A new immunomodulatory therapy for severe sepsis: Ulinastatin Plus Thymosin {alpha} 1.
Chiriva-Internati. M M; Wachtel. M S MS; Frezza. E E EE
Key Findings
- Combined ulinastatin + thymosin‑alpha‑1 raised 28‑day survival from 60% to 78% in sepsis patients
- Leukocyte, lymphocyte counts and coagulation parameters improved more quickly with the combo
- Cytokine levels normalized faster in the treatment group
Practical Outcomes
- The result hints that thymosin‑alpha‑1 may help the immune system during severe infection, but it isn’t a ready‑to‑use supplement for everyday health or performance. Any use should be under medical supervision and is not recommended for healthy self‑experimenters without further evidence.
Summary
A small study gave sepsis patients a combo of two drugs—ulinastatin and thymosin‑alpha‑1—and saw better survival (78% vs 60%) and faster recovery of immune and blood‑clotting markers, but the research was done on very sick hospital patients, not healthy people.
Abstract
To study the effect of immunomodulatory therapy with ulinastatin plus thymosin alpha( 1) on septic patients. A total of 56 sepsis patients were randomized into a treatment group, receiving immunomodulatory therapy, and a placebo group, a placebo. Acute Physiology and Chronic Health Evaluation II scores, clinical data, lymphocyte subsets, immunological indexes, and coagulation parameters were determined before admission and on the 3rd, 8th, and 28th day after admission to the Intensive Care Unit. The treatment group experienced a 78% cumulative survival, the placebo group experienced a 60% cumulative survival; the survival difference was mirrored by Acute Physiology and Chronic Health Evaluation II scores and more quickly improved leukocyte counts, lymphocyte counts, coagulation parameters, and cytokine levels in the treatment. Combined immunomodulatory therapy with ulinastatin plus thymosin alpha(1) appears to yield improved survival for patients with sepsis; this finding should be verified in larger clinical trials.
Study Information
pubmed
2008
2008-11-25T00:00:00.000Z
10.1177/0885066608326970
41
51