针对新型隐球菌的半合成糖结合疫苗候选物。

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-05-31 DOI:10.1021/acsinfecdis.4c00094
Conor J. Crawford, Livia Liporagi-Lopes, Carolina Coelho, Samuel R. Santos Junior, André Moraes Nicola, Maggie P. Wear, Raghav Vij, Stefan Oscarson* and Arturo Casadevall*, 
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引用次数: 0

摘要

新生隐球菌是一种被世界卫生组织列为极其重要病原体的真菌,对免疫力低下的人构成重大威胁。在本研究中,我们介绍了针对新生隐球菌荚膜多糖葡萄糖醛酸甘露聚糖(GXM)的两种半合成候选疫苗的化学合成和评估。这些半合成糖结合疫苗含有相同的合成十糖(M2 motif)抗原。这种抗原存在于血清型 A 菌株中,占临床隐球菌病病例的 95%。这种合成寡糖与两种蛋白质(CRM197 和炭疽 63 kDa PA)共轭,并在小鼠体内进行了免疫原性试验。这些共轭物引起了与 M2 基团结合的特异性抗体反应,但也表现出了与 M1 和 M4 GXM 基团的交叉反应。在酶联免疫吸附试验和活的真菌细胞中,这两种糖共轭物都能产生与 GXM 结合的抗体。用 CRM197 糖共轭物免疫的小鼠会产生微弱的眼源性抗体,与注射模拟 PBS 的小鼠相比,小鼠的中位存活率呈上升趋势(18 天 vs 15 天,p = 0.06)。这些研究结果表明,要成功制成疫苗,还需要进一步优化糖共轭物。这种抗原可作为多价 GXM 主题疫苗的组成部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Semisynthetic Glycoconjugate Vaccine Candidates against Cryptococcus neoformans

Cryptococcus neoformans is a fungus classified by the World Health Organization as a critically important pathogen, which poses a significant threat to immunocompromised individuals. In this study, we present the chemical synthesis and evaluation of two semisynthetic vaccine candidates targeting the capsular polysaccharide glucuronoxylomannan (GXM) of C. neoformans. These semisynthetic glycoconjugate vaccines contain an identical synthetic decasaccharide (M2 motif) antigen. This antigen is present in serotype A strains, which constitute 95% of the clinical cryptococcosis cases. This synthetic oligosaccharide was conjugated to two proteins (CRM197 and Anthrax 63 kDa PA) and tested for immunogenicity in mice. The conjugates elicited a specific antibody response that bound to the M2 motif but also exhibited additional cross-reactivity toward M1 and M4 GXM motifs. Both glycoconjugates produced antibodies that bound to GXM in ELISA assays and to live fungal cells. Mice immunized with the CRM197 glycoconjugate produced weakly opsonic antibodies and displayed trends toward increased median survival relative to mice given a mock PBS injection (18 vs 15 days, p = 0.06). These findings indicate promise, achieving a successful vaccine demands further optimization of the glycoconjugate. This antigen could serve as a component in a multivalent GXM motif vaccine.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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