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Fatal CTLA‐4 heterozygosity with autoimmunity and recurrent infections: a de novo mutation

Primary immunodeficiency disorders are rarely diagnosed in adults but must be considered in the differential diagnosis of combined recurrent infections and autoimmune disease. We describe a patient with CTLA‐4 haploinsufficiency and an abnormal regulatory T‐cell phenotype. Unusually, infections were...

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Detalles Bibliográficos
Autores principales: Moraes‐Fontes, Maria Francisca, Hsu, Amy P., Caramalho, Iris, Martins, Catarina, Araújo, Ana Carolina, Lourenço, Filipa, Taulaigo, Anna V., Lladó, Ana, Holland, Steven M., Uzel, Gulbu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715409/
https://www.ncbi.nlm.nih.gov/pubmed/29225858
http://dx.doi.org/10.1002/ccr3.1257
Descripción
Sumario:Primary immunodeficiency disorders are rarely diagnosed in adults but must be considered in the differential diagnosis of combined recurrent infections and autoimmune disease. We describe a patient with CTLA‐4 haploinsufficiency and an abnormal regulatory T‐cell phenotype. Unusually, infections were more severe than autoimmunity, illustrating therapeutic challenges in disease course.