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Semisynthetic Glycoconjugate Vaccine Candidates against <i>Cryptococcus neoformans</i>

C. Crawford, Livia Liporagi-Lopes, Carolina Coelho, Samuel Ricardo dos Santos, André Moraes Nicola, Maggie P. Wear, Raghav Vij, Stefan Oscarson, Arturo Casadevall

2024ACS Infectious Diseases13 citationsDOIOpen Access PDF

Abstract

High Resolution Image Download MS PowerPoint Slide 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.

Topics & Concepts

Cryptococcus neoformansGlycoconjugateMicrobiologyBiologyCryptococcusVirologyCryptococcosisMedicineImmunologyBioinformaticsFungal Infections and StudiesAntifungal resistance and susceptibilityToxin Mechanisms and Immunotoxins