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Phenotypic complementation of genetic immunodeficiency by chronic herpesvirus infection

Variation in the presentation of hereditary immunodeficiencies may be explained by genetic or environmental factors. Patients with mutations in HOIL1 (RBCK1) present with amylopectinosis-associated myopathy with or without hyper-inflammation and immunodeficiency. We report that barrier-raised HOIL-1...

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Detalles Bibliográficos
Autores principales: MacDuff, Donna A, Reese, Tiffany A, Kimmey, Jacqueline M, Weiss, Leslie A, Song, Christina, Zhang, Xin, Kambal, Amal, Duan, Erning, Carrero, Javier A, Boisson, Bertrand, Laplantine, Emmanuel, Israel, Alain, Picard, Capucine, Colonna, Marco, Edelson, Brian T, Sibley, L David, Stallings, Christina L, Casanova, Jean-Laurent, Iwai, Kazuhiro, Virgin, Herbert W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298697/
https://www.ncbi.nlm.nih.gov/pubmed/25599590
http://dx.doi.org/10.7554/eLife.04494