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Role of γδ T cells in controlling viral infections with a focus on influenza virus: implications for designing novel therapeutic approaches

机译:γδT细胞对病毒感染控制病毒感染的作用:用于设计新型治疗方法的含义

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Influenza virus infection is among the most detrimental threats to the health of humans and some animals, infecting millions of people annually all around the world and in many thousands of cases giving rise to pneumonia and death. All those health crises happen despite previous and recent developments in anti-influenza vaccination, suggesting the need for employing more sophisticated methods to control this malign infection. Main body The innate immunity modules are at the forefront of combating against influenza infection in the respiratory tract, among which, innate T cells, particularly gamma-delta (γδ) T cells, play a critical role in filling the gap needed for adaptive immune cells maturation, linking the innate and adaptive immunity together. Upon infection with influenza virus, production of cytokines and chemokines including CCL3, CCL4, and CCL5 from respiratory epithelium recruits γδ T cells at the site of infection in a CCR5 receptor-dependent fashion. Next, γδ T cells become activated in response to influenza virus infection and produce large amounts of proinflammatory cytokines, especially IL-17A. Regardless of γδ T cells’ roles in triggering the adaptive arm of the immune system, they also protect the respiratory epithelium by cytolytic and non-cytolytic antiviral mechanisms, as well as by enhancing neutrophils and natural killer cells recruitment to the infection site. In this review, we explored varied strategies of γδ T cells in defense to influenza virus infection and how they can potentially provide balanced protective immune responses against infected cells. The results may provide a potential window for the incorporation of intact or engineered γδ T cells for developing novel antiviral approaches or for immunotherapeutic purposes.
机译:流感病毒感染是对人类和一些动物健康的最不利威胁之一,每年都在世界各地感染数百万人,并且在数千个病例中引起肺炎和死亡。尽管抗流感疫苗接种的先前和最近的发展,所有这些健康危机都会发生,这表明需要采用更复杂的方法来控制这种恶性感染。主体是先天免疫模块处于对抗呼吸道中的流感感染的最前沿,其中,先天T细胞,特别是γ-δ(γδ)T细胞,在填充适应性免疫细胞所需的间隙方面发挥着关键作用成熟,将先天和自适应免疫连接在一起。对流感病毒感染,细胞因子和趋化因子,包括CCL3,CCL4和CCL5的来自呼吸上皮,以CCR5受体依赖性方式促进感染部位的γδT细胞。接下来,γδT细胞响应流感病毒感染而激活,并产生大量的促炎细胞因子,特别是IL-17a。无论γδT细胞的角色如何触发免疫系统的自适应臂,它们也通过细胞溶解和非细胞溶解抗病毒机制保护呼吸上皮,以及通过增强中性粒细胞和天然杀手细胞募集到感染部位。在本综述中,我们探讨了对流感病毒感染的γδT细胞的各种策略以及它们如何潜在地提供针对感染细胞的平衡保护性免疫应答。结果可以提供用于掺入完整或工程化γδT细胞的潜在窗口,以发展新的抗病毒方法或用于免疫治疗目的。

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