TY - JOUR
T1 - Human Inborn Errors of Immunity
T2 - 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee
AU - Tangye, Stuart G.
AU - Al-Herz, Waleed
AU - Bousfiha, Aziz
AU - Cunningham-Rundles, Charlotte
AU - Franco, Jose Luis
AU - Holland, Steven M.
AU - Klein, Christoph
AU - Morio, Tomohiro
AU - Oksenhendler, Eric
AU - Picard, Capucine
AU - Puel, Anne
AU - Puck, Jennifer
AU - Seppänen, Mikko R.J.
AU - Somech, Raz
AU - Su, Helen C.
AU - Sullivan, Kathleen E.
AU - Torgerson, Troy R.
AU - Meyts, Isabelle
N1 - Publisher Copyright:
© 2022, The Author(s).
PY - 2022/10
Y1 - 2022/10
N2 - We report the updated classification of inborn errors of immunity, compiled by the International Union of Immunological Societies Expert Committee. This report documents the key clinical and laboratory features of 55 novel monogenic gene defects, and 1 phenocopy due to autoantibodies, that have either been discovered since the previous update (published January 2020) or were characterized earlier but have since been confirmed or expanded in subsequent studies. While variants in additional genes associated with immune diseases have been reported in the literature, this update includes only those that the committee assessed that reached the necessary threshold to represent novel inborn errors of immunity. There are now a total of 485 inborn errors of immunity. These advances in discovering the genetic causes of human immune diseases continue to significantly further our understanding of molecular, cellular, and immunological mechanisms of disease pathogenesis, thereby simultaneously enhancing immunological knowledge and improving patient diagnosis and management. This report is designed to serve as a resource for immunologists and geneticists pursuing the molecular diagnosis of individuals with heritable immunological disorders and for the scientific dissection of cellular and molecular mechanisms underlying monogenic and related human immune diseases.
AB - We report the updated classification of inborn errors of immunity, compiled by the International Union of Immunological Societies Expert Committee. This report documents the key clinical and laboratory features of 55 novel monogenic gene defects, and 1 phenocopy due to autoantibodies, that have either been discovered since the previous update (published January 2020) or were characterized earlier but have since been confirmed or expanded in subsequent studies. While variants in additional genes associated with immune diseases have been reported in the literature, this update includes only those that the committee assessed that reached the necessary threshold to represent novel inborn errors of immunity. There are now a total of 485 inborn errors of immunity. These advances in discovering the genetic causes of human immune diseases continue to significantly further our understanding of molecular, cellular, and immunological mechanisms of disease pathogenesis, thereby simultaneously enhancing immunological knowledge and improving patient diagnosis and management. This report is designed to serve as a resource for immunologists and geneticists pursuing the molecular diagnosis of individuals with heritable immunological disorders and for the scientific dissection of cellular and molecular mechanisms underlying monogenic and related human immune diseases.
KW - IUIS Committee update
KW - Inborn errors of immunity
KW - autoinflammatory disorders
KW - immune dysregulation
KW - primary immunodeficiencies
UR - https://www.scopus.com/pages/publications/85132745587
U2 - 10.1007/s10875-022-01289-3
DO - 10.1007/s10875-022-01289-3
M3 - Article
AN - SCOPUS:85132745587
SN - 0271-9142
VL - 42
SP - 1473
EP - 1507
JO - Journal of Clinical Immunology
JF - Journal of Clinical Immunology
IS - 7
ER -