Martínez-López Raquel, Molero Gloria, Parra-Giraldo Claudia Marcela, Cabeza Matías Sebastián, Castejón Guillermo, García-Durán Carmen, Clemente Luis Felipe, Hernáez María Luisa, Gil Concha, Monteoliva Lucía
Department of Microbiology and Parasitology, Pharmacy Faculty at Complutense University of Madrid, 28040 Madrid, Spain.
Mycology and Molecular Diagnostics Laboratory, Biochemistry and Biological Science Faculty, Nacional del Litoral University, Santa Fe 3000, Argentina.
Int J Mol Sci. 2024 Dec 30;26(1):244. doi: 10.3390/ijms26010244.
Extracellular vesicles (EVs) from can elicit immune responses, positioning them as promising acellular vaccine candidates. We characterized EVs from an avirulent cell wall mutant (Δ) and evaluated their protective potential against invasive candidiasis. EVs from the yeast (YEVs) and hyphal (HEVs) forms of the SC5314 wild-type strain were also tested, yielding high survival rates with SC5314 YEV (91%) and YEV immunization (64%). Surprisingly, HEV immunization showed a dual effect, resulting in 36% protection but also causing premature death in some mice. Proteomic analyses revealed distinct profiles among the top 100 proteins in the different EVs, which may explain these effects: a shared core of 50 immunogenic proteins such as Pgk1, Cdc19, and Fba1; unique, relevant immunogenic proteins in SC5314 YEVs; and proteins linked to pathogenesis, like Ece1 in SC5314 HEVs. Sera from SC5314 YEV-immunized mice showed the highest IgG2a titers and moderate IL-17, IFN-γ, and TNF-α levels, indicating the importance of both humoral and cellular responses for protection. These findings highlight the distinct immunogenic properties of EVs, suggesting their potential in acellular vaccine development while emphasizing the need to carefully evaluate pathogenic risks associated with certain EVs.
来自[具体菌株名称未给出]的细胞外囊泡(EVs)可引发免疫反应,使其成为有前景的无细胞疫苗候选物。我们对无毒力的[具体菌株名称未给出]细胞壁突变体(Δ)的EVs进行了表征,并评估了它们对侵袭性念珠菌病的保护潜力。还测试了SC5314野生型菌株酵母形式(YEVs)和菌丝形式(HEVs)的EVs,SC5314 YEV免疫(91%)和[具体菌株名称未给出]YEV免疫(64%)的小鼠存活率较高。令人惊讶的是,HEV免疫显示出双重作用,导致36%的保护率,但也导致一些小鼠过早死亡。蛋白质组学分析揭示了不同EVs中前100种蛋白质的不同概况,这可能解释了这些作用:50种免疫原性蛋白质的共同核心,如Pgk1、Cdc19和Fba1;SC5314 YEVs中独特的、相关的免疫原性蛋白质;以及与发病机制相关的蛋白质,如SC5314 HEVs中的Ece1。来自SC5314 YEV免疫小鼠的血清显示出最高的IgG2a滴度以及中等水平的IL-17、IFN-γ和TNF-α,表明体液和细胞反应对保护都很重要。这些发现突出了[具体菌株名称未给出]EVs独特的免疫原性特性,表明它们在无细胞疫苗开发中的潜力,同时强调需要仔细评估与某些EVs相关的致病风险。