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抗隐球菌病的有前景的全细胞疫苗。

Promising whole-cell vaccines against cryptococcosis.

机构信息

Department of Fungal Infection, National Institute of Infectious Diseases, Tokyo, Japan.

Department of Biological Science and Technology, Faculty of Industrial Science and Technology, Tokyo University of Science, Tokyo, Japan.

出版信息

Microbiol Immunol. 2023 May;67(5):211-223. doi: 10.1111/1348-0421.13056. Epub 2023 Mar 5.

Abstract

Cryptococcosis is a mycosis caused by Cryptococcus neoformans and C. gattii species complexes. Although this infection is potentially lethal, no prophylactic vaccine is yet commercially available, and the immune memory that enables prevention is still under investigation. These pathogens have a capsule layer for immune evasion and a sophisticated mechanism to advance the infection, and it is expected that these characteristics will make it difficult to develop prophylactic vaccines and to decipher the protective immunity. The current vaccine studies are focused on subunit, mRNA, DNA, and viral vector vaccines, with whole-cell vaccines also proving successful against cryptococcal infections. Cryptococcal whole-cell vaccines have been composed of highly immunostimulating strains with low-pathogenicity that are modified by genetic recombination technology. Examples include the whole-cell vaccines H99γ, sgl1∆, fbp1∆, znf2 , cda1/2/3∆, cap59∆, and cap60∆. Some of these whole-cell vaccines were found to be highly effective in prolonging life and suppressing the fungal burden after an infection challenge in mice, and to be cross-reactive to C. neoformans, C. gattii, and other fungal pathogens. Furthermore, for some vaccines, the protective effect can be retained even in an immunocompromised host depleted of CD4 T cells. These findings have provided new insights into protective immunity that should aid in vaccine development. In this review, we highlight the upsides and downsides of whole-cell vaccines against cryptococcosis.

摘要

隐球菌病是由新生隐球菌和格特隐球菌复合体引起的真菌感染。尽管这种感染具有潜在的致命性,但目前尚无商业可用的预防性疫苗,而能够预防感染的免疫记忆仍在研究中。这些病原体具有用于免疫逃避的胶囊层和推进感染的复杂机制,预计这些特征将使预防性疫苗的开发和保护性免疫的破译变得困难。目前的疫苗研究集中在亚单位、mRNA、DNA 和病毒载体疫苗上,全细胞疫苗也被证明对隐球菌感染有效。隐球菌全细胞疫苗由高度免疫刺激的低致病性菌株组成,这些菌株经过基因重组技术进行修饰。例如,H99γ、sgl1∆、fbp1∆、znf2、cda1/2/3∆、cap59∆和 cap60∆等全细胞疫苗。这些全细胞疫苗中的一些在延长生命和抑制小鼠感染后真菌负荷方面表现出高度有效性,并对新生隐球菌、格特隐球菌和其他真菌病原体具有交叉反应性。此外,对于一些疫苗,即使在耗尽 CD4 T 细胞的免疫功能低下的宿主中,保护作用也能保留。这些发现为保护性免疫提供了新的见解,应该有助于疫苗的开发。在这篇综述中,我们强调了针对隐球菌病的全细胞疫苗的优缺点。

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