Artículo
Pediatric inborn errors of immunity causing hemophagocytic lymphohistiocytosis: Case report and review of the literature
Caldirola, Maria Soledad
; Gómez Raccio, Andrea Cecilia; Di Giovanni, Daniela; Gaillard, María Isabel; Preciado, María Victoria
Fecha de publicación:
07/2022
Editorial:
Federation of American Societies for Experimental Biology
Revista:
Journal of Leukocyte Biology
ISSN:
0741-5400
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
Inborn errors of immunity are a group of genetic disorders caused by mutations that affect the development and/or function of several compartments of the immune system, predisposing patients to infections, autoimmunity, allergy and malignancies. In this regard, mutations that affect proteins involved in trafficking, priming, docking, or membrane fusion will impair the exocytosis of lytic granules of effector NK and cytotoxic T lymphocytes. This may predispose patients to hemophagocytic lymphohistiocytosis, a life-threatening immune disorder characterized by systemic lymphocyte and macrophage activation, and increased levels of cytokines, which lead to an uncontrolled hyperinflammation state and progressive multiorgan damage. In this review, we will describe a clinical case and recent advances in inborn errors of immunity predisposing to hemophagocytic lymphohistiocytosis. Summary sentence: Review of recent advances in inborn errors of immunity predisposing to hemophagocytic lymphohistiocytosis.
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Articulos(IMIPP)
Articulos de INSTITUTO MULTIDISCIPLINARIO DE INVESTIGACIONES EN PATOLOGIAS PEDIATRICAS
Articulos de INSTITUTO MULTIDISCIPLINARIO DE INVESTIGACIONES EN PATOLOGIAS PEDIATRICAS
Citación
Caldirola, Maria Soledad; Gómez Raccio, Andrea Cecilia; Di Giovanni, Daniela; Gaillard, María Isabel; Preciado, María Victoria; Pediatric inborn errors of immunity causing hemophagocytic lymphohistiocytosis: Case report and review of the literature; Federation of American Societies for Experimental Biology; Journal of Leukocyte Biology; 112; 4; 7-2022; 607-615
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