AUTHOR=Normile Tyler G. , Del Poeta Maurizio 

TITLE=Three Models of Vaccination Strategies Against Cryptococcosis in Immunocompromised Hosts Using Heat-Killed Cryptococcus neoformans Δsgl1

JOURNAL=Frontiers in Immunology

VOLUME=13

YEAR=2022

URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2022.868523

DOI=10.3389/fimmu.2022.868523

ISSN=1664-3224

ABSTRACT=<p>Vaccines are one of the greatest medical accomplishments to date, yet no fungal vaccines are currently available in humans mainly because opportunistic mycoses generally occur during immunodeficiencies necessary for vaccine protection. In previous studies, a live, attenuated <italic>Cryptococcus neoformans</italic> Δ<italic>sgl1</italic> mutant accumulating sterylglucosides was found to be avirulent and protected mice from a subsequent lethal infection even in absence of CD4<sup>+</sup> T cells, a condition most associated with cryptococcosis (e.g., HIV). Here, we tested three strategies of vaccination against cryptococcosis. First, in our preventative model, protection was achieved even after a 3-fold increase of the vaccination window. Second, because live <italic>C. neoformans</italic> Δ<italic>sgl1</italic>-vaccinated mice challenged more than once with WT strain had a significant decrease in lung fungal burden, we tested <italic>C. neoformans</italic> Δ<italic>sgl1</italic> as an immunotherapeutic. We found that therapeutic administrations of HK <italic>C. neoformans</italic> Δ<italic>sgl1</italic> post WT challenge significantly improves the lung fungal burden. Similarly, therapeutic administration of HK <italic>C. neoformans</italic> Δ<italic>sgl1</italic> post WT challenge resulted in 100% or 70% survival depending on the time of vaccine administration, suggesting that HK Δ<italic>sgl1</italic> is a robust immunotherapeutic option. Third, we investigated a novel model of vaccination in preventing reactivation from lung granuloma using <italic>C. neoformans</italic> Δ<italic>gcs1</italic>. Remarkably, we show that administration of HK Δ<italic>sgl1</italic> prevents mice from reactivating Δ<italic>gcs1</italic> upon inducing immunosuppression with corticosteroids or by depleting CD4<sup>+</sup> T cells. Our results suggest that HK Δ<italic>sgl1</italic> represents a clinically relevant, efficacious vaccine that confers robust host protection in three models of vaccination against cryptococcosis even during CD4-deficiency.</p>