Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/114195
Title: Natural immune response to Plasmodium vivax alpha-helical coiled coil protein motifs and its association with the risk of P. vivax malaria
Author: Cespedes, Nora
Li Wai Suen, ConnieS.N.
Koepfli, Cristian
Franca, Camila T.
Felger, Ingrid
Nebie, Issa
Arevalo-Herrera, Myriam
Mueller, Ivo
Corradin, Giampietro
Herrera, Sócrates
Keywords: Plasmodium vivax
Resposta immunitària
Malària
Plasmodium vivax
Immune response
Malaria
Issue Date: 2017
Publisher: Public Library of Science (PLoS)
Abstract: Protein alpha-helical coiled coil structures are known to induce antibodies able to block critical functions in different pathogens. In a previous study, a total of 50 proteins of Plasmodium vivax erythrocytic asexual stages containing alpha-helical coiled coil structural motifs were identified in silico, and the corresponding peptides were chemically synthesized. A total of 43 peptides were recognized by naturally acquired antibodies in plasma samples from both Papua New Guinea (PNG) and Colombian adult donors. In this study, the association between IgG antibodies to these peptides and clinical immunity was further explored by measuring total IgG antibody levels to 24 peptides in baseline samples from a longitudinal study of children aged 1-3 years (n = 164) followed for 16 months. Samples were reactive to all peptides tested. Eight peptides were recognized by >50% of individuals, whereas only one peptide had < 20% reactivity. Children infected at baseline were seropositive to 23/24 peptides. No significant association was observed between antibody titers and age or molecular force of infection, suggesting that antibody levels had already reached an equilibrium. There was a strong association between antibody levels to all peptides and protection against P. vivax clinical episodes during the 16 months follow-up. These results suggest that the selected coiled coil antigens might be good markers of both exposure and acquired immunity to P. vivax malaria, and further preclinical investigation should be performed to determine their potential as P. vivax vaccine antigens.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1371/journal.pone.0179863
It is part of: PloS one, 2017, vol. 12, num. 6, 14 p.
Related resource: http://dx.doi.org/10.1371/journal.pone.0179863
URI: http://hdl.handle.net/2445/114195
ISSN: 1932-6203
Appears in Collections:Articles publicats en revistes (ISGlobal)

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