Differential Effects of Environmental and Genetic Factors on T and B Cell Immune Traits

Raúl Aguirre‐Gamboa(University Medical Center Groningen), Irma Joosten(University Medical Center), Paulo C. M. Urbano(University Medical Center), Renate G. van der Molen(Radboud University Medical Center), Esther van Rijssen(Radboud University Medical Center), Bram van Cranenbroek(University Medical Center), Marije Oosting(University Medical Center), Sanne P. Smeekens(Radboud University Medical Center), Martin Jaeger(Radboud University Medical Center), Maria M. Zorro(University Medical Center Groningen), Sebo Withoff(University Medical Center Groningen), Antonius E. van Herwaarden(Radboud University Nijmegen), Fred C.G.J. Sweep(Radboud University Nijmegen), Romana T. Netea(Radboud University Nijmegen), Morris A. Swertz(University Medical Center Groningen), Lude Franke(University of Groningen), Ramnik J. Xavier(Broad Institute), Leo A. B. Joosten(University Medical Center), Mihai G. Netea(University Medical Center), Cisca Wijmenga(Oslo University Hospital), Vinod Kumar(University Medical Center Groningen), Yang Li(University Medical Center Groningen), Hans J. P. M. Koenen(Radboud University Nijmegen)
Cell Reports
November 1, 2016
Cited by 215Open Access
Full Text

Abstract

Effective immunity requires a complex network of cellular and humoral components that interact with each other and are influenced by different environmental and host factors. We used a systems biology approach to comprehensively assess the impact of environmental and genetic factors on immune cell populations in peripheral blood, including associations with immunoglobulin concentrations, from ∼500 healthy volunteers from the Human Functional Genomics Project. Genetic heritability estimation showed that variations in T cell numbers are more strongly driven by genetic factors, while B cell counts are more environmentally influenced. Quantitative trait loci (QTL) mapping identified eight independent genomic loci associated with leukocyte count variation, including four associations with T and B cell subtypes. The QTLs identified were enriched among genome-wide association study (GWAS) SNPs reported to increase susceptibility to immune-mediated diseases. Our systems approach provides insights into cellular and humoral immune trait variability in humans.


Related Papers

No related papers found

Powered by citation graph analysis