Clarisa B. Sousa-De
Rio De Janeiro, RJ, Brazil
Last Updated: 09/26/2026
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Found 26 publications
The F1F3 recombinant chimera induced higher vaccine efficacy than its independent F1 and F3 components against Leishmania (L.) infantum chagasi mice infection.
Journal: Frontiers in immunology
Published: March 23, 2025
Design and development of highly conserved, HLA-promiscuous T cell multiepitope vaccines against human visceral leishmaniasis.
Journal: Frontiers in immunology
Published: December 06, 2024
CD4+ Th1 and Th17 responses and multifunctional CD8 T lymphocytes associated with cure or disease worsening in human visceral leishmaniasis.
Journal: Frontiers in immunology
Published: August 14, 2023
Multifunctional, TNF-α and IFN-γ-Secreting CD4 and CD8 T Cells and CD8High T Cells Are Associated With the Cure of Human Visceral Leishmaniasis.
Journal: Frontiers in immunology
Published: September 10, 2021
What Would Jenner and Pasteur Have Done About COVID-19 Coronavirus? The Urges of a Vaccinologist.
Journal: Frontiers in immunology
Published: May 20, 2020
The Delay in the Licensing of Protozoal Vaccines: A Comparative History.
Journal: Frontiers in immunology
Published: November 08, 2019
Nucleoside Hydrolase NH 36: A Vital Enzyme for the Leishmania Genus in the Development of T-Cell Epitope Cross-Protective Vaccines.
Journal: Frontiers in immunology
Published: December 11, 2018
The F1F3 Recombinant Chimera of Leishmania donovani-Nucleoside Hydrolase (NH36) and Its Epitopes Induce Cross-Protection Against Leishmania (V.) braziliensis Infection in Mice.
Journal: Frontiers in immunology
Published: October 27, 2018
Editorial: Epitope Discovery and Synthetic Vaccine Design.
Journal: Frontiers in immunology
Published: January 03, 2018
NH36 and F3 Antigen-Primed Dendritic Cells Show Preserved Migrating Capabilities and CCR7 Expression and F3 Is Effective in Immunotherapy of Visceral Leishmaniasis.
Journal: Frontiers in immunology
Published: August 03, 2017
Last Updated: 09/26/2026