Autoinflammatory and immunodeficiency due to loss of function mutation in ELF4.

• Ortiz Ramírez, Ana ^[1] ; Blanco Lobo, Pilar ^[1] ; De Felipe, Bea ^[1] ; Moreno Fuentes, David ^[1] ; Olbrich, Peter ^[1] ; Neth, Olaf ^[1] ; Rodríguez, Alejandro ^[1]
  1. [1] Hospital Universitario Virgen del Rocío

     Hospital Universitario Virgen del Rocío

     Sevilla, España

     
• Localización: Biosaia: Revista de los másteres de Biotecnología Sanitaria y Biotecnología Ambiental, Industrial y Alimentaria, ISSN-e 2254-3821, Nº. 13, 2024
• Idioma: español
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• Resumen

  • Background: Inborn errors of immunity (IEI) are defined as monogenetic germline defects characterized by increasedsusceptibility to infections, immune diseases, allergies, and cancers. Recently, a new condition called "deficiency inELF4, X-linked" (DEX) has been identified as a disease of immune dysregulation [1]. DEX patients commonly manifestsymptoms such as fevers, along with various inflammatory manifestations that primarily affect the gastrointestinaltract, as well as notable involvement of the skin [2, 3]. Despite the identification of the condition and the involvementof the ELF4 gene, the specific biological processes and mechanisms by which DEX and ELF4 function results in theobserved symptoms are not completely understood. In addition, a personalized therapy is needed due to thecomplexity of the disease.Objective: Here, we aim to explore the link between ELF4 deficiency and the pro-inflammatory state resulting in theclinical manifestations of these patients. We also pursue to evaluate the ex vivo effects of JAK inhibition.Methods: Using flow cytometry, RT-qPCR and ELISA techniques, the levels of STAT1 and pSTAT1 were examined inIFN stimulated cells obtained from ELF4 deficient, STAT1 GOF patients and healthy controls. By using nCounterFLEX (NanoString) platform and Luminex assay, we quantified expression levels of IFN-response genes and serumcytokine levels.Results: ELF4 deficient and STAT1 GOF patients presented similar phenotype characterized by increased STAT1 andpSTAT1 levels in response to INFa and IFNg. STAT1-downstream gene expression and CXCL10 secretion wereelevated compare to healthy controls. Ex vivo treatment with Ruxolitinib (JAK1/2 inhibitor) reduced STAT1phosphorylation in ELF4 and STAT1 GOF patient cells.Conclusion: These results have improved the comprehension of ELF4 role in autoinflammatory syndromes. However,further investigations are required in order to fully understand the impact of ELF4 deficiency in immunedysregulation and the potential targeted therapies that could benefit those patients including JAK inhibitors.