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

被引:63
作者
Kastenmueller, Kathrin [1 ,2 ]
Espinosa, Diego A. [3 ]
Trager, Lauren [1 ,2 ,7 ]
Stoyanov, Cristina [1 ,2 ,3 ]
Salazar, Andres M. [4 ]
Pokalwar, Santosh [5 ]
Singh, Sanjay [5 ]
Dutta, Sheetij [6 ]
Ockenhouse, Christian F. [6 ]
Zavala, Fidel [3 ]
Seder, Robert A. [1 ,2 ]
机构
[1] NIAID, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
[2] NIAID, Cellular Immunol Sect, NIH, Bethesda, MD 20892 USA
[3] Johns Hopkins Univ, Dept Mol Microbiol & Immunol, Bloomberg Sch Publ Hlth, Baltimore, MD USA
[4] Oncovir, Washington, DC USA
[5] Gennova Biopharmaceut Ltd, Pune, Maharashtra, India
[6] Walter Reed Army Inst Res, Div Malaria Vaccine Dev, Silver Spring, MD USA
[7] Virginia Polytech Inst & State Univ, Virginia Maryland Reg Coll Vet Med, Blacksburg, VA 24061 USA
关键词
CANDIDATE MALARIA VACCINE; STRANDED-RNA POLY(I-C); SPOROZOITE VACCINE; CONFERS PROTECTION; CUTTING EDGE; IMMUNOGENICITY; SAFETY; EFFICACY; RESPONSES; RTS; S;
D O I
10.1128/IAI.01108-12
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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-alpha(+)], gamma interferon-positive [IFN-gamma(+)]) 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 similar to 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.
引用
收藏
页码:789 / 800
页数:12
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