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Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee

We report the updated classification of Inborn Errors of Immunity/Primary Immunodeficiencies, compiled by the International Union of Immunological Societies Expert Committee. This report documents the key clinical and laboratory features of 430 inborn errors of immunity, including 64 gene defects th...

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Autores principales: Tangye, Stuart G., Al-Herz, Waleed, Bousfiha, Aziz, Chatila, Talal, Cunningham-Rundles, Charlotte, Etzioni, Amos, Franco, Jose Luis, Holland, Steven M., Klein, Christoph, Morio, Tomohiro, Ochs, Hans D., Oksenhendler, Eric, Picard, Capucine, Puck, Jennifer, Torgerson, Troy R., Casanova, Jean-Laurent, Sullivan, Kathleen E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082301/
https://www.ncbi.nlm.nih.gov/pubmed/31953710
http://dx.doi.org/10.1007/s10875-019-00737-x
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author Tangye, Stuart G.
Al-Herz, Waleed
Bousfiha, Aziz
Chatila, Talal
Cunningham-Rundles, Charlotte
Etzioni, Amos
Franco, Jose Luis
Holland, Steven M.
Klein, Christoph
Morio, Tomohiro
Ochs, Hans D.
Oksenhendler, Eric
Picard, Capucine
Puck, Jennifer
Torgerson, Troy R.
Casanova, Jean-Laurent
Sullivan, Kathleen E.
author_facet Tangye, Stuart G.
Al-Herz, Waleed
Bousfiha, Aziz
Chatila, Talal
Cunningham-Rundles, Charlotte
Etzioni, Amos
Franco, Jose Luis
Holland, Steven M.
Klein, Christoph
Morio, Tomohiro
Ochs, Hans D.
Oksenhendler, Eric
Picard, Capucine
Puck, Jennifer
Torgerson, Troy R.
Casanova, Jean-Laurent
Sullivan, Kathleen E.
author_sort Tangye, Stuart G.
collection PubMed
description We report the updated classification of Inborn Errors of Immunity/Primary Immunodeficiencies, compiled by the International Union of Immunological Societies Expert Committee. This report documents the key clinical and laboratory features of 430 inborn errors of immunity, including 64 gene defects that have either been discovered in the past 2 years since the previous update (published January 2018) or were characterized earlier but have since been confirmed or expanded upon in subsequent studies. The application of next-generation sequencing continues to expedite the rapid identification of novel gene defects, rare or common; broaden the immunological and clinical phenotypes of conditions arising from known gene defects and even known variants; and implement gene-specific therapies. These advances are contributing to greater understanding of the molecular, cellular, and immunological mechanisms of disease, thereby enhancing immunological knowledge while improving the management of patients and their families. This report serves as a valuable resource for the molecular diagnosis of individuals with heritable immunological disorders and also for the scientific dissection of cellular and molecular mechanisms underlying inborn errors of immunity and related human diseases.
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spelling pubmed-70823012020-03-23 Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee Tangye, Stuart G. Al-Herz, Waleed Bousfiha, Aziz Chatila, Talal Cunningham-Rundles, Charlotte Etzioni, Amos Franco, Jose Luis Holland, Steven M. Klein, Christoph Morio, Tomohiro Ochs, Hans D. Oksenhendler, Eric Picard, Capucine Puck, Jennifer Torgerson, Troy R. Casanova, Jean-Laurent Sullivan, Kathleen E. J Clin Immunol Original Article We report the updated classification of Inborn Errors of Immunity/Primary Immunodeficiencies, compiled by the International Union of Immunological Societies Expert Committee. This report documents the key clinical and laboratory features of 430 inborn errors of immunity, including 64 gene defects that have either been discovered in the past 2 years since the previous update (published January 2018) or were characterized earlier but have since been confirmed or expanded upon in subsequent studies. The application of next-generation sequencing continues to expedite the rapid identification of novel gene defects, rare or common; broaden the immunological and clinical phenotypes of conditions arising from known gene defects and even known variants; and implement gene-specific therapies. These advances are contributing to greater understanding of the molecular, cellular, and immunological mechanisms of disease, thereby enhancing immunological knowledge while improving the management of patients and their families. This report serves as a valuable resource for the molecular diagnosis of individuals with heritable immunological disorders and also for the scientific dissection of cellular and molecular mechanisms underlying inborn errors of immunity and related human diseases. Springer US 2020-01-17 2020 /pmc/articles/PMC7082301/ /pubmed/31953710 http://dx.doi.org/10.1007/s10875-019-00737-x Text en © The Author(s) 2020, corrected publication 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Tangye, Stuart G.
Al-Herz, Waleed
Bousfiha, Aziz
Chatila, Talal
Cunningham-Rundles, Charlotte
Etzioni, Amos
Franco, Jose Luis
Holland, Steven M.
Klein, Christoph
Morio, Tomohiro
Ochs, Hans D.
Oksenhendler, Eric
Picard, Capucine
Puck, Jennifer
Torgerson, Troy R.
Casanova, Jean-Laurent
Sullivan, Kathleen E.
Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
title Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
title_full Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
title_fullStr Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
title_full_unstemmed Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
title_short Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
title_sort human inborn errors of immunity: 2019 update on the classification from the international union of immunological societies expert committee
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082301/
https://www.ncbi.nlm.nih.gov/pubmed/31953710
http://dx.doi.org/10.1007/s10875-019-00737-x
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