[Post-therapeutic change of cathelicidin LL-37 in asthmatics of different inflammatory phenotypes].
Liang. Zhen-yu ZY; Zhao. Hai-jin HJ; Lü. Yan-hua YH; Dong. Hang-ming HM; Liu. Lai-yu LY; Zhu. Shun-fang SF; Cai. Shao-xi SX
Key Findings
- Before treatment, LL‑37 levels were similar in asthma patients and healthy controls.
- After one month of budesonide/formoterol, LL‑37 increased in plasma and sputum of eosinophilic asthma patients.
- No significant LL‑37 change was seen in non‑eosinophilic asthma, and the post‑treatment LL‑37 levels no longer correlated with lung function measures.
Practical Outcomes
- For most biohackers, this study doesn’t provide a clear, actionable protocol for using LL‑37. It suggests that inhaled steroids can alter LL‑37 levels in a specific asthma subtype, but there’s no evidence of performance or longevity benefits. Until more research clarifies any functional impact, LL‑37 supplementation or targeting isn’t recommended for general health optimization.
Summary
A small study looked at how levels of the natural peptide LL‑37 change in people with asthma after a month of inhaled steroid/bronchodilator treatment. Overall, LL‑37 went up in the blood and sputum of patients with eosinophilic (allergy‑driven) asthma, but not in those with non‑eosinophilic asthma. The rise didn’t clearly link to better lung function, so it’s unclear if this matters for health or performance.
Abstract
To explore the post-therapeutic change of cathelicidin LL-37 in asthmatics of different inflammatory phenotypes. Thirty-four patients with initially diagnosed asthma (asthma group) and 14 normal subjects (control group) were recruited at Nanfang Hospital from August 2009 to August 2010 for this prospective study. Sputum and venous blood samples were collected and analyzed for cell differential. Eosinophilic asthma was defined as the count of sputum eosinophils ≥ 3%. The LL-37 concentrations in plasma and sputum supernatant were measured by enzyme-linked immunosorbent assay (ELISA) kit. The subjects were treated with budesonide/formoterol (160/4.5 µg) one inhalation twice daily and re-examined after 1 month. Prior to treatment, there were no differences between the asthma and control groups in the levels of LL-37 in plasma and sputum supernatant (P = 0.427,0.427). The plasma concentrations of LL-37 in asthma group were negatively correlated with baseline forced expiratory volume in one second (FEV(1), r = -0.470, P = 0.005), percent predicted of FEV(1) (FEV(1)%pred, r = -0.421, P = 0.013) and forced vital capacity (FVC, r = -0.367, P = 0.033). After treatment, the plasma and sputum supernatant concentrations of LL-37 (M (Q(R))) in the asthma group (5.6 (16.2), 65.6 (184.0) µg/L) were significantly higher than those baseline concentrations (5.03 (9.21), 28.40(109.76) µg/L, P = 0.005, 0.015). In the eosinophilic asthma subgroup, the plasma and sputum supernatant concentrations of LL-37 (M (Q(R))) after treatment (5.3 (19.3), 65.6 (185.2) µg/L) were significantly higher than those baseline concentrations (6.7 (8.9) L, 35.3 (102.0) µg/L, P = 0.021,0.014). And in the non-eosinophilic asthma subgroup, the changes of plasma and sputum supernatant concentrations of LL-37 showed no significant differences (P = 0.139, 0.386). In the asthma group, the correlations between plasma concentrations of LL-37 and FEV(1), FEV(1)%pred, FVC were not statistically significant (P = 0.283, 0.706,0.272) after treatment. LL-37 may participate in the aggravation of asthma. The elevated concentrations of LL-37 in eosinophilic asthma is probably due to the resolved suppression of LL-37 expression by eosinophilic inflammation. But its mechanism needs further researches.
Study Information
pubmed
2012
2012-03-27T00:00:00.000Z