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Drug-cured experimental Trypanosoma cruzi infections confer long-lasting and cross-strain protection.

Gurdip Singh MannAmanda F FranciscoShiromani JayawardhanaMartin C TaylorMichael D LewisFrancisco OlmoElisangela Oliveira de FreitasFabiana M S LeorattiCesar López-CamachoArturo Reyes-SandovalJohn M Kelly
Published in: PLoS neglected tropical diseases (2020)
Our findings suggest that a protective Chagas disease vaccine must have the ability to eliminate parasites before they reach organs/tissues, such as the GI tract, where once established, they become largely refractory to the induced immune response.
Keyphrases
  • trypanosoma cruzi
  • immune response
  • high glucose
  • drug induced
  • diabetic rats
  • gene expression
  • toll like receptor
  • endothelial cells
  • emergency department
  • plasmodium falciparum
  • adverse drug
  • inflammatory response