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Functional Comparison of Blood-Stage Plasmodium falciparum Malaria Vaccine Candidate Antigens.
Illingworth, Joseph J; Alanine, Daniel G; Brown, Rebecca; Marshall, Jennifer M; Bartlett, Helen E; Silk, Sarah E; Labbé, Geneviève M; Quinkert, Doris; Cho, Jee Sun; Wendler, Jason P; Pattinson, David J; Barfod, Lea; Douglas, Alexander D; Shea, Michael W; Wright, Katherine E; de Cassan, Simone C; Higgins, Matthew K; Draper, Simon J.
Afiliação
  • Illingworth JJ; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Alanine DG; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Brown R; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Marshall JM; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Bartlett HE; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Silk SE; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Labbé GM; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Quinkert D; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Cho JS; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Wendler JP; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Pattinson DJ; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Barfod L; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Douglas AD; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Shea MW; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Wright KE; Department of Biochemistry, University of Oxford, Oxford, United Kingdom.
  • de Cassan SC; Jenner Institute, University of Oxford, Oxford, United Kingdom.
  • Higgins MK; Department of Biochemistry, University of Oxford, Oxford, United Kingdom.
  • Draper SJ; Jenner Institute, University of Oxford, Oxford, United Kingdom.
Front Immunol ; 10: 1254, 2019.
Article em En | MEDLINE | ID: mdl-31214195
ABSTRACT
The malaria genome encodes over 5,000 proteins and many of these have also been proposed to be potential vaccine candidates, although few of these have been tested clinically. RH5 is one of the leading blood-stage Plasmodium falciparum malaria vaccine antigens and Phase I/II clinical trials of vaccines containing this antigen are currently underway. Its likely mechanism of action is to elicit antibodies that can neutralize merozoites by blocking their invasion of red blood cells (RBC). However, many other antigens could also elicit neutralizing antibodies against the merozoite, and most of these have never been compared directly to RH5. The objective of this study was to compare a range of blood-stage antigens to RH5, to identify any antigens that outperform or synergize with anti-RH5 antibodies. We selected 55 gene products, covering 15 candidate antigens that have been described in the literature and 40 genes selected on the basis of bioinformatics functional prediction. We were able to make 20 protein-in-adjuvant vaccines from the original selection. Of these, S-antigen and CyRPA robustly elicited antibodies with neutralizing properties. Anti-CyRPA IgG generally showed additive GIA with anti-RH5 IgG, although high levels of anti-CyRPA-specific rabbit polyclonal IgG were required to achieve 50% GIA. Our data suggest that further vaccine antigen screening efforts are required to identify a second merozoite target with similar antibody-susceptibility to RH5.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasmodium falciparum / Malária Falciparum / Vacinas Antimaláricas / Eritrócitos / Merozoítos Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasmodium falciparum / Malária Falciparum / Vacinas Antimaláricas / Eritrócitos / Merozoítos Idioma: En Ano de publicação: 2019 Tipo de documento: Article