Immunodeficiency and bone marrow failure with mosaic and germline TLR8 gain of function

Inborn errors of immunity (IEI) are a genetically heterogeneous group of disorders with a broad clinical spectrum. Identification of molecular and functional bases of these disorders is important for diagnosis, treatment, and an understanding of the human immune response. We identified 6 unrelated m...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Blood 2021-05, Vol.137 (18), p.2450-2462
Hauptverfasser: Aluri, Jahnavi, Bach, Alicia, Kaviany, Saara, Chiquetto Paracatu, Luana, Kitcharoensakkul, Maleewan, Walkiewicz, Magdalena A., Putnam, Christopher D., Shinawi, Marwan, Saucier, Nermina, Rizzi, Elise M., Harmon, Michael T., Keppel, Molly P., Ritter, Michelle, Similuk, Morgan, Kulm, Elaine, Joyce, Michael, de Jesus, Adriana A., Goldbach-Mansky, Raphaela, Lee, Yi-Shan, Cella, Marina, Kendall, Peggy L., Dinauer, Mary C., Bednarski, Jeffrey J., Bemrich-Stolz, Christina, Canna, Scott W., Abraham, Shirley M., Demczko, Matthew M., Powell, Jonathan, Jones, Stacie M., Scurlock, Amy M., De Ravin, Suk See, Bleesing, Jack J., Connelly, James A., Rao, V. Koneti, Schuettpelz, Laura G., Cooper, Megan A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Inborn errors of immunity (IEI) are a genetically heterogeneous group of disorders with a broad clinical spectrum. Identification of molecular and functional bases of these disorders is important for diagnosis, treatment, and an understanding of the human immune response. We identified 6 unrelated males with neutropenia, infections, lymphoproliferation, humoral immune defects, and in some cases bone marrow failure associated with 3 different variants in the X-linked gene TLR8, encoding the endosomal Toll-like receptor 8 (TLR8). Interestingly, 5 patients had somatic variants in TLR8 with
ISSN:0006-4971
1528-0020
1528-0020
DOI:10.1182/blood.2020009620