An Expression Quantitative Trait Locus of Fc Gamma Receptor Genes is Associated with Anti-Malarial IgG Responses and Infection Levels in Burkinabe Families.

Plasmodium falciparum immunization FCGR Expression Quantitative Trait Locus FCGR gene polymorphism Fc Gamma Receptors Malaria- blood infectious levels

Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
25 Oct 2024
Historique:
received: 21 08 2024
revised: 01 10 2024
accepted: 22 10 2024
medline: 25 10 2024
pubmed: 25 10 2024
entrez: 25 10 2024
Statut: aheadofprint

Résumé

The interaction between antibodies and Fc gamma receptors (FcγRs) plays a critical role in regulating immune responses to Plasmodium falciparum. Polymorphisms in genes encoding FcγRs influence the host's capacity to control parasite infection. This study investigates whether non-coding variants influencing FcγR expression are associated with anti-malarial immunization and infection traits. We utilized eQTL databases and functional annotations to identify non-coding variants, specifically rs1771575, rs2099684, and rs6700241, within the FCGR gene cluster. In addition, we examined the coding variants rs1801274 (p.His167Arg) and rs1050501 (p.Ile231Thr), which affect the affinity of FcγRIIa and FcγRIIb for IgG. These variants were genotyped in 163 individuals from Burkinabe families. Family-based linear mixed regression and Quantitative Transmission Disequilibrium Tests (QTDT) analyses were performed to assess associations with IgG levels and malaria infection, accounting for relevant covariates. Linear mixed models identified rs1771575 as associated with total IgG levels, while both rs1771575 and rs1801274 were linked to IgG2, and rs1050501 to IgG1 levels. A haplotype combining rs2099684 and rs6700241 was positively associated with IgG1. The rs1771575-CC and rs1050501-TT genotypes correlated with higher infection levels in children. QTDT models confirmed the association of rs1771575 with IgG2 and infection in children. Our findings suggest that the intergenic variant rs1771575 serves as an independent marker for IgG levels and blood infection in children. This highlights the interplay between regulatory variants and coding mutations in FCGR, which may influence immune function and antibody production. These results underscore the potential for personalized strategies to monitor humoral responses in malaria-endemic regions.

Sections du résumé

BACKGROUND BACKGROUND
The interaction between antibodies and Fc gamma receptors (FcγRs) plays a critical role in regulating immune responses to Plasmodium falciparum. Polymorphisms in genes encoding FcγRs influence the host's capacity to control parasite infection. This study investigates whether non-coding variants influencing FcγR expression are associated with anti-malarial immunization and infection traits.
METHODS METHODS
We utilized eQTL databases and functional annotations to identify non-coding variants, specifically rs1771575, rs2099684, and rs6700241, within the FCGR gene cluster. In addition, we examined the coding variants rs1801274 (p.His167Arg) and rs1050501 (p.Ile231Thr), which affect the affinity of FcγRIIa and FcγRIIb for IgG. These variants were genotyped in 163 individuals from Burkinabe families. Family-based linear mixed regression and Quantitative Transmission Disequilibrium Tests (QTDT) analyses were performed to assess associations with IgG levels and malaria infection, accounting for relevant covariates.
RESULTS RESULTS
Linear mixed models identified rs1771575 as associated with total IgG levels, while both rs1771575 and rs1801274 were linked to IgG2, and rs1050501 to IgG1 levels. A haplotype combining rs2099684 and rs6700241 was positively associated with IgG1. The rs1771575-CC and rs1050501-TT genotypes correlated with higher infection levels in children. QTDT models confirmed the association of rs1771575 with IgG2 and infection in children.
CONCLUSIONS CONCLUSIONS
Our findings suggest that the intergenic variant rs1771575 serves as an independent marker for IgG levels and blood infection in children. This highlights the interplay between regulatory variants and coding mutations in FCGR, which may influence immune function and antibody production. These results underscore the potential for personalized strategies to monitor humoral responses in malaria-endemic regions.

Identifiants

pubmed: 39450553
pii: 7840803
doi: 10.1093/infdis/jiae528
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Christelle Dieppois (C)

Aix Marseille Univ, INSERM U1090, TAGC, Marseille 13009, France.

Mathieu Adjemout (M)

Aix Marseille Univ, INSERM U1090, TAGC, Marseille 13009, France.

Jules Cretin (J)

Aix Marseille Univ, INSERM U1090, TAGC, Marseille 13009, France.

Frederic Gallardo (F)

Aix Marseille Univ, INSERM U1090, TAGC, Marseille 13009, France.

Magali Torres (M)

Aix Marseille Univ, INSERM U1090, TAGC, Marseille 13009, France.

Christophe Picard (C)

Aix Marseille Univ, CNRS, EFS, ADES, Marseille 13005, France.
Immunogenetics Laboratory, Etablissement Français du Sang PACA-Corse, Marseille 13005, France.

Serge Aimé Sawadogo (SA)

Université Joseph KI-ZERBO, Unité de Formation en Sciences de la Santé (UFR/SDS), 03 BP 7021 Ouagadougou 03.
Centre PrïmO-Nelson Mandela, 84 rue Sao Tomé et Principe, 09 BP 706 Ouagadougou 09.

Pascal Rihet (P)

Aix Marseille Univ, INSERM U1090, TAGC, Marseille 13009, France.

Pascale Paul (P)

Aix Marseille Univ, INSERM U1090, TAGC, Marseille 13009, France.

Classifications MeSH