Department of Biochemistry and Immunology, Institute of Biological Science, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Department of Biochemistry and Immunology, Institute of Biological Science, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil; ISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Clin Immunol. 2021 May;226:108713. doi: 10.1016/j.clim.2021.108713. Epub 2021 Mar 9.
Current chemical therapies for Chagas Disease (CD) lack ability to clear Trypanosoma cruzi (Tc) parasites and cause severe side effects, making search for new strategies extremely necessary. We evaluated the action of Tityus serrulatus venom (TsV) components during Tc infection. TsV treatment increased nitric oxide and pro-inflammatory cytokine production by Tc-infected macrophages (MØ), decreased intracellular parasite replication and trypomastigotes release, also triggering ERK1/2, JNK1/2 and p38 activation. Ts7 demonstrated the highest anti-Tc activity, inducing high levels of TNF and IL-6 in infected MØ. TsV/Ts7 presented synergistic effect on p38 activation when incubated with Tc antigen. KPP-treatment of MØ also decreased trypomastigotes releasing, partially due to p38 activation. TsV/Ts7-pre-incubation of Tc demonstrated a direct effect on parasite decreasing MØ-trypomastigotes releasing. In vivo KPP-treatment of Tc-infected mice resulted in decreased parasitemia. Summarizing, this study opens perspectives for new bioactive molecules as CD-therapeutic treatment, demonstrating the TsV/Ts7/KPP-trypanocidal and immunomodulatory activity during Tc infection.
目前用于恰加斯病(CD)的化学疗法缺乏清除克氏锥虫(Tc)寄生虫的能力,并会导致严重的副作用,因此极有必要寻找新的策略。我们评估了蒂图蛛属毒液(TsV)成分在 Tc 感染期间的作用。TsV 治疗可增加 Tc 感染的巨噬细胞(MØ)中一氧化氮和促炎细胞因子的产生,减少细胞内寄生虫复制和游离锥虫的释放,还可触发 ERK1/2、JNK1/2 和 p38 的激活。Ts7 对 Tc 表现出最高的抗活性,可诱导感染的 MØ 中 TNF 和 IL-6 的高水平产生。TsV/Ts7 与 Tc 抗原孵育时,对 p38 激活表现出协同作用。KPP 处理 MØ 也可减少游离锥虫的释放,部分原因是 p38 的激活。TsV/Ts7 预处理 Tc 可直接减少寄生虫释放,从而减少 MØ 释放游离锥虫。体内 KPP 处理 Tc 感染的小鼠可降低寄生虫血症。综上所述,该研究为新型生物活性分子作为 CD 治疗方法提供了前景,证明了 TsV/Ts7/KPP 在 Tc 感染期间具有抗寄生虫和免疫调节活性。