Department of Parasitology, 66920University of Veterinary and Animal Sciences, Lahore, Pakistan.
Department of Parasitology, Faculty of Veterinary and Animal Sciences, 66920The Islamia University of Bahawalpur, Pakistan.
Int J Immunopathol Pharmacol. 2022 Jan-Dec;36:3946320221078436. doi: 10.1177/03946320221078436.
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 () resistance from host immune response.
The published data on aspect of host (murine and human) immune response against 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 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 . 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.
The current review findings state that harvesting of IL12 from DCs, Np and MΦ upon exposure with 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 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 as a probable tool to destroy tissue cysts.
细胞因子是免疫的可溶性介质,是先天和适应性免疫系统的关键因素。它们由各种免疫细胞分泌并相互作用,以操纵宿主的免疫细胞生理学,从而对异物发起反击。本研究旨在探讨宿主免疫反应对()产生抗性的机制。
从 Google Scholar 和 PubMed 上获取了关于宿主(鼠和人)对的免疫反应的已发表数据。本研究纳入了大多数相关文献。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,触发细胞因子(促炎和抗炎)的产生,然后通过形成细胞因子组(细胞因子网络)发挥作用。它们的分泌平衡对于赋予宿主对传染病(特别是弓形虫病)的抵抗力至关重要。迄今为止,Th1、Th2 和 Th17 细胞因子之间的狭窄平衡对于抵抗的发展以及宿主的生存至关重要。促炎细胞因子的过度产生导致组织损伤,从而产生抗炎细胞因子,促进的增殖。压力和其他传染病(人类免疫缺陷病毒(HIV))会削弱宿主的免疫力,特别是细胞成分,使宿主易患弓形虫病,尤其是孕妇。
本综述的研究结果表明,从暴露于弓形虫的 DCs、Np 和 MΦ 中提取 IL12 可能成为弓形虫病治疗的一种来源。本综述还表明,导致 SOCS-3、IL12 和 IFNγ 的上调/补充到感染宿主的治疗干预可能是针对感染产生无菌免疫的一种解决方案。这对于因任何原因接受抗癌治疗、因移植而接受免疫抑制治疗、感染人类免疫缺陷病毒(HIV)或患有艾滋病的患者尤其感兴趣。另一个重要的建议是努力开发基于 GRA6Nt 或其他类似弓形虫抗原的疫苗,作为破坏组织囊肿的可能工具。