Naturally Acquired Antibody Responses to a Synthetic Malaria Antigen AS202.11

Background. A major challenge to malaria vaccine development is identification of protective epitopes and respective protective immune responses. Objective. To characterize naturally acquired Immunoglobulin G (IgG) responses to the synthetic peptide AS202.11, a malaria vaccine candidate. Methodology...

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Main Authors: Rebeka Nazareth, Pius Horumpende, Tolbert Sonda, Arnold Ndaro, Edson Mollel, Eliakim Paul, Emmanuel Athanase, Jaffu Chilongola
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Journal of Tropical Medicine
Online Access:http://dx.doi.org/10.1155/2017/6843701
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author Rebeka Nazareth
Pius Horumpende
Tolbert Sonda
Arnold Ndaro
Edson Mollel
Eliakim Paul
Emmanuel Athanase
Jaffu Chilongola
author_facet Rebeka Nazareth
Pius Horumpende
Tolbert Sonda
Arnold Ndaro
Edson Mollel
Eliakim Paul
Emmanuel Athanase
Jaffu Chilongola
author_sort Rebeka Nazareth
collection DOAJ
description Background. A major challenge to malaria vaccine development is identification of protective epitopes and respective protective immune responses. Objective. To characterize naturally acquired Immunoglobulin G (IgG) responses to the synthetic peptide AS202.11, a malaria vaccine candidate. Methodology. This community based cross-sectional study enrolled 320 participants aged 1 year and above. Demographic information was recorded through interviews. Detection of P. falciparum infection was done by microscopy, malaria rapid diagnostic test, and polymerase chain reaction. ELISA was used to detect IgG antibody. Data was analyzed using STATA. Results. The overall AS202.11 IgG seropositivity was 78.8% (73.9–82.9). Seropositivity by age categories was ≤12 years [74.3% (67.4–80.2)], 13–40 years [85.3% (76.5–91.1)], and >40 years [82.6% (68.7–91.1)]. Compared to the ≤ 12-year-old group, aORs for the other groups were 2.22 (1.14–4.32), p=0.019, and 1.87 (0.81–4.35), p=0.143, for the 13–40-year-old and >40-year-old groups, respectively. The 13–40-year-old group had more seropositive individuals compared to the ≤ 12-year-old group. Conclusion. We report a high degree of recognition of AS202.11 by IgG elicited by field P. falciparum strains, suggesting its close similarity to native P. falciparum antigens and possible suitability of the peptide as a future malaria vaccine candidate.
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spelling doaj-art-548e54dfd38b470a8e112c9da3e878a62025-02-03T00:59:51ZengWileyJournal of Tropical Medicine1687-96861687-96942017-01-01201710.1155/2017/68437016843701Naturally Acquired Antibody Responses to a Synthetic Malaria Antigen AS202.11Rebeka Nazareth0Pius Horumpende1Tolbert Sonda2Arnold Ndaro3Edson Mollel4Eliakim Paul5Emmanuel Athanase6Jaffu Chilongola7Kilimanjaro Christian Medical University College, P.O. Box 2240, Moshi, TanzaniaKilimanjaro Christian Medical University College, P.O. Box 2240, Moshi, TanzaniaKilimanjaro Christian Medical University College, P.O. Box 2240, Moshi, TanzaniaKilimanjaro Clinical Research Institute, P.O. Box 2236, Moshi, TanzaniaKibong’oto Infectious Diseases Hospital, P.O. Box 12, Sanya Juu, Siha, TanzaniaKilimanjaro Christian Medical University College, P.O. Box 2240, Moshi, TanzaniaNewala Town Council Hospital, P.O. Box 39, Newala, TanzaniaKilimanjaro Christian Medical University College, P.O. Box 2240, Moshi, TanzaniaBackground. A major challenge to malaria vaccine development is identification of protective epitopes and respective protective immune responses. Objective. To characterize naturally acquired Immunoglobulin G (IgG) responses to the synthetic peptide AS202.11, a malaria vaccine candidate. Methodology. This community based cross-sectional study enrolled 320 participants aged 1 year and above. Demographic information was recorded through interviews. Detection of P. falciparum infection was done by microscopy, malaria rapid diagnostic test, and polymerase chain reaction. ELISA was used to detect IgG antibody. Data was analyzed using STATA. Results. The overall AS202.11 IgG seropositivity was 78.8% (73.9–82.9). Seropositivity by age categories was ≤12 years [74.3% (67.4–80.2)], 13–40 years [85.3% (76.5–91.1)], and >40 years [82.6% (68.7–91.1)]. Compared to the ≤ 12-year-old group, aORs for the other groups were 2.22 (1.14–4.32), p=0.019, and 1.87 (0.81–4.35), p=0.143, for the 13–40-year-old and >40-year-old groups, respectively. The 13–40-year-old group had more seropositive individuals compared to the ≤ 12-year-old group. Conclusion. We report a high degree of recognition of AS202.11 by IgG elicited by field P. falciparum strains, suggesting its close similarity to native P. falciparum antigens and possible suitability of the peptide as a future malaria vaccine candidate.http://dx.doi.org/10.1155/2017/6843701
spellingShingle Rebeka Nazareth
Pius Horumpende
Tolbert Sonda
Arnold Ndaro
Edson Mollel
Eliakim Paul
Emmanuel Athanase
Jaffu Chilongola
Naturally Acquired Antibody Responses to a Synthetic Malaria Antigen AS202.11
Journal of Tropical Medicine
title Naturally Acquired Antibody Responses to a Synthetic Malaria Antigen AS202.11
title_full Naturally Acquired Antibody Responses to a Synthetic Malaria Antigen AS202.11
title_fullStr Naturally Acquired Antibody Responses to a Synthetic Malaria Antigen AS202.11
title_full_unstemmed Naturally Acquired Antibody Responses to a Synthetic Malaria Antigen AS202.11
title_short Naturally Acquired Antibody Responses to a Synthetic Malaria Antigen AS202.11
title_sort naturally acquired antibody responses to a synthetic malaria antigen as202 11
url http://dx.doi.org/10.1155/2017/6843701
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