Thymosin Alpha 1 Mitigates Cytokine Storm in Blood Cells From Coronavirus Disease 2019 Patients.
Matteucci. Claudia C; Minutolo. Antonella A; Balestrieri. Emanuela E; Petrone. Vita V; Fanelli. Marialaura M; Malagnino. Vincenzo V; Ianetta. Marco M; Giovinazzo. Alessandro A; Barreca. Filippo F; Di Cesare. Silvia S; De Marco. Patrizia P; Miele. Martino Tony MT; Toschi. Nicola N; Mastino. Antonio A; Sinibaldi Vallebona. Paola P; Bernardini. Sergio S; Rogliani. Paola P; Sarmati. Loredana L; Andreoni. Massimo M; Grelli. Sandro S; Garaci. Enrico E
Key Findings
- COVID‑19 blood cells show high levels of cytokine‑related genes.
- Ex\xa0vivo treatment with thymosin‑alpha‑1 reduced cytokine gene expression.
- The peptide specifically dampened activation of a CD8+ T‑cell subset.
Practical Outcomes
- For self‑directed health optimizers, thymosin‑alpha‑1 appears to have immune‑modulating properties that could be useful in managing severe viral inflammation, but the study provides no dosing guidance or real‑world protocol. Until more clinical data are available, it remains a promising but experimental tool rather than a ready‑to‑use supplement.
Summary
A study showed that the peptide thymosin‑alpha‑1 can calm down the overactive immune response seen in COVID‑19 patients by lowering cytokine production and slowing certain T‑cell activity when tested on blood cells outside the body. This suggests it might help keep the immune system balanced during severe infections.
Abstract
Coronavirus disease 2019 (COVID-19) is characterized by immune-mediated lung injury and complex alterations of the immune system, such as lymphopenia and cytokine storm, that have been associated with adverse outcomes underlining a fundamental role of host response in severe acute respiratory syndrome coronavirus 2 infection and the pathogenesis of the disease. Thymosin alpha 1 (Tα1) is one of the molecules used in the management of COVID-19, because it is known to restore the homeostasis of the immune system during infections and cancer. In this study, we captured the interconnected biological processes regulated by Tα1 in CD8+ T cells under inflammatory conditions. Genes associated with cytokine signaling and production were upregulated in blood cells from patients with COVID-19, and the ex vivo treatment with Tα1-mitigated cytokine expression, and inhibited lymphocyte activation in a CD8+ T-cell subset specifically. These data suggest the potential role of Tα1 in modulating the immune response homeostasis and the cytokine storm in vivo.
Study Information
pubmed
2020
2020-12-05T00:00:00.000Z
10.1093/ofid/ofaa588
35
55