Barros Mariana, Teixeira Daniela, Vilanova Manuel, Correia Alexandra, Teixeira Natercia, Borges Margarida
Departamento de Ciências Biológicas, Faculdade de Farmácia, Universidade do Porto, Porto, Portugal.
Immunobiology Group, Instituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto, Porto, Portugal.
Front Immunol. 2021 Feb 15;11:621997. doi: 10.3389/fimmu.2020.621997. eCollection 2020.
Congenital toxoplasmosis has a high impact on human disease worldwide, inducing serious consequences from fetus to adulthood. Despite this, there are currently no human vaccines available to prevent this infection. Most vaccination studies against infection used animal models in which the infection was established by exogenous inoculation. Here, we review recent research on potential vaccines using animal models in which infection was congenitally established. Endeavors in this field have so far revealed that live or subunit vaccines previously found to confer protection against extrinsically established infections can also protect, at least partially, from vertically transmitted infection. Nevertheless, there is no consensus on the more adequate immune response to protect the host and the fetus in congenital infection. Most of the vaccination studies rely on the assessment of maternal systemic immune responses, quantification of parasitic loads in the fetuses, and survival indexes and/or brain parasitic burden in the neonates. More research must be carried out not only to explore new vaccines but also to further study the nature of the elicited immune protection at the maternal-fetal interface. Particularly, the cellular and molecular effector mechanisms at the maternal-fetal interface induced by immunization remain poorly characterized. Deeper knowledge on the immune response at this specific location will certainly help to refine the vaccine-induced immunity and, consequently, to provide the most effective and safest protection against vertical infection.
先天性弓形虫病在全球范围内对人类疾病有重大影响,可导致从胎儿期到成年期的严重后果。尽管如此,目前尚无预防这种感染的人类疫苗。大多数针对该感染的疫苗研究使用的动物模型是通过外源性接种建立感染的。在此,我们综述了近期使用先天性建立感染的动物模型进行潜在疫苗研究的情况。该领域的研究迄今表明,先前发现能对外部建立的感染提供保护的活疫苗或亚单位疫苗,也能至少部分地保护免受垂直传播感染。然而,对于在先天性感染中保护宿主和胎儿的更合适免疫反应尚无共识。大多数疫苗研究依赖于评估母体的全身免疫反应、量化胎儿体内的寄生虫负荷以及新生儿的生存指数和/或脑内寄生虫负担。不仅要开展更多研究以探索新疫苗,还需进一步研究在母胎界面引发的免疫保护的性质。特别是,免疫接种在母胎界面诱导的细胞和分子效应机制仍不清楚。深入了解这一特定部位的免疫反应肯定有助于优化疫苗诱导的免疫,从而提供针对垂直感染的最有效和最安全保护。