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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 2
2015 pubmed 157 citations

Inflammatory Diseases of the Lung Induced by Conventional Cigarette Smoke: A Review.

Crotty Alexander. Laura E LE; Shin. Stephanie S; Hwang. John H JH

Key Findings

  • Cigarette smoke activates multiple inflammatory pathways (NF‑κB, AMPK, JNK, p38, STAT3) in airway cells.
  • LL‑37 and other antimicrobial peptides are found in higher amounts in the lungs of smokers.
  • Elevated LL‑37 is associated with various smoking‑related lung diseases such as COPD and interstitial lung disorders.

Practical Outcomes

  • For biohackers, the main takeaway is that smoking raises LL‑37 levels, which may contribute to lung inflammation rather than provide a clear health benefit. This suggests that avoiding cigarette smoke is important for lung health, and any attempts to modulate LL‑37 should await more specific research on its role and therapeutic targeting.

Summary

The review explains that smoking triggers a cascade of inflammatory signals in the lungs, leading to higher levels of several proteins, including the antimicrobial peptide LL‑37. While LL‑37 is part of the body’s immune response, its increase is linked to lung inflammation and disease in smokers.

Abstract

Smoking-induced lung diseases were extremely rare prior to the 20th century. With commercialization and introduction of machine-made cigarettes, worldwide use skyrocketed and several new pulmonary diseases have been recognized. The majority of pulmonary diseases caused by cigarette smoke (CS) are inflammatory in origin. Airway epithelial cells and alveolar macrophages have altered inflammatory signaling in response to CS, which leads to recruitment of lymphocytes, eosinophils, neutrophils, and mast cells to the lungs-depending on the signaling pathway (nuclear factor-κB, adenosine monophosphate-activated protein kinase, c-Jun N-terminal kinase, p38, and signal transducer and activator of transcription 3) activated. Multiple proteins are upregulated and secreted in response to CS exposure, and many of these have immunomodulatory activities that contribute to disease pathogenesis. In particular, metalloproteases 9 and 12, surfactant protein D, antimicrobial peptides (LL-37 and human β defensin 2), and IL-1, IL-6, IL-8, and IL-17 have been found in higher quantities in the lungs of smokers with ongoing inflammation. However, many underlying mechanisms of smoking-induced inflammatory diseases are not yet known. We review here the known cellular and molecular mechanisms of CS-induced diseases, including COPD, respiratory bronchiolitis-interstitial lung disease, desquamative interstitial pneumonia, acute eosinophilic pneumonia, chronic rhinosinusitis, pulmonary Langerhans cell histiocytosis, and chronic bacterial infections. We also discuss inflammation induced by secondhand and thirdhand smoke exposure and the pulmonary diseases that result. New targeted antiinflammatory therapeutic options are currently under investigation and hopefully will yield promising results for the treatment of these highly prevalent smoking-induced diseases.

Study Information

Provider

pubmed

Year

2015

Date

2015-11-01T00:00:00.000Z

DOI

10.1378/chest.15-0409

Citations

157

References

140