Laboratoire d'Epidémiologie et d'Ecologie Parasitaire/Laboratoire d'Epidémiologie Moléculaire et de Pathologie Expérimentale Appliquée (LR11IPT04), Institut Pasteur de Tunis-Université Tunis El Manar, Tunis-Belvédère, Tunisia.
Parasite Immunol. 2013 May-Jun;35(5-6):194-9. doi: 10.1111/pim.12026.
Previously we showed that His-tagged, recombinant, Leishmania infantum eukaryotic initiation factor (LeIF) was both an RNA-dependent ATPase and an ATP-dependent RNA helicase in vitro, as described for other members of the DEAD-box helicase family. In addition, we showed that LeIF induces the production of IL-12, IL-10, and TNF-α by human monocytes. This study aims to characterize the cytokine-inducing activity in human monocytes of several proteins belonging to the DEAD-box family from mammals and yeast. All tested proteins contained the 11 conserved motifs (Q, I, Ia, GG Ib, II, III, IV, QxxR, V and VI) characteristic of DEAD-box proteins, but they have different biological functions and different percentages of identities with LeIF. We show that these mammalian or yeast recombinant proteins also are able to induce IL-12, IL-10 and TNF-α secretion by monocytes of healthy human subjects. This cytokine-inducing activity is proteinase K sensitive and polymyxin B resistant. Our results show that the induction of cytokines in human monocytes is not unique to the protein LeIF of Leishmania, and it suggests that the activity of certain DEAD-box proteins can be exploited as adjuvant and/or to direct immune responses towards a Th1 profile in vaccination or immunotherapy protocols.
先前我们表明,重组的、带有 His 标签的利什曼原虫真核起始因子(LeIF)在体外既是 RNA 依赖性 ATP 酶,也是 ATP 依赖性 RNA 解旋酶,这与 DEAD 盒解旋酶家族的其他成员相同。此外,我们还表明 LeIF 可诱导人单核细胞产生 IL-12、IL-10 和 TNF-α。本研究旨在表征哺乳动物和酵母的 DEAD 盒家族中的几种蛋白在人单核细胞中的细胞因子诱导活性。所有测试的蛋白均含有 DEAD 盒蛋白的 11 个保守基序(Q、I、Ia、GG Ib、II、III、IV、QxxR、V 和 VI),但它们具有不同的生物学功能,与 LeIF 的同源性也不同。我们表明,这些哺乳动物或酵母重组蛋白也能够诱导健康人类受试者单核细胞分泌 IL-12、IL-10 和 TNF-α。这种细胞因子诱导活性对蛋白酶 K敏感,而对多粘菌素 B 有抗性。我们的结果表明,细胞因子在人单核细胞中的诱导并非利什曼原虫蛋白 LeIF 所特有,这表明某些 DEAD 盒蛋白的活性可被用作佐剂和/或在疫苗接种或免疫治疗方案中引导免疫反应朝向 Th1 表型。