Volume 120, Issue 5 , Pages 1178-1185, November 2007
Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: Clinical and immunologic outcomes in heterozygotes
Background
Mutations in the gene coding for transmembrane activator and calcium-modulating cyclophilin ligand interactor (TACI) have been identified in common variable immunodeficiency (CVID). Mutations coincided with immunodeficiency in families, suggesting dominant inheritance.
Objective
Because most subjects with CVID have no immunodeficient family members and heterozygous mutations predominate, the role of TACI mutations in sporadic CVID is unclear.
Methods
TACI was sequenced from the genomic DNA of 176 subjects with CVID and family members. B cells of subjects with or without mutations were examined for binding to the ligand, a proliferation inducing ligand (APRIL), and for proliferation and immunoglobulin production after ligand stimulation. Data analysis was performed to assess the clinical relevance of TACI mutations.
Results
Heterozygous TACI mutations were found in 13 subjects (7.3%). Six with mutations (46%) had episodes of autoimmune thrombocytopenia, in contrast with 12% of 163 subjects without mutations; splenomegaly and splenectomy were significantly increased (P = .012; P = .001.) B cells of some had impaired binding of APRIL and on culture with this ligand were defective in proliferation and immunoglobulin production; however, this was not different from B cells of subjects without mutations. Eight first-degree relatives from 5 families had the same mutations but were not immune-deficient, and their B cells produced normal amounts of IgG and IgA after APRIL stimulation.
Conclusion
Mutations in TACI significantly predispose to autoimmunity and lymphoid hyperplasia in CVID, but additional genetic or environmental factors are required to induce immune deficiency.
Clinical implications
Additional causes of this common immune deficiency syndrome remain to be determined.
Key words: Common variable immune deficiency, TACI, B cell, IgG, IgA, immune thrombocytopenia purpura, splenectomy
Abbreviations used: AIHA, Autoimmune hemolytic anemia, APRIL, A proliferation inducing ligand, BAFF, B cell–activating factor, CFSE, Carboxyfluorescein succinimidyl ester, CVID, Common variable immunodeficiency, ITP, Immune thrombocytopenia purpura, TACI, Transmembrane activator and calcium-modulating cyclophilin ligand interactor
Supported by grants from the National Institutes of Health (AI 101093, AI-467320, AI-48693) and National Institute of Allergy and Infectious Diseases Contract 03-22; and U19 AI0167152 and AR043274 to T.W.B. and N01-AI-30070 to B.G.
Disclosure of potential conflict of interest: C. Cunningham-Rundles is on advisory boards for OMRIX and Talacris and has received grants/research support from the National Institutes of Health. T. W. Behrens is an employee of Genentech. B. Grimbacher has received grants/research support from DFG, USIDnet, and the European Union. J. Bussel is on advisory boards for Amgen, GlaxoSmithKline, and Baxter; has stock or other equity ownership in Amgen and GlaxoSmithKline; has received grants/research support from Amgen, Biogen-IDEC, Cangene, Genentech, GlaxoSmithKline, and Sysmex; and is on the speakers' bureau for Baxter. The rest of the authors have declared that they have no conflict of interest.
PII: S0091-6749(07)01844-1
doi:10.1016/j.jaci.2007.10.001
© 2007 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
Volume 120, Issue 5 , Pages 1178-1185, November 2007
