Centre for Synthesis and Chemical Biology, University College Dublin, Belfield, Dublin D04 V1W8, Ireland.
Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, 615 North Wolfe Street, Baltimore 21205, Maryland, United States.
ACS Infect Dis. 2024 Jun 14;10(6):2089-2100. doi: 10.1021/acsinfecdis.4c00094. Epub 2024 May 31.
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 . 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, = 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.
荚膜组织胞浆菌被世界卫生组织归类为一种极重要的病原体,对免疫功能低下的个体构成重大威胁。在这项研究中,我们提出了两种针对荚膜多糖葡聚糖(GXM)的半合成疫苗候选物的化学合成和评估。这些半合成糖缀合物疫苗含有相同的合成十聚糖(M2 基序)抗原。该抗原存在于血清型 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(CRM197 和炭疽 63 kDa PA)缀合,并在小鼠中进行了免疫原性测试。缀合物引起了针对 M2 基序的特异性抗体反应,但也表现出对 M1 和 M4 GXM 基序的额外交叉反应性。两种糖缀合物都产生了与 ELISA 检测中的 GXM 结合的抗体,以及与活真菌细胞结合的抗体。用 CRM197 糖缀合物免疫的小鼠产生了弱的调理抗体,并显示出相对于给予模拟 PBS 注射的小鼠(18 天 vs 15 天, = 0.06)的中位生存期延长趋势。这些发现表明有希望,但要实现成功的疫苗,还需要对半合成糖缀合物进一步优化。该抗原可以作为多价 GXM 基序疫苗的一个组成部分。