TY - JOUR
T1 - Semisynthetic Glycoconjugate Vaccine Candidates against Cryptococcus neoformans
AU - Crawford, Conor J.
AU - Liporagi-Lopes, Livia
AU - Coelho, Carolina
AU - Santos Junior, Samuel R.
AU - Moraes Nicola, André
AU - Wear, Maggie P.
AU - Vij, Raghav
AU - Oscarson, Stefan
AU - Casadevall, Arturo
N1 - Publisher Copyright:
© 2024 The Authors. Published by American Chemical Society
PY - 2024/6/14
Y1 - 2024/6/14
N2 - 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.
AB - 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.
KW - Cryptococcus neoformans
KW - World Health Organization
KW - clinical cryptococcosis
KW - glucuronoxylomannan (GXM)
KW - glycoconjugates produced
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U2 - 10.1021/acsinfecdis.4c00094
DO - 10.1021/acsinfecdis.4c00094
M3 - Article
C2 - 38819951
AN - SCOPUS:85194944440
SN - 2373-8227
VL - 10
SP - 2089
EP - 2100
JO - ACS Infectious Diseases
JF - ACS Infectious Diseases
IS - 6
ER -