Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators
Summary: The immune system is highly diverse, but characterization of its genetic architecture has lagged behind the vast progress made by genome-wide association studies (GWASs) of emergent diseases. Our GWAS for 54 functionally relevant phenotypes of the adaptive immune system in 489 healthy indiv...
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Elsevier
2018-10-01
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Series: | Cell Reports |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2211124718314931 |
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Article |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Vasiliki Lagou Josselyn E. Garcia-Perez Ide Smets Lies Van Horebeek Marijne Vandebergh Liye Chen Klara Mallants Teresa Prezzemolo Kelly Hilven Stephanie Humblet-Baron Matthieu Moisse Philip Van Damme Guy Boeckxstaens Paul Bowness Bénédicte Dubois James Dooley Adrian Liston An Goris |
spellingShingle |
Vasiliki Lagou Josselyn E. Garcia-Perez Ide Smets Lies Van Horebeek Marijne Vandebergh Liye Chen Klara Mallants Teresa Prezzemolo Kelly Hilven Stephanie Humblet-Baron Matthieu Moisse Philip Van Damme Guy Boeckxstaens Paul Bowness Bénédicte Dubois James Dooley Adrian Liston An Goris Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators Cell Reports |
author_facet |
Vasiliki Lagou Josselyn E. Garcia-Perez Ide Smets Lies Van Horebeek Marijne Vandebergh Liye Chen Klara Mallants Teresa Prezzemolo Kelly Hilven Stephanie Humblet-Baron Matthieu Moisse Philip Van Damme Guy Boeckxstaens Paul Bowness Bénédicte Dubois James Dooley Adrian Liston An Goris |
author_sort |
Vasiliki Lagou |
title |
Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators |
title_short |
Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators |
title_full |
Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators |
title_fullStr |
Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators |
title_full_unstemmed |
Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators |
title_sort |
genetic architecture of adaptive immune system identifies key immune regulators |
publisher |
Elsevier |
series |
Cell Reports |
issn |
2211-1247 |
publishDate |
2018-10-01 |
description |
Summary: The immune system is highly diverse, but characterization of its genetic architecture has lagged behind the vast progress made by genome-wide association studies (GWASs) of emergent diseases. Our GWAS for 54 functionally relevant phenotypes of the adaptive immune system in 489 healthy individuals identifies eight genome-wide significant associations explaining 6%–20% of variance. Coding and splicing variants in PTPRC and COMMD10 are involved in memory T cell differentiation. Genetic variation controlling disease-relevant T helper cell subsets includes RICTOR and STON2 associated with Th2 and Th17, respectively, and the interferon-lambda locus controlling regulatory T cell proliferation. Early and memory B cell differentiation stages are associated with variation in LARP1B and SP4. Finally, the latrophilin family member ADGRL2 correlates with baseline pro-inflammatory interleukin-6 levels. Suggestive associations reveal mechanisms of autoimmune disease associations, in particular related to pro-inflammatory cytokine production. Pinpointing these key human immune regulators offers attractive therapeutic perspectives. : Lagou et al. identify genetic factors explaining interindividual variation in composition of the adaptive immune system. Factors pinpoint key human immune regulators controlling B and T cell differentiation and levels of disease-relevant T helper and regulatory cells. These findings shed light on mechanisms of autoimmune disease and offer therapeutic perspectives. Keywords: adaptive immune system, immune phenotype, genetics, association, genome-wide association, autoimmunity, susceptibility |
url |
http://www.sciencedirect.com/science/article/pii/S2211124718314931 |
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doaj-35cdeeb0f9534e9380dd0c9868623eb42020-11-24T21:14:46ZengElsevierCell Reports2211-12472018-10-01253798810.e6Genetic Architecture of Adaptive Immune System Identifies Key Immune RegulatorsVasiliki Lagou0Josselyn E. Garcia-Perez1Ide Smets2Lies Van Horebeek3Marijne Vandebergh4Liye Chen5Klara Mallants6Teresa Prezzemolo7Kelly Hilven8Stephanie Humblet-Baron9Matthieu Moisse10Philip Van Damme11Guy Boeckxstaens12Paul Bowness13Bénédicte Dubois14James Dooley15Adrian Liston16An Goris17KU Leuven Department of Neurosciences, Laboratory for Neuroimmunology, 3000 Leuven, Belgium; VIB Center for Brain & Disease Research, Laboratory for Translational Immunology, 3000 Leuven, Belgium; KU Leuven Department of Immunology and Microbiology, Laboratory for Translational Immunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, BelgiumVIB Center for Brain & Disease Research, Laboratory for Translational Immunology, 3000 Leuven, Belgium; KU Leuven Department of Immunology and Microbiology, Laboratory for Translational Immunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, BelgiumKU Leuven Department of Neurosciences, Laboratory for Neuroimmunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, Belgium; Department of Neurology, University Hospitals Leuven, 3000 Leuven, BelgiumKU Leuven Department of Neurosciences, Laboratory for Neuroimmunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, BelgiumKU Leuven Department of Neurosciences, Laboratory for Neuroimmunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, BelgiumBotnar Research Centre, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford OX3 7LD, UKKU Leuven Department of Neurosciences, Laboratory for Neuroimmunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, BelgiumVIB Center for Brain & Disease Research, Laboratory for Translational Immunology, 3000 Leuven, Belgium; KU Leuven Department of Immunology and Microbiology, Laboratory for Translational Immunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, BelgiumKU Leuven Department of Neurosciences, Laboratory for Neuroimmunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, BelgiumVIB Center for Brain & Disease Research, Laboratory for Translational Immunology, 3000 Leuven, Belgium; KU Leuven Department of Immunology and Microbiology, Laboratory for Translational Immunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, BelgiumLeuven Brain Institute (LBI), Leuven, Belgium; VIB Center for Brain & Disease Research, Laboratory of Neurobiology, 3000 Leuven, Belgium; KU Leuven Department of Neurosciences, Experimental Neurology, 3000 Leuven, BelgiumLeuven Brain Institute (LBI), Leuven, Belgium; Department of Neurology, University Hospitals Leuven, 3000 Leuven, Belgium; VIB Center for Brain & Disease Research, Laboratory of Neurobiology, 3000 Leuven, Belgium; KU Leuven Department of Neurosciences, Experimental Neurology, 3000 Leuven, BelgiumKU Leuven Department of Chronic Diseases, Metabolism and Ageing, Translational Research Center for GI Disorders (TARGID), 3000 Leuven, Belgium; Department of Gastroenterology, University Hospitals Leuven, 3000 Leuven, BelgiumBotnar Research Centre, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford OX3 7LD, UKKU Leuven Department of Neurosciences, Laboratory for Neuroimmunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, Belgium; Department of Neurology, University Hospitals Leuven, 3000 Leuven, BelgiumVIB Center for Brain & Disease Research, Laboratory for Translational Immunology, 3000 Leuven, Belgium; KU Leuven Department of Immunology and Microbiology, Laboratory for Translational Immunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, BelgiumVIB Center for Brain & Disease Research, Laboratory for Translational Immunology, 3000 Leuven, Belgium; KU Leuven Department of Immunology and Microbiology, Laboratory for Translational Immunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, Belgium; Corresponding authorKU Leuven Department of Neurosciences, Laboratory for Neuroimmunology, 3000 Leuven, Belgium; Leuven Brain Institute (LBI), Leuven, Belgium; Corresponding authorSummary: The immune system is highly diverse, but characterization of its genetic architecture has lagged behind the vast progress made by genome-wide association studies (GWASs) of emergent diseases. Our GWAS for 54 functionally relevant phenotypes of the adaptive immune system in 489 healthy individuals identifies eight genome-wide significant associations explaining 6%–20% of variance. Coding and splicing variants in PTPRC and COMMD10 are involved in memory T cell differentiation. Genetic variation controlling disease-relevant T helper cell subsets includes RICTOR and STON2 associated with Th2 and Th17, respectively, and the interferon-lambda locus controlling regulatory T cell proliferation. Early and memory B cell differentiation stages are associated with variation in LARP1B and SP4. Finally, the latrophilin family member ADGRL2 correlates with baseline pro-inflammatory interleukin-6 levels. Suggestive associations reveal mechanisms of autoimmune disease associations, in particular related to pro-inflammatory cytokine production. Pinpointing these key human immune regulators offers attractive therapeutic perspectives. : Lagou et al. identify genetic factors explaining interindividual variation in composition of the adaptive immune system. Factors pinpoint key human immune regulators controlling B and T cell differentiation and levels of disease-relevant T helper and regulatory cells. These findings shed light on mechanisms of autoimmune disease and offer therapeutic perspectives. Keywords: adaptive immune system, immune phenotype, genetics, association, genome-wide association, autoimmunity, susceptibilityhttp://www.sciencedirect.com/science/article/pii/S2211124718314931 |