Naturally occurring mutation affecting the MyD88-binding site ofTNFRSF13Bimpairs triggering of class switch recombination

Viral Double-Stranded RNA Triggers Ig Class Switching by Activating Upper Respiratory Mucosa B Cells through an Innate TLR3 Pathway Involving BAFF

(2014) W. Xu et al.   JOURNAL OF IMMUNOLOGY

Toll-like receptor 9, transmembrane activator and calcium-modulating cyclophilin ligand interactor, and CD40 synergize in causing B-cell activation

(2011) Esra Ozcan et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Functional analysis of transmembrane activator and calcium-modulating cyclophilin ligand interactor (TACI) mutations associated with common variable immunodeficiency

(2011) Ari J. Fried et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Immunological Characteristics and Two Novel Mutations in TACI in a Cohort of 28 Pediatric Patients with Common Variable Immunodeficiency

(2011) María B. Almejún et al.   JOURNAL OF CLINICAL IMMUNOLOGY

T cells and follicular dendritic cells in germinal center B-cell formation and selection

(2010) Carola G. Vinuesa et al.   IMMUNOLOGICAL REVIEWS

Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation

(2010) Aude Magerus-Chatinet et al.   JOURNAL OF CLINICAL INVESTIGATION

The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88

(2010) Bing He et al.   NATURE IMMUNOLOGY

The murine equivalent of the A181E TACI mutation associated with common variable immunodeficiency severely impairs B-cell function

(2009) J. J. Lee et al.   BLOOD

Toll-like receptor 7 and 9 defects in common variable immunodeficiency

(2009) Joyce E. Yu et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Novel Mutations in TACI (TNFRSF13B) Causing Common Variable Immunodeficiency

(2009) Javad Mohammadi et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Mechanism and Regulation of Class Switch Recombination

(2008) Janet Stavnezer et al.   Annual Review of Immunology

Response: Improving classification in CVID

(2008) C. Wehr et al.   BLOOD

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

(2008) U. Salzer et al.   BLOOD