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Longitudinal analysis of antibody responses to Plasmodium vivax sporozoite antigens following natural infection.

作者信息

Thawornpan Pongsakorn, Nicholas Justin, Malee Chayapat, Kochayoo Piyawan, Wangriatisak Kittikorn, Tianpothong Pachara, Ntumngia Francis Babila, J Barnes Samantha, H Adams John, Chootong Patchanee

机构信息

Department of Clinical Microbiology and Applied Technology, Faculty of Medical Technology, Mahidol University, Bangkok, Thailand.

Center for Global Health and Interdisciplinary Research, College of Public Health, University of South Florida, Tampa, Florida, United States of America.

出版信息

PLoS Negl Trop Dis. 2024 Jan 26;18(1):e0011907. doi: 10.1371/journal.pntd.0011907. eCollection 2024 Jan.


DOI:10.1371/journal.pntd.0011907
PMID:38277340
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10817200/
Abstract

BACKGROUND: P. vivax malaria is a major global health burden hindering social and economic development throughout many tropical and sub-tropical countries. Pre-erythrocytic (PE) vaccines emerge as an attractive approach for the control and elimination of malaria infection. Therefore, evaluating the magnitude, longevity and prevalence of naturally acquired IgG antibody responses against PE candidate antigens is useful for vaccine design. METHODOLOGY/PRINCIPAL FINDINGS: The antigenicity of five recombinant PE antigens (PvCSP-VK210, PvSSP3, PvM2-MAEBL, PvCelTOS and PvSPECT1) was evaluated in plasma samples from individuals residing in low transmission areas in Thailand (Ranong and Chumphon Provinces). The samples were collected at the time of acute vivax malaria and 90, 270 and 360 days later. The prevalence, magnitude and longevity of total IgG and IgG subclasses were determined for each antigen using the longitudinal data. Our results showed that seropositivity of all tested PE antigens was detected during infection in at least some subjects; anti-PvCSP-VK210 and anti-PvCelTOS antibodies were the most frequent. Titers of these antibodies declined during the year of follow up, but notably seropositivity persisted. Among seropositive subjects at post-infection, high number of subjects possessed antibodies against PvCSP-VK210. Anti-PvSSP3 antibody responses had the longest half-life. IgG subclass profiling showed that the predominant subclasses were IgG1 and IgG3 (cytophilic antibodies), tending to remain detectable for at least 360 days after infection. CONCLUSIONS/SIGNIFICANCE: The present study demonstrated the magnitude and longevity of serological responses to multiple PE antigens of P. vivax after natural infection. This knowledge could contribute to the design of an effective P. vivax vaccine.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/a858aa485c89/pntd.0011907.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/8af947a5beac/pntd.0011907.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/6c75c4a6f0e1/pntd.0011907.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/82a4de421c87/pntd.0011907.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/d18500eb4a7c/pntd.0011907.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/a858aa485c89/pntd.0011907.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/8af947a5beac/pntd.0011907.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/6c75c4a6f0e1/pntd.0011907.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/82a4de421c87/pntd.0011907.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/d18500eb4a7c/pntd.0011907.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7552/10817200/a858aa485c89/pntd.0011907.g005.jpg

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Longitudinal analysis of antibody responses to Plasmodium vivax sporozoite antigens following natural infection.

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引用本文的文献

[1]
Polarization toward Tfh2 cell involved in development of MBC and antibody responses against Plasmodium vivax infection.

PLoS Negl Trop Dis. 2024-10

[2]
Development and longevity of naturally acquired antibody and memory B cell responses against Plasmodium vivax infection.

PLoS Negl Trop Dis. 2024-10

本文引用的文献

[1]
Identification of novel proteins associated with protection against clinical malaria.

Front Cell Infect Microbiol. 2023

[2]
Drug resistance of Plasmodium falciparum and Plasmodium vivax isolates in Indonesia.

Malar J. 2022-11-28

[3]
Longitudinal IgG antibody responses to Plasmodium vivax blood-stage antigens during and after acute vivax malaria in individuals living in the Brazilian Amazon.

PLoS Negl Trop Dis. 2022-11

[4]
Cross-reactive inhibitory antibody and memory B cell responses to variant strains of Duffy binding protein II at post-Plasmodium vivax infection.

PLoS One. 2022

[5]
Immunization with CSP and a RIG-I Agonist is Effective in Inducing a Functional and Protective Humoral Response Against .

Front Immunol. 2022

[6]
MAEBL Contributes to Sporozoite Adhesiveness.

Int J Mol Sci. 2022-5-20

[7]
Interferon-γ signal drives differentiation of T-bet atypical memory B cells into plasma cells following Plasmodium vivax infection.

Sci Rep. 2022-3-22

[8]
The presence of circulating antibody secreting cells and long-lived memory B cell responses to reticulocyte binding protein 1a in Plasmodium vivax patients.

Malar J. 2021-12-20

[9]
Protective effects of combining monoclonal antibodies and vaccines against the Plasmodium falciparum circumsporozoite protein.

PLoS Pathog. 2021-12

[10]
Seasonal Malaria Vaccination with or without Seasonal Malaria Chemoprevention.

N Engl J Med. 2021-9-9

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