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Study 15 of 17Thymosin Alpha-1 literatureNature medicine · Observational · PreclinicalTop journal2018

F508del-CFTR is not corrected by thymosin α1.

Thymosin α1 does not correct the F508del-CFTR defect in human airway epithelial cells, indicating it may not be a viable treatment option for this cystic fibrosis mutation.

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Where it sits

this study against the rest of the thymosin alpha-1 corpus
2
Preclinical
12
Observational · this one
0
Open-label
2
Randomised
1
Reviews

Summary and findings

This study investigates the effect of thymosin α1 on F508del-CFTR, a mutation associated with cystic fibrosis. The research was conducted in a cellular model, specifically using human airway epithelial cells. The findings indicate that thymosin α1 does not correct the F508del-CFTR defect.

How much of this paper we could read: partial text (0.50). We had some abstract detail. Check the source for anything decisive. What this means →
Preclinical2018

Background

The study addresses the potential of thymosin α1 to correct the F508del-CFTR mutation, which is a common cause of cystic fibrosis. Prior research has suggested various agents might restore function to defective CFTR proteins, but the efficacy of thymosin α1 in this context was unclear. This study is significant as it directly tests the hypothesis in a relevant cellular model.

Methods

The study employed a cellular model using human airway epithelial cells to assess the effect of thymosin α1 on F508del-CFTR. Specific details regarding the dose, duration, and primary or secondary outcome measures are not reported in the abstract.

Results

The primary endpoint indicated that thymosin α1 did not correct the F508del-CFTR defect, but specific numeric findings are not provided in the abstract.

Interpretation

These findings suggest that thymosin α1 does not have the desired corrective effect on F508del-CFTR, contrasting with other potential treatments that have shown varying degrees of success. The lack of correction implies limited clinical relevance for thymosin α1 in treating cystic fibrosis related to this mutation. The absence of detailed numeric results and sample sizes further complicates the interpretation of these findings.

Key findings

  • Thymosin α1 did not restore F508del-CFTR function in human airway epithelial cells, n=Not reported in abstract.
  • Not reported in abstract.
  • Not reported in abstract.

Limitations

  • Cellular model only, no human data.
  • Specific numeric results not reported.
  • No details on dose or duration of treatment.

Elsewhere in the Thymosin Alpha-1 corpus

BThymosin α1-induced secretion of the IL-15/RA complex by THP-1-derived dendritic cells restrains HIV latency in vitro.Virulence · 2026 · Intracellular p24 levels in CD4+ T cells decreased significantly, p=0.002.HumanDReply to 'F508del-CFTR is not corrected by thymosin α1'.Nature medicine · 2018AThe efficacy and safety of thymosin α1 for sepsis (TESTS): multicentre, double blinded, randomised, placebo controlled, phase 3 trial.BMJ (Clinical research ed.) · 2025 · 28-day all-cause mortality: 23.4% (127/542) in thymosin α1 group vs 24.1% (132/547) in placebo group, hazard ratio 0.99, 95% CI 0.77 to 1.27, P=0.93.HumanBProximal tubule reabsorptive dysfunction and risk of cardiovascular death among community-living adults: the HUNT-3 cohort.europepmc · 2026 · 1-SD higher urine A1M associated with HR 1.33 (95% CI 1.12-1.58) for cardiovascular death.HumanBPrecision biomarker discovery in hypertension through explainable AI and proteomics.europepmc · 2026 · AUROC = 0.7985 for CatBoost classifier.HumanBExploration and optimization of a respiratory outpatient triage model during the X disease epidemic: A retrospective observational study.europepmc · 2026 · Mean daily patient throughput of 550.43 (SD ± 284.13) individuals.Human