1. Immunization strategies against visceral leishmaniosis with the nucleosomal histones of Leishmania infantum encoded in DNA vaccine or pulsed in dendritic cells
- Author
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Carlos Alonso, Javier Carrión, and Cristina Folgueira
- Subjects
Adoptive cell transfer ,Protozoan Proteins ,Antibodies, Protozoan ,Antigens, Protozoan ,T-Lymphocytes, Regulatory ,DNA vaccination ,Histones ,Mice ,parasitic diseases ,Vaccines, DNA ,medicine ,Animals ,Leishmania infantum ,Mice, Inbred BALB C ,General Veterinary ,General Immunology and Microbiology ,biology ,Public Health, Environmental and Occupational Health ,Kinetoplastida ,Leishmaniasis ,Dendritic Cells ,Dendritic cell ,medicine.disease ,Leishmania ,biology.organism_classification ,Adoptive Transfer ,Virology ,Infectious Diseases ,Liver ,Immunization ,Immunoglobulin G ,Immunology ,Leishmaniasis, Visceral ,Molecular Medicine ,Female ,Spleen - Abstract
Immunization of BALB/c mice with a DNA vaccine encoding the nucleosomal histones from Leishmania infantum resulted in a complete failure of protection against visceral leishmaniosis (VL), whereas the adoptive transfer of bone marrow-derived dendritic cells pulsed with the same pathoantigens plays an essential role in controlling parasite growth in half of the cases. Reduction of the visceral parasite burden seems to be related to low persistence of regulatory T-cells in the spleen from vaccinated mice. These results provide clues for the optimization of this vaccine strategy with the four Leishmania nucleosomal histones against L. infantum infection.
- Published
- 2008
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