TY - JOUR
T1 - Primary Immunodeficiency Diseases
T2 - an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015
AU - Picard, Capucine
AU - Al-Herz, Waleed
AU - Bousfiha, Aziz
AU - Casanova, Jean Laurent
AU - Chatila, Talal
AU - Conley, Mary Ellen
AU - Cunningham-Rundles, Charlotte
AU - Etzioni, Amos
AU - Holland, Steven M.
AU - Klein, Christoph
AU - Nonoyama, Shigeaki
AU - Ochs, Hans D.
AU - Oksenhendler, Eric
AU - Puck, Jennifer M.
AU - Sullivan, Kathleen E.
AU - Tang, Mimi L.K.
AU - Franco, Jose Luis
AU - Gaspar, H. Bobby
N1 - Publisher Copyright:
© 2015, The Author(s).
PY - 2015/11/1
Y1 - 2015/11/1
N2 - We report the updated classification of primary immunodeficiencies compiled by the Primary Immunodeficiency Expert Committee (PID EC) of the International Union of Immunological Societies (IUIS). In the two years since the previous version, 34 new gene defects are reported in this updated version. For each disorder, the key clinical and laboratory features are provided. In this new version we continue to see the increasing overlap between immunodeficiency, as manifested by infection and/or malignancy, and immune dysregulation, as manifested by auto-inflammation, auto-immunity, and/or allergy. There is also an increased number of genetic defects that lead to susceptibility to specific organisms which reflects the finely tuned nature of immune defense systems. This classification is the most up to date catalogue of all known and published primary immunodeficiencies and acts as a current reference of the knowledge of these conditions and is an important aid for the genetic and molecular diagnosis of patients with these rare diseases.
AB - We report the updated classification of primary immunodeficiencies compiled by the Primary Immunodeficiency Expert Committee (PID EC) of the International Union of Immunological Societies (IUIS). In the two years since the previous version, 34 new gene defects are reported in this updated version. For each disorder, the key clinical and laboratory features are provided. In this new version we continue to see the increasing overlap between immunodeficiency, as manifested by infection and/or malignancy, and immune dysregulation, as manifested by auto-inflammation, auto-immunity, and/or allergy. There is also an increased number of genetic defects that lead to susceptibility to specific organisms which reflects the finely tuned nature of immune defense systems. This classification is the most up to date catalogue of all known and published primary immunodeficiencies and acts as a current reference of the knowledge of these conditions and is an important aid for the genetic and molecular diagnosis of patients with these rare diseases.
KW - Primary immunodeficiencies
KW - classification
KW - genetic defects
UR - http://www.scopus.com/inward/record.url?scp=84948581722&partnerID=8YFLogxK
U2 - 10.1007/s10875-015-0201-1
DO - 10.1007/s10875-015-0201-1
M3 - Article
C2 - 26482257
AN - SCOPUS:84948581722
SN - 0271-9142
VL - 35
SP - 696
EP - 726
JO - Journal of Clinical Immunology
JF - Journal of Clinical Immunology
IS - 8
ER -