Heterozygosity for transmembrane activator and calcium modulator ligand interactor A144E causes haploinsufficiency and pneumococcal susceptibility in mice

The B-cell receptor transmembrane activator and calcium modulator ligand interactor (TACI) is important for T-independent antibody responses. One in 200 blood donors are heterozygous for the TACI A181E mutation. We sought to investigate the effect on B-cell function of TACI A181E heterozygosity in r...

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Published inJournal of allergy and clinical immunology Vol. 139; no. 4; pp. 1293 - 1301.e4
Main Authors Jabara, Haifa H., Lee, John J., Janssen, Erin, Ullas, Sumana, Liadaki, Kyriaki, Garibyan, Lilit, Benson, Halli, Sannikova, Tatyana, Bram, Richard, Hammarstrom, Lennart, Cruz, Anthony C., Siegel, Richard, Manis, John, Malley, Richard, Geha, Raif S.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.04.2017
Elsevier Limited
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ISSN0091-6749
1097-6825
1085-8725
1097-6825
DOI10.1016/j.jaci.2016.07.028

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Summary:The B-cell receptor transmembrane activator and calcium modulator ligand interactor (TACI) is important for T-independent antibody responses. One in 200 blood donors are heterozygous for the TACI A181E mutation. We sought to investigate the effect on B-cell function of TACI A181E heterozygosity in reportedly healthy subjects and of the corresponding TACI A144E mutation in mice. Nuclear factor κB (NF-κB) activation was measured by using the luciferase assay in 293T cells cotransfected with wild-type and mutant TACI. TACI-driven proliferation, isotype switching, and antibody responses were measured in B cells from heterozygous TACI A144E knock-in mice. Mouse mortality was monitored after intranasal pneumococcal challenge. Levels of natural antibodies to the pneumococcal polysaccharide component phosphocholine were significantly lower in A181E-heterozygous than TACI-sufficient Swedish blood donors never immunized with pneumococcal antigens. Although overexpressed hTACI A181E and mTACI A144E acted as dominant-negative mutations in transfectants, homozygosity for A144E in mice resulted in absent TACI expression in B cells, indicating that the mutant protein is unstable when naturally expressed. A144E heterozygous mice, such as TACI+/− mice, expressed half the normal level of TACI on their B cells and exhibited similar defects in a proliferation-inducing ligand–driven B-cell activation, antibody responses to TNP-Ficoll, production of natural antibodies to phosphocholine, and survival after intranasal pneumococcal challenge. These results suggest that TACI A181E heterozygosity results in TACI haploinsufficiency with increased susceptibility to pneumococcal infection. This has important implications for asymptomatic TACI A181E carriers.
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ISSN:0091-6749
1097-6825
1085-8725
1097-6825
DOI:10.1016/j.jaci.2016.07.028