Changes of TLR2, TLR4 and MyD88 mRNA expressions on peripheral blood mononuclear cell in severe sepsis patients during treatment with Thymosin α1
Jianfeng Wu, Zhaoxia Tang, Juan Chen, Bin Ouyang, Minying Chen
Abstract
Jianfeng Wu, Zhaoxia Tang, Juan Chen, Bin Ouyang, Minying Chen
Abstract
Objective To examine the TLR2, TLR4 and MyD88 mRNA expressions on human peripheral blood mononuclear cells during treatment. Methods A prospective randomized controlled trial was designed. Fifty-four patients with severe sepsis were enrolled and randomized into thymosin group (26 cases, treated with thymosin alpha 1) and control group (28 cases). TLR2, TLR4 and MyD88 mRNA were tested by RT-PCR on the day of enrollment, day 3 and day 7 after treatment in both groups, 28-day mortality in these patients was analyzed. Results There was no statistically significant difference between 28-day mortality rate in the control group and that of thymosin group (35.7% vs 23.1%, P=0.310). TLR2, TLR4 and MyD88 mRNA expressions in the thymosin group were respectively increased on enrollment day, day 3 and day 7, while this increasing trend was not found in the control group. On day 3, TLR2 and TLR4 mRNA expressions in the thymosin group were higher than those in the control group (2.31±0.79 vs 1.83±0.51, 7.31±0.79 vs 6.55±0.92, P<0.05). On day 7, TLR2, TLR4 and MyD88 mRNA expressions in the thymosin group were higher than those in the control group (2.75±1.17 vs 1.63±0.36, 7.75±1.03 vs 6.39±0.72, 4.26±0.77 vs 3.77±0.68, P<0.05). Conclusion Thymosin alpha 1 may increase TLR2, TLR4 and MyD88 mRNA expressions in severe sepsis patients. Key words: Sepsis; Thymosin alpha 1; Toll like receptor; Myeloid differentiation factor 88
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Objective To examine the TLR2, TLR4 and MyD88 mRNA expressions on human peripheral blood mononuclear cells during treatment. Methods A prospective randomized controlled trial was designed. Fifty-four patients with severe sepsis were enrolled and randomized into thymosin group (26 cases, treated with thymosin alpha 1) and control group (28 cases). TLR2, TLR4 and MyD88 mRNA were tested by RT-PCR on the day of enrollment, day 3 and day 7 after treatment in both groups, 28-day mortality in these patients was analyzed. Results There was no statistically significant difference between 28-day mortality rate in the control group and that of thymosin group (35.7% vs 23.1%, P=0.310). TLR2, TLR4 and MyD88 mRNA expressions in the thymosin group were respectively increased on enrollment day, day 3 and day 7, while this increasing trend was not found in the control group. On day 3, TLR2 and TLR4 mRNA expressions in the thymosin group were higher than those in the control group (2.31±0.79 vs 1.83±0.51, 7.31±0.79 vs 6.55±0.92, P<0.05). On day 7, TLR2, TLR4 and MyD88 mRNA expressions in the thymosin group were higher than those in the control group (2.75±1.17 vs 1.63±0.36, 7.75±1.03 vs 6.39±0.72, 4.26±0.77 vs 3.77±0.68, P<0.05). Conclusion Thymosin alpha 1 may increase TLR2, TLR4 and MyD88 mRNA expressions in severe sepsis patients. Key words: Sepsis; Thymosin alpha 1; Toll like receptor; Myeloid differentiation factor 88
Key concepts: Thymosin, TLR2, Peripheral blood mononuclear cell, TLR4, Sepsis, Medicine, Internal medicine, Messenger RNA