Analysis of antibody responses to selected Plasmodium falciparum merozoite surface antigens in mild and cerebral malaria and associations with clinical outcomes.


Journal

Clinical and experimental immunology
ISSN: 1365-2249
Titre abrégé: Clin Exp Immunol
Pays: England
ID NLM: 0057202

Informations de publication

Date de publication:
04 2019
Historique:
accepted: 13 12 2018
pubmed: 24 12 2018
medline: 18 2 2020
entrez: 24 12 2018
Statut: ppublish

Résumé

Merozoite surface proteins (MSPs) are critical for parasite invasion; they represent attractive targets for antibody-based protection against clinical malaria. To identify protection-associated target MSPs, the present study analysed antibody responses to whole merozoite extract (ME) and to defined MSP recombinant antigens in hospitalized patients from a low endemic urban area as a function of disease severity (mild versus cerebral malaria). Sera from 110 patients with confirmed severe cerebral malaria (CM) and 91 patients with mild malaria (MM) were analysed (mean age = 29 years) for total and subclass immunoglobulin (Ig)G to ME and total IgG to MSP1p19, MSP2, MSP3, MSP4 and MSP5 by enzyme-linked immunosorbent assay (ELISA). Functional antibody responses were evaluated using the antibody-dependent respiratory burst (ADRB) assay in a subset of sera. There was a trend towards higher IgG1 and IgG4 levels to ME in CM compared to MM; only ME IgM responses differed significantly between fatal and surviving CM patients. Increased prevalence of IgG to individual MSPs was found in the CM compared to the MM group, including significantly higher levels of IgG to MSP4 and MSP5 in the former. Sera from fatal (24·5%) versus surviving cases showed significantly lower IgG to MSP1p19 and MSP3 (P < 0·05). ADRB assay readouts correlated with high levels of anti-MSP IgG, and trended higher in sera from patients with surviving compared to fatal CM outcome (P = 0·07). These results document strong differential antibody responses to MSP antigens as targets of protective immunity against CM and in particular MSP1p19 and MSP3 as prognostic indicators.

Identifiants

pubmed: 30580455
doi: 10.1111/cei.13254
pmc: PMC6422657
doi:

Substances chimiques

Antibodies, Protozoan 0
Antigens, Protozoan 0
Cell Extracts 0
Immunoglobulin M 0
Merozoite Surface Protein 1 0
Recombinant Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

86-96

Informations de copyright

© 2018 British Society for Immunology.

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Auteurs

B Mbengue (B)

Service d'Immunologie FMPO, Université Cheikh Anta Diop de Dakar, Senegal.
Unité d'Immunogénétique, Institut Pasteur de Dakar, IPD, Senegal.

M M Fall (MM)

Service de Réanimation, Hôpital Principal de Dakar, HPD, Senegal.

M-L Varela (ML)

Unité d'Immunologie, Institut Pasteur de Dakar, IPD, Senegal.

C Loucoubar (C)

Groupe de Biostatistique et Bioinformatique, IPD, Senegal.

C Joos (C)

Unité d'Immunologie, Institut Pasteur de Dakar, IPD, Senegal.

B Fall (B)

Fédération des Laboratoires, Hôpital Principal de Dakar, HPD, Senegal.

M S Niang (MS)

Service d'Immunologie FMPO, Université Cheikh Anta Diop de Dakar, Senegal.

B Niang (B)

Service de Réanimation, Hôpital Principal de Dakar, HPD, Senegal.

M Mbow (M)

Service d'Immunologie FMPO, Université Cheikh Anta Diop de Dakar, Senegal.

A Dieye (A)

Service d'Immunologie FMPO, Université Cheikh Anta Diop de Dakar, Senegal.
Unité d'Immunogénétique, Institut Pasteur de Dakar, IPD, Senegal.

R Perraut (R)

Unité d'Immunogénétique, Institut Pasteur de Dakar, IPD, Senegal.
Unité d'Immunologie, Institut Pasteur de Dakar, IPD, Senegal.

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