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A Novel Complete Autosomal-Recessive STAT1 LOF Variant Causes Immunodeficiency with Hemophagocytic Lymphohistiocytosis-Like Hyperinflammation
- Source :
- The journal of allergy and clinical immunology. In practice. 8(9)
- Publication Year :
- 2020
-
Abstract
- Complete signal transducer and activator of transcription 1 (STAT1) deficiency causes a rare primary immunodeficiency that is characterized by defective IFN-dependent gene expression leading to life-threatening viral and mycobacterial infections early in life.To characterize a novel STAT1 loss-of-function variant leading to pathological infection susceptibility and hyperinflammation.Clinical, immunologic, and genetic characterization of a patient with severe infections and hemophagocytic lymphohistiocytosis-like hyperinflammation was investigated.We reported a child of consanguineous parents who presented with multiple severe viral infections that ultimately triggered hemophagocytic lymphohistiocytosis and liver failure. Despite intensified therapy with antivirals and cytomegalovirus-specific donor cells, the child died after hematopoietic stem cell transplantation because of cytomegalovirus reactivation with acute respiratory distress syndrome. Exome sequencing revealed a homozygous STAT1 variant (p.Val339ProfsTer18), leading to loss of STAT1 protein expression. Upon type I and type II IFN stimulation, immune and nonimmune cells showed defective upregulation of IFN-stimulated genes and increased susceptibility to viral infection in vitro. Increased viral infection rates were paralleled by hyperinflammatory ex vivo cytokine responses with increased production of TNF, IL-6, and IL-18.Complete STAT1 deficiency is a devastating disorder characterized by severe viral infections and ensuing hyperinflammatory responses. Early diagnosis can be made by exome sequencing and variant validation by functional testing of STAT1-dependent programmed cell death 1 ligand 1 surface expression on monocytes. Furthermore, high awareness for hyperinflammatory complications and potential targeted treatment strategies such as IL-18 binding protein could be considered. Hematopoietic stem cell transplantation is the only definitive treatment strategy but remains challenging.
- Subjects :
- medicine.medical_treatment
Cytomegalovirus
Hematopoietic stem cell transplantation
Lymphohistiocytosis, Hemophagocytic
03 medical and health sciences
0302 clinical medicine
Immune system
Interferon
medicine
Immunology and Allergy
CXCL10
Humans
030212 general & internal medicine
Child
Immunodeficiency
Exome sequencing
Hemophagocytic lymphohistiocytosis
business.industry
Hematopoietic Stem Cell Transplantation
Immunologic Deficiency Syndromes
medicine.disease
STAT1 Transcription Factor
030228 respiratory system
Virus Diseases
Immunology
Primary immunodeficiency
business
medicine.drug
Subjects
Details
- ISSN :
- 22132201
- Volume :
- 8
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- The journal of allergy and clinical immunology. In practice
- Accession number :
- edsair.doi.dedup.....fd2fe0c4d0698a4269d5639c94ec0a0d