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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 1
2024 pubmed 1 citations

Antimicrobial peptides and other potential biomarkers of critical illness in SARS-CoV-2 patients with acute kidney injury. AMPAKI-CoV study.

Theotonio Dos Santos. Lucas Ferreira LF; Barbeiro. Hermes Vieira HV; Barbeiro. Denise Frediani DF; de Souza. Heraldo Possolo HP; Pinheiro da Silva. Fabiano F

Key Findings

  • Alpha‑defensin 1 and 3 levels were significantly higher in COVID‑19 patients, especially those with acute kidney injury (AKI).
  • Inflammatory cytokines such as IL‑6, IL‑10, IFN‑γ and MCP‑1 were elevated in the COVID‑19 groups compared to healthy controls.
  • IL‑10 and the IL‑10×IL‑1B ratio distinguished AKI patients well (AUC ≈ 0.86‑0.88), but LL‑37 levels were not highlighted as changed.

Practical Outcomes

  • At present there’s no actionable protocol for LL‑37 supplementation or dosing. The findings mainly point to a role of other antimicrobial peptides and cytokines in COVID‑19 severity, suggesting more research is needed before biohackers can apply this information.

Summary

The study measured several antimicrobial peptides, including LL‑37, in COVID‑19 patients with and without kidney injury. It found that other peptides (alpha‑defensins) and inflammatory cytokines were higher in sick patients, but it didn’t show any clear benefit or dosage guidance for LL‑37, so there’s nothing immediately useful for self‑experiments.

Abstract

Antimicrobial peptides (AMPs) constitute a complex network of 10-100 amino acid sequence molecules widely distributed in nature. While over 300 AMPs have been described in mammals, cathelicidins and defensins remain the most extensively studied. Some publications have explored the role of AMPs in COVID-19, but these findings are preliminary, and in vivo studies are still lacking. In this study, we report the plasma levels of five AMPs (LL-37, α-defensin 1, α-defensin 3, β-defensin 1, and β-defensin 3), using the ELISA technique (MyBioSource, San Diego, CA, United States, kits MBS2601339 (beta-defensin 1), MBS2602513 (beta-defensin 3), MBS703879 (alpha-defensin 1), MBS706289 (alpha-defensin 3), MBS7234921 (LL37)), and the measurement of six cytokines (tumor necrosis factor-α, interleukin-1β, interleukin-6, interleukin-10, interferon-γ, and monocyte chemoattractant protein-1), through the magnetic bead immunoassay Milliplex® and the MAGPIX® System (MilliporeSigma, Darmstadt, Germany, kit HCYTOMAG-60 K (cytokines)), in 15 healthy volunteers, 36 COVID-19 patients without Acute Kidney Injury (AKI) and 17 COVID-19 patients with AKI. We found increased levels of α-defensin 1, α-defensin 3 and β-defensin 3, in our COVID-19 population, when compared to healthy controls, along with higher levels of interleukin-6, interleukin-10, interferon-γ, and monocyte chemoattractant protein-1. These findings suggest that these AMPs and cytokines may play a crucial role in the systemic inflammatory response and tissue damage characterizing severe COVID-19. The levels of α-defensin 1 and α-defensin 3 were significantly higher in COVID-19 AKI group in comparison to the non-AKI group. Furthermore, IL-10 and the product IL-10 × IL-1B showed excellent performance in discriminating AKI, with AUCs of 0.86 and 0.88, respectively. Among patients with COVID-19, AMPs may play a key role in the inflammation process and disease progression. Additionally, α-defensin 1 and α-defensin 3 may mediate the AKI process in these patients, representing an opportunity for further research and potential therapeutic alternatives in the future.

Study Information

Provider

pubmed

Year

2024

Date

2024-02-01T00:00:00.000Z

DOI

10.14814/phy2.15945

Citations

1

References

35