弓形虫的免疫反应——RH:弓形虫免疫反应的最新进展

IF 3 3区 医学 Q3 IMMUNOLOGY
M. Sana, M. Rashid, I. Rashid, H. Akbar, J. Gómez‐Marín, I. Dimier-Poisson
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引用次数: 14

摘要

细胞因子是免疫的可溶性介质,是先天免疫系统和适应性免疫系统的关键因子。它们由各种类型的免疫细胞分泌并与之相互作用,以操纵宿主的免疫细胞生理机能,对抗异物。本研究旨在从宿主免疫反应的角度探讨弓形虫(T.gondii)抵抗的机制。方法和结果宿主(小鼠和人类)对弓形虫免疫反应方面的已发表数据来自Google学者和PubMed。大多数相关文献被纳入本研究。免疫反应的基本机制始于抗原与宿主免疫细胞的相互作用,以触发细胞因子(促炎和抗炎)的产生,然后通过形成细胞因子(细胞因子网络)发挥作用。它们的分泌平衡对于赋予宿主抵抗传染病,特别是弓形虫病的能力至关重要。Th1、Th2和Th17细胞因子之间的狭窄平衡(迄今为止已证明)对于对弓形虫产生耐药性以及宿主的生存至关重要。促炎细胞因子的过量产生会导致组织损伤,从而产生抗炎细胞因子,从而增强弓形虫的增殖。压力和其他传染病(人类免疫缺陷病毒(HIV))削弱了宿主的免疫力,特别是细胞成分,使宿主容易感染弓形虫,尤其是孕妇。结论弓形虫暴露于DCs、Np和MΦ后,体外收获IL12可能是弓形虫病治疗的来源。目前的综述还表明,导致感染宿主上调/补充SOCS-3、IL12和IFNγ的治疗干预措施可能是对抗弓形虫感染的无菌免疫的解决方案。这对因任何原因而经历免疫抑制的患者尤其感兴趣,如接受抗癌治疗的患者、接受移植物/移植免疫抑制治疗的患者,患有免疫缺陷病毒(HIV)或患有艾滋病的患者。另一个重要的建议是启动基于弓形虫GRA6Nt或其他类似抗原的疫苗的研发,作为摧毁组织囊肿的可能工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immune response against toxoplasmosis—some recent updates RH: Toxoplasma gondii immune response
Aims Cytokines, soluble mediators of immunity, are key factors of the innate and adaptive immune system. They are secreted from and interact with various types of immune cells to manipulate host body’s immune cell physiology for a counter-attack on the foreign body. A study was designed to explore the mechanism of Toxoplasma gondii (T. gondii) resistance from host immune response. Methods and results The published data on aspect of host (murine and human) immune response against T. gondii was taken from Google scholar and PubMed. Most relevant literature was included in this study. The basic mechanism of immune response starts from the interactions of antigens with host immune cells to trigger the production of cytokines (pro-inflammatory and anti-inflammatory) which then act by forming a cytokinome (network of cytokine). Their secretory equilibrium is essential for endowing resistance to the host against infectious diseases, particularly toxoplasmosis. A narrow balance lying between Th1, Th2, and Th17 cytokines (as demonstrated until now) is essential for the development of resistance against T. gondii as well as for the survival of host. Excessive production of pro-inflammatory cytokines leads to tissue damage resulting in the production of anti-inflammatory cytokines which enhances the proliferation of Toxoplasma. Stress and other infectious diseases (human immunodeficiency virus (HIV)) that weaken the host immunity particularly the cellular component, make the host susceptible to toxoplasmosis especially in pregnant women. Conclusion The current review findings state that in vitro harvesting of IL12 from DCs, Np and MΦ upon exposure with T. gondii might be a source for therapeutic use in toxoplasmosis. Current review also suggests that therapeutic interventions leading to up-regulation/supplementation of SOCS-3, IL12, and IFNγ to the infected host could be a solution to sterile immunity against T. gondii infection. This would be of interest particularly in patients passing through immunosuppression owing to any reason like the ones receiving anti-cancer therapy, the ones undergoing immunosuppressive therapy for graft/transplantation, the ones suffering from immunodeficiency virus (HIV) or having AIDS. Another imortant suggestion is to launch the efforts for a vaccine based on GRA6Nt or other similar antigens of T. gondii as a probable tool to destroy tissue cysts.
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来源期刊
CiteScore
4.00
自引率
0.00%
发文量
88
审稿时长
15 weeks
期刊介绍: International Journal of Immunopathology and Pharmacology is an Open Access peer-reviewed journal publishing original papers describing research in the fields of immunology, pathology and pharmacology. The intention is that the journal should reflect both the experimental and clinical aspects of immunology as well as advances in the understanding of the pathology and pharmacology of the immune system.
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