Correction: an immunogenomic exome landscape of triple positive primary antiphospholipid patients

Correction: an immunogenomic exome landscape of triple positive primary antiphospholipid patients

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Correction to: _Genes & Immunity_ https://doi.org/10.1038/s41435-024-00255-w, published online 24 January 2024 In this article the affiliation details for A. Cobat and B. Boisson were incorrectly given as: A. Cobat4, B. Boisson4,5, but should have been: A. Cobat4,5,13, B. Boisson4,5,8,13, Two duplicate sentences have been deleted from the original abstract, which now reads as follows: Primary antiphospholipid syndrome is characterized by thrombosis and autoantibodies directed against phospholipids or associated proteins. The genetic etiology of PAPS remains unknown. We enrolled 21 patients with thromboembolic events associated to lupus anticoagulant, anticardiolipin and anti β2 glycoprotein1 autoantibodies. We performed whole exome sequencing and a systematic variant-based analysis in genes associated with thrombosis, in candidate genes previously associated with APS or inborn errors of immunity. Data were compared to public databases and to a control cohort of 873 non-autoimmune patients. Variants were identified following a state-of-the-art pipeline. Enrichment analysis was performed by comparing with the control cohort. We found an absence of significant HLA bias and genetic heterogeneity in these patients, including when testing combinations of rare variants in genes encoding for proteins involved in thrombosis and of variants in genes linked with inborn errors of immunity. These results provide evidence of genetic heterogeneity in PAPS, even in a homogenous series of triple-positive patients. At the individual scale, a combination of variants may participate to the breakdown of B cell tolerance and to the vessel damage. The original article has been corrected. AUTHOR INFORMATION Author notes * These authors contributed equally: A. Cobat, B. Boisson, R. Carapito, A. S. Korganow AUTHORS AND AFFILIATIONS * Department of Clinical Immunology and Internal Medicine, National Reference Center for Systemic Autoimmune Diseases (CNR RESO), Tertiary Center for Primary Immunodeficiency, Strasbourg University Hospital, F-67000, Strasbourg, France A. Guffroy, L. Jacquel, V. Poindron, V. Delannoy, P. Soulas-Sprauel, T. Martin, V. Gies & A. S. Korganow * University Strasbourg, INSERM UMR - S1109, Institut Thématique Interdisciplinaire (ITI) de Médecine de Précision de Strasbourg, Transplantex NG, Fédération Hospitalo-Universitaire OMICARE, Fédération de Médecine Translationnelle de Strasbourg (FMTS), F-67000, Strasbourg, France A. Guffroy, N. Paul, A. Molitor, P. Soulas-Sprauel, T. Martin, S. Bahram, V. Gies, R. Carapito & A. S. Korganow * University de Strasbourg, Faculty of Medicine, F-67000, Strasbourg, France A. Guffroy, L. Jacquel, T. Martin, R. Carapito & A. S. Korganow * University Paris-Cité, Imagine Institute, F-75015, Paris, France Y. Seeleuthner, J. L. Casanova, A. Cobat & B. Boisson * Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France Y. Seeleuthner, J. L. Casanova, A. Cobat & B. Boisson * Department of Internal Medicine, Belle-Isle Hospital, Metz, France F. Maurier * Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital Universitaire, Strasbourg, France A. C. Voegeli * St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA P. Zhang, J. L. Casanova & B. Boisson * Laboratoire d’Immunologie, Plateau Technique de Biologie, Hôpital Universitaire, Strasbourg, France B. Nespola * Laboratoire d’exploration du HLA, Centre de Transfusion Sanguine, Strasbourg, France M. J. Apithy * University Strasbourg, Faculty of Pharmacy, F-67400, Illkirch, France P. Soulas-Sprauel * Department of Rheumatology and Clinical Immunology, Medical Center—University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany R. E. Voll Authors * A. Guffroy View author publications You can also search for this author inPubMed Google Scholar * L. Jacquel View author publications You can also search for this author inPubMed Google Scholar * Y. Seeleuthner View author publications You can also search for this author inPubMed Google Scholar * N. Paul View author publications You can also search for this author inPubMed Google Scholar * V. Poindron View author publications You can also search for this author inPubMed Google Scholar * F. Maurier View author publications You can also search for this author inPubMed Google Scholar * V. Delannoy View author publications You can also search for this author inPubMed Google Scholar * A. C. Voegeli View author publications You can also search for this author inPubMed Google Scholar * P. Zhang View author publications You can also search for this author inPubMed Google Scholar * B. Nespola View author publications You can also search for this author inPubMed Google Scholar * A. Molitor View author publications You can also search for this author inPubMed Google Scholar * M. J. Apithy View author publications You can also search for this author inPubMed Google Scholar * P. Soulas-Sprauel View author publications You can also search for this author inPubMed Google Scholar * T. Martin View author publications You can also search for this author inPubMed Google Scholar * R. E. Voll View author publications You can also search for this author inPubMed Google Scholar * S. Bahram View author publications You can also search for this author inPubMed Google Scholar * V. Gies View author publications You can also search for this author inPubMed Google Scholar * J. L. Casanova View author publications You can also search for this author inPubMed Google Scholar * A. Cobat View author publications You can also search for this author inPubMed Google Scholar * B. Boisson View author publications You can also search for this author inPubMed Google Scholar * R. Carapito View author publications You can also search for this author inPubMed Google Scholar * A. S. Korganow View author publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHORS Correspondence to A. Guffroy or A. S. Korganow. ADDITIONAL INFORMATION The original article can be found online at https://doi.org/10.1038/s41435-024-00255-w. RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Guffroy, A., Jacquel, L., Seeleuthner, Y. _et al._ Correction: An immunogenomic exome landscape of triple positive primary antiphospholipid patients. _Genes Immun_ 25, 176 (2024). https://doi.org/10.1038/s41435-024-00261-y Download citation * Published: 19 March 2024 * Issue Date: April 2024 * DOI: https://doi.org/10.1038/s41435-024-00261-y SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative

Correction to: _Genes & Immunity_ https://doi.org/10.1038/s41435-024-00255-w, published online 24 January 2024 In this article the affiliation details for A. Cobat and B. Boisson were


incorrectly given as: A. Cobat4, B. Boisson4,5, but should have been: A. Cobat4,5,13, B. Boisson4,5,8,13, Two duplicate sentences have been deleted from the original abstract, which now


reads as follows: Primary antiphospholipid syndrome is characterized by thrombosis and autoantibodies directed against phospholipids or associated proteins. The genetic etiology of PAPS


remains unknown. We enrolled 21 patients with thromboembolic events associated to lupus anticoagulant, anticardiolipin and anti β2 glycoprotein1 autoantibodies. We performed whole exome


sequencing and a systematic variant-based analysis in genes associated with thrombosis, in candidate genes previously associated with APS or inborn errors of immunity. Data were compared to


public databases and to a control cohort of 873 non-autoimmune patients. Variants were identified following a state-of-the-art pipeline. Enrichment analysis was performed by comparing with


the control cohort. We found an absence of significant HLA bias and genetic heterogeneity in these patients, including when testing combinations of rare variants in genes encoding for


proteins involved in thrombosis and of variants in genes linked with inborn errors of immunity. These results provide evidence of genetic heterogeneity in PAPS, even in a homogenous series


of triple-positive patients. At the individual scale, a combination of variants may participate to the breakdown of B cell tolerance and to the vessel damage. The original article has been


corrected. AUTHOR INFORMATION Author notes * These authors contributed equally: A. Cobat, B. Boisson, R. Carapito, A. S. Korganow AUTHORS AND AFFILIATIONS * Department of Clinical Immunology


and Internal Medicine, National Reference Center for Systemic Autoimmune Diseases (CNR RESO), Tertiary Center for Primary Immunodeficiency, Strasbourg University Hospital, F-67000,


Strasbourg, France A. Guffroy, L. Jacquel, V. Poindron, V. Delannoy, P. Soulas-Sprauel, T. Martin, V. Gies & A. S. Korganow * University Strasbourg, INSERM UMR - S1109, Institut


Thématique Interdisciplinaire (ITI) de Médecine de Précision de Strasbourg, Transplantex NG, Fédération Hospitalo-Universitaire OMICARE, Fédération de Médecine Translationnelle de Strasbourg


(FMTS), F-67000, Strasbourg, France A. Guffroy, N. Paul, A. Molitor, P. Soulas-Sprauel, T. Martin, S. Bahram, V. Gies, R. Carapito & A. S. Korganow * University de Strasbourg, Faculty


of Medicine, F-67000, Strasbourg, France A. Guffroy, L. Jacquel, T. Martin, R. Carapito & A. S. Korganow * University Paris-Cité, Imagine Institute, F-75015, Paris, France Y.


Seeleuthner, J. L. Casanova, A. Cobat & B. Boisson * Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France Y. Seeleuthner, J. L. Casanova, A.


Cobat & B. Boisson * Department of Internal Medicine, Belle-Isle Hospital, Metz, France F. Maurier * Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital Universitaire,


Strasbourg, France A. C. Voegeli * St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA P. Zhang, J. L. Casanova 


& B. Boisson * Laboratoire d’Immunologie, Plateau Technique de Biologie, Hôpital Universitaire, Strasbourg, France B. Nespola * Laboratoire d’exploration du HLA, Centre de Transfusion


Sanguine, Strasbourg, France M. J. Apithy * University Strasbourg, Faculty of Pharmacy, F-67400, Illkirch, France P. Soulas-Sprauel * Department of Rheumatology and Clinical Immunology,


Medical Center—University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany R. E. Voll Authors * A. Guffroy View author publications You can also search for this


author inPubMed Google Scholar * L. Jacquel View author publications You can also search for this author inPubMed Google Scholar * Y. Seeleuthner View author publications You can also search


for this author inPubMed Google Scholar * N. Paul View author publications You can also search for this author inPubMed Google Scholar * V. Poindron View author publications You can also


search for this author inPubMed Google Scholar * F. Maurier View author publications You can also search for this author inPubMed Google Scholar * V. Delannoy View author publications You


can also search for this author inPubMed Google Scholar * A. C. Voegeli View author publications You can also search for this author inPubMed Google Scholar * P. Zhang View author


publications You can also search for this author inPubMed Google Scholar * B. Nespola View author publications You can also search for this author inPubMed Google Scholar * A. Molitor View


author publications You can also search for this author inPubMed Google Scholar * M. J. Apithy View author publications You can also search for this author inPubMed Google Scholar * P.


Soulas-Sprauel View author publications You can also search for this author inPubMed Google Scholar * T. Martin View author publications You can also search for this author inPubMed Google


Scholar * R. E. Voll View author publications You can also search for this author inPubMed Google Scholar * S. Bahram View author publications You can also search for this author inPubMed 


Google Scholar * V. Gies View author publications You can also search for this author inPubMed Google Scholar * J. L. Casanova View author publications You can also search for this author


inPubMed Google Scholar * A. Cobat View author publications You can also search for this author inPubMed Google Scholar * B. Boisson View author publications You can also search for this


author inPubMed Google Scholar * R. Carapito View author publications You can also search for this author inPubMed Google Scholar * A. S. Korganow View author publications You can also


search for this author inPubMed Google Scholar CORRESPONDING AUTHORS Correspondence to A. Guffroy or A. S. Korganow. ADDITIONAL INFORMATION The original article can be found online at


https://doi.org/10.1038/s41435-024-00255-w. RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Guffroy, A., Jacquel, L., Seeleuthner, Y. _et al._


Correction: An immunogenomic exome landscape of triple positive primary antiphospholipid patients. _Genes Immun_ 25, 176 (2024). https://doi.org/10.1038/s41435-024-00261-y Download citation


* Published: 19 March 2024 * Issue Date: April 2024 * DOI: https://doi.org/10.1038/s41435-024-00261-y SHARE THIS ARTICLE Anyone you share the following link with will be able to read this


content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative