Abstract
Plasmid DNA vaccines capable of preventing viral, bacterial, and parasitic infections are currently under development. Our labs have shown that a plasmid DNA vaccine encoding the circumsporozoite protein of the malaria parasite elicits protective immunity against live sporozoite challenge in adult BALB/c mice. We now find that the same DNA vaccine induces tolerance rather than immunity when administered to 2-5 d-old mice. Neonatally tolerized animals were unable to mount antibody, cytokine or cytotoxic responses when rechallenged with DNA vaccine in vitro or in vivo. Tolerance was specific for immunogenic epitopes expressed by the vaccine-encoded, endogenously produced antigen. Mice challenged with exogenous circumsporozoite protein produced antibodies against a different set of epitopes, and were not tolerized. These findings demonstrate important differences in the nature and specificity of the immune response elicited by DNA vaccines versus conventional protein immunogens.
MeSH Terms
Age Factors
Amino Acid Sequence
Animals
Cell Count
Cells, Cultured
Cloning, Molecular
DNA/immunology
Epitopes/chemistry,immunology
Female
Immune Tolerance/immunology
Immunization
Interferon-gamma/metabolism
Interleukin-4/metabolism
Malaria Vaccines/immunology
Mice
Mice, Inbred BALB C
Molecular Sequence Data
Peptide Fragments/chemistry,immunology
Plasmids/immunology
Plasmodium yoelii/immunology
Protozoan Proteins/chemistry,immunology
Spleen/metabolism
T-Lymphocytes, Cytotoxic/immunology,metabolism
Chemicals
Epitopes
Malaria Vaccines
Peptide Fragments
Protozoan Proteins
circumsporozoite protein, Protozoan
Interleukin-4
Interferon-gamma
DNA
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Mor G
Section of Retroviral Immunology, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland 20892, USA.
Yamshchikov G
Sedegah M
Takeno M
Wang R
Houghten R A
Hoffman S
Klinman D M
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