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Full-Length Plasmodium falciparum Circumsporozoite Protein Administered with Long-Chain Poly(I·C) or the Toll-Like Receptor 4 Agonist Glucopyranosyl Lipid Adjuvant-Stable Emulsion Elicits Potent Antibody and CD4 + T Cell Immunity and Protection in Mice
- Source :
- Infection and Immunity. 81:789-800
- Publication Year :
- 2013
- Publisher :
- American Society for Microbiology, 2013.
-
Abstract
- The Plasmodium falciparum circumsporozoite (CS) protein (CSP) is a major vaccine target for preventing malaria infection. Thus, developing strong and durable antibody and T cell responses against CSP with novel immunogens and potent adjuvants may improve upon the success of current approaches. Here, we compare four distinct full-length P. falciparum CS proteins expressed in Escherichia coli or Pichia pastoris for their ability to induce immunity and protection in mice when administered with long-chain poly(I·C) [poly(I·C)LC] as an adjuvant. CS proteins expressed in E. coli induced high-titer antibody responses against the NANP repeat region and potent CSP-specific CD4 + T cell responses. Moreover, E. coli -derived CS proteins in combination with poly(I·C)LC induced potent multifunctional (interleukin 2-positive [IL-2 + ], tumor necrosis factor alpha-positive [TNF-α + ], gamma interferon-positive [IFN-γ + ]) CD4 + effector T cell responses in blood, in spleen, and particularly in liver. Using transgenic Plasmodium berghei expressing the repeat region of P. falciparum CSP [ Pb -CS( Pf )], we showed that there was a 1- to 4-log decrease in malaria rRNA in the liver following a high-dose challenge and ∼50% sterilizing protection with a low-dose challenge compared to control levels. Protection was directly correlated with high-level antibody titers but not CD4 + T cell responses. Finally, protective immunity was also induced using the Toll-like receptor 4 agonist glucopyranosyl lipid adjuvant-stable emulsion (GLA-SE) as the adjuvant, which also correlated with high antibody titers yet CD4 + T cell immunity that was significantly less potent than that with poly(I·C)LC. Overall, these data suggest that full-length CS proteins and poly(I·C)LC or GLA-SE offer a simple vaccine formulation to be used alone or in combination with other vaccines for preventing malaria infection.
- Subjects :
- biology
T cell
medicine.medical_treatment
Immunology
Antibody titer
Plasmodium falciparum
biology.organism_classification
Microbiology
Molecular biology
Circumsporozoite protein
Infectious Diseases
medicine.anatomical_structure
Immunity
biology.protein
medicine
Parasitology
Plasmodium berghei
Antibody
Adjuvant
Subjects
Details
- ISSN :
- 10985522 and 00199567
- Volume :
- 81
- Database :
- OpenAIRE
- Journal :
- Infection and Immunity
- Accession number :
- edsair.doi...........cd115f5de7f8293d8b3f75baf008248e
- Full Text :
- https://doi.org/10.1128/iai.01108-12