Lost in Translation: Lack of CD4 Expression due to a Novel Genetic Defect
Author(s) -
Andrea Lisco,
Peiying Ye,
Chun-Shu Wong,
Luxin Pei,
Amy P. Hsu,
Emily M. Mace,
Jordan S. Orange,
Silvia Lucena Lage,
Addison J. Ward,
Stephen A. Migueles,
Mark Connors,
Megan Anderson,
Clarisa M. Buckner,
Susan Moir,
Adam Rupert,
Alina DulauFlorea,
Princess U. Ogbogu,
Dylan T. Timberlake,
Luigi D. Notarangelo,
Stefania Pittaluga,
Roshini S. Abraham,
Irini Sereti
Publication year - 2021
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1093/infdis/jiab025
Subject(s) - cd8 , biology , germinal center , immunology , t cell , bone marrow , proband , translation (biology) , mutation , microbiology and biotechnology , genetics , gene , b cell , immune system , messenger rna , antibody
CD4 expression identifies a subset of mature T cells primarily assisting the germinal center reaction and contributing to CD8+ T-cell and B-cell activation, functions, and longevity. Herein, we present a family in which a novel variant disrupting the translation-initiation codon of the CD4 gene resulted in complete loss of membrane and plasma soluble CD4 in peripheral blood, lymph node, bone marrow, skin, and ileum of a homozygous proband. This inherited CD4 knockout disease illustrates the clinical and immunological features of a complete deficiency of any functional component of CD4 and its similarities and differences with other clinical models of primary or acquired loss of CD4+ T cells.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom