Immunoregulation of thymosin alpha 1 treatment of cytomegalovirus infection accompanied with acute respiratory distress syndrome after renal transplantation.
Ji. S-M SM; Li. L-S LS; Sun. Q-Q QQ; Chen. J-S JS; Sha. G-Z GZ; Liu. Z-H ZH
Key Findings
- Rescue success rose from 50% to 78% with thymosin‑alpha‑1
- Death rate fell from 50% to about 22% in the treated group
- CD4+ T‑cells and the CD4/CD8 ratio increased significantly after 2 weeks
Practical Outcomes
- Thymosin‑alpha‑1 may act as an immune‑boosting agent, especially for people with very weak immunity, but the evidence is limited to sick transplant patients. The studied dose was 1.6 mg subcutaneously every other day or daily, and it should only be used under medical supervision due to the serious context of the trial.
Summary
In a small study of kidney‑transplant patients who got a serious CMV infection and lung trouble, adding the peptide thymosin‑alpha‑1 (1.6 mg under the skin every 1‑2 days) helped more people survive and boosted their key immune cells (CD4 and CD8 T‑cells).
Abstract
We are the first to report the use of thymosin alpha1 to treat cytomegalovirus infection accompanied with acute respiratory distress syndrome after renal transplantation. The patients were divided into the thymosin alpha1 group (Zadaxin group, n = 32) and the control group (n = 14). All patients received the same rescue therapy protocol. Suitable antiviral (ganciclovir, 5 mg/kg every 12 hours, intravenously), antibacterial, or antifungal treatment was given if needed. In addition, patients in the Zadaxin group received thymosin alpha1, (1.6 mg) subcutaneously every other day or every day. The rescue success rate was significantly higher in the Zadaxin than in the control group (78.1% vs 50.0%) while the death rate was greatly reduced (21.9% vs 50%). In the Zadaxin group, the CD4(+) lymphocyte level was significantly increased on day 14; so was the ratio of CD4(+) and CD8(+) T-lymphocyte subsets. In the survival group, CD4(+) and CD8(+) lymphocyte cell counts were significantly increased on days 7, 14, and 21 compared with admission. This study suggested that thymosin alpha1 significantly promoted CD4(+) and CD8(+) lymphocytes, repairing cellular immunity and successfully reinforcing resistance to cytomegalovirus disease.
Study Information
pubmed
2007
10.1016/j.transproceed.2006.10.005