Recent Advances in the Development of Adenovirus-Vectored Vaccines for Parasitic Infections.

Pharmaceuticals (Basel)

Division of Experimental Medicine, McGill University, Montreal, QC H3A 3J1, Canada.

Published: February 2023

AI Article Synopsis

  • Vaccines for parasitic diseases have fallen significantly behind those for viral and bacterial infections, even though these diseases have severe health impacts worldwide.
  • One major challenge in developing effective parasite vaccines is the need for complex immune responses that can fight against parasitic persistence.
  • Adenovirus vectors are emerging as a promising solution, showing potential in eliciting strong immune responses that could lead to effective vaccines for several key parasitic diseases like malaria, Chagas disease, and schistosomiasis.

Article Abstract

Vaccines against parasites have lagged centuries behind those against viral and bacterial infections, despite the devastating morbidity and widespread effects of parasitic diseases across the globe. One of the greatest hurdles to parasite vaccine development has been the lack of vaccine strategies able to elicit the complex and multifaceted immune responses needed to abrogate parasitic persistence. Viral vectors, especially adenovirus (AdV) vectors, have emerged as a potential solution for complex disease targets, including HIV, tuberculosis, and parasitic diseases, to name a few. AdVs are highly immunogenic and are uniquely able to drive CD8+ T cell responses, which are known to be correlates of immunity in infections with most protozoan and some helminthic parasites. This review presents recent developments in AdV-vectored vaccines targeting five major human parasitic diseases: malaria, Chagas disease, schistosomiasis, leishmaniasis, and toxoplasmosis. Many AdV-vectored vaccines have been developed for these diseases, utilizing a wide variety of vectors, antigens, and modes of delivery. AdV-vectored vaccines are a promising approach for the historically challenging target of human parasitic diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10058461PMC
http://dx.doi.org/10.3390/ph16030334DOI Listing

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