrobial peptide LL‑37 can stop RSV, a common cold‑like virus, from killing lung cells in lab dishes and cuts down the amount of new virus made. A smaller piece of the peptide works too, hinting that a drug could be built from it. While this is only an early‑stage lab result, it suggests that boosting LL‑37 naturally or using a synthetic version might help protect against RSV in the future.

Abstract

Respiratory syncytial virus is a leading cause of lower respiratory tract illness among infants, the elderly and immunocompromised individuals. Currently, there is no effective vaccine or disease modifying treatment available and novel interventions are urgently required. Cathelicidins are cationic host defence peptides expressed in the inflamed lung, with key roles in innate host defence against infection. We demonstrate that the human cathelicidin LL-37 has effective antiviral activity against RSV in vitro, retained by a truncated central peptide fragment. LL-37 prevented virus-induced cell death in epithelial cultures, significantly inhibited the production of new infectious particles and diminished the spread of infection, with antiviral effects directed both against the viral particles and the epithelial cells. LL-37 may represent an important targetable component of innate host defence against RSV infection. Prophylactic modulation of LL-37 expression and/or use of synthetic analogues post-infection may represent future novel strategies against RSV infection.

Study Information

Provider

pubmed

Year

2013

Date

2013-08-30T00:00:00.000Z

DOI

10.1371/journal.pone.0073659

Citations

166

References

52