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Re-evaluation of the contribution of TNFRSF13B variants to antibody deficiencyTNFRSF13B/TACI deficiency

The presence of a second TNFRSF13B mutation, HLA class II markers, or multiple single nucleotide variants in patients helps to explain the incomplete penetrance of immunodeficiency in carriers of TNFRSF13B mutations.

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Principais autores: Hassan Abolhassani, Andrés Caballero-Oteyza, Mingyu Yang, Michele Proietti, Samaneh Delavari, Patrick Maffucci, Alejandro A. Schäffer, Bertrand Boisson, Jean-Laurent Casanova, Nima Rezaei, Qiang Pan-Hammarström, Charlotte Cunningham-Rundles, Lennart Hammarström, Bodo Grimbacher
Formato: Artigo
Idioma:Inglês
Publicado em: Rockefeller University Press 2025-08-01
coleção:Journal of Human Immunity
Acesso em linha:https://rupress.org/jhi/article-pdf/doi/10.70962/jhi.20250016/1949050/jhi_20250016.pdf
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