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Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Score 2
2021 pubmed 17 citations

Thymosin Alpha-1 Has no Beneficial Effect on Restoring CD4+ and CD8+ T Lymphocyte Counts in COVID-19 Patients.

Wang. Zhenyan Z; Chen. Jun J; Zhu. Cuiyun C; Liu. Li L; Qi. Tangkai T; Shen. Yinzhong Y; Zhang. Yuyi Y; Xu. Lie L; Li. Tao T; Qian. Zhiping Z; Steinhart. Corklin R CR; Lu. Hongzhou H

Key Findings

  • Thymosin‑alpha‑1 did not increase CD4+ or CD8+ T‑cell counts during recovery.
  • Patients receiving thymosin‑alpha‑1 cleared the virus more slowly than those who did not.
  • Severity of illness and thymosin‑alpha‑1 therapy were linked to longer virus clearance times.

Practical Outcomes

  • For self‑experimenters, thymosin‑alpha‑1 appears to offer no benefit for COVID‑19 immune recovery and may even delay virus clearance. It’s not recommended to add this peptide to a COVID‑19 protocol for boosting T‑cell counts or speeding up recovery.

Summary

A study of 275 COVID‑19 patients found that giving thymosin‑alpha‑1 did not boost the drop in CD4+ or CD8+ T‑cells and actually made the virus take longer to clear, suggesting it isn’t helpful for COVID‑19 recovery.

Abstract

Dysregulation of immune response was observed in COVID-19 patients. Thymosin alpha 1 (T&#x3b1;1) is used in the management of COVID-19, because it is known to restore the homeostasis of the immune system during infections and cancers. We aim to observe the longitudinal changes in T lymphocyte subsets and to evaluate the efficacy of T&#x3b1;1 for COVID-19. A retrospective study was conducted in 275 COVID-19 patients admitted to Shanghai public health clinical center. The clinical and laboratory characteristics between patients with different T lymphocyte phenotypes and those who were and were not treated with T&#x3b1;1 were compared. Among the 275 patients, 137 (49.8%) were males, and the median age was 51 years [interquartile range (IQR): 37-64]. A total of 126 patients received T&#x3b1;1 therapy and 149 patients did not. There were 158 (57.5%) patients with normal baseline CD4 counts (median:631/&#x3bc;L, IQR: 501~762) and 117 patients (42.5%) with decreased baseline CD4 counts (median:271/&#x3bc;L, IQR: 201~335). In those with decreased baseline CD4 counts, more patients were older (p&lt;0.001), presented as critically ill (p=0.032) and had hypertension (p=0.008) compared with those with normal CD4 counts. There was no statistical difference in the duration of virus shedding in the upper respiratory tract between the two groups (p=0.214). In both the normal (14 <i>vs</i> 11, p=0.028) and the decreased baseline CD4 counts group (15 <i>vs</i> 11, p=0.008), duration of virus clearance in the patients with T&#x3b1;1 therapy was significantly longer than that in those without T&#x3b1;1 therapy. There was no significant difference in the increase of CD4+ (286 <i>vs</i> 326, p=0.851) and CD8+ T cell (154 <i>vs</i> 170, p=0.842) counts in the recovery period between the two groups with or without T&#x3b1;1 therapy. Multivariate linear regression analysis showed that severity of illness (p&lt;0.001) and T&#x3b1;1 therapy (p=0.001) were associated with virus clearance. In conclusion, reduction of CD4+ T and CD8+ T cell counts were observed in COVID-19 patients. T&#x3b1;1 may have no benefit on restoring CD4+ and CD8+ T cell counts or on the virus clearance. The use of T&#x3b1;1 for COVID-19 need to be more fully investigated.

Study Information

Provider

pubmed

Year

2021

Date

2021-06-03T00:00:00.000Z

DOI

10.3389/fimmu.2021.568789

Citations

17

References

34