Case Report: Characterizing the Role of the STXBP2-R190C Monoallelic Mutation Found in a Patient With Hemophagocytic Syndrome and Langerhans Cell Histiocytosis


Por: Viñas-Giménez L, Rincón R, Colobran R, de la Cruz X, Celis-Passini V, Dapena JL, Alsina L, Sayós J and Martínez-Gallo M

Publicada: 23 sep 2021 Ahead of Print: 23 sep 2021
Resumen:
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory disorder. HLH can be considered as a threshold disease depending on the trigger and the residual NK-cell cytotoxicity. In this study, we analyzed the molecular and functional impact of a novel monoallelic mutation found in a patient with two episodes of HLH. A 9-month-old child was diagnosed at 2 months of age with cutaneous Langerhans cell histiocytosis (LCH). After successful treatment, the patient developed an HLH episode. At 16 month of age, the patient went through an HSCT losing the engraftment 5 months later concomitant with an HLH relapse. The genetic study revealed a monoallelic mutation in the STXBP2 gene (.pArg190Cys). We transfected COS7 cells to analyze the STXBP2-R190C expression and to test the interaction with STX11. We used the RBL-2H3 cell line expressing STXBP2-WT-EGFP or R190C-EGFP for degranulation assays. Mutation STXBP2-R190C did not affect protein expression or interaction with syntaxin-11. However, we have demonstrated that STXBP2-R190C mutation diminishes degranulation in the RBL-2H3 cell line compared with the RBL-2H3 cell line transfected with STXBP2-WT or nontransfected. These results suggest that STXBP2-R190C mutation acts as a modifier of the degranulation process producing a decrease in degranulation. Therefore, under homeostatic conditions, the presence of one copy of STXBP2-R190 could generate sufficient degranulation capacity. However, it is likely that early in life when adaptive immune system functions are not sufficiently developed, an infection may not be resolved with this genetic background, leading to a hyperinflammation syndrome and eventually develop HLH. This analysis highlights the need for functional testing of new mutations to validate their role in genetic susceptibility and to establish the best possible treatment for these patients.

Filiaciones:
Viñas-Giménez L:
 Immunology Division, Hospital Universitari Vall d'Hebron (HUVH), Jeffrey Model Foundation Excellence Center, Barcelona, Spain

 Diagnostic Immunology Research Group Vall d'Hebron Research Institute (VHIR), Barcelona, Spain

 Department of Cell Biology, Physiology and Immunology, Autonomous University of Barcelona (UAB), Barcelona, Spain

Rincón R:
 Immunology Division, Hospital Universitari Vall d'Hebron (HUVH), Jeffrey Model Foundation Excellence Center, Barcelona, Spain

Colobran R:
 Immunology Division, Hospital Universitari Vall d'Hebron (HUVH), Jeffrey Model Foundation Excellence Center, Barcelona, Spain

 Diagnostic Immunology Research Group Vall d'Hebron Research Institute (VHIR), Barcelona, Spain

 Department of Cell Biology, Physiology and Immunology, Autonomous University of Barcelona (UAB), Barcelona, Spain

 Genetics Department, Hospital UniversitariVall d'Hebron (HUVH), Barcelona, Spain

de la Cruz X:
 Research Unit in Translational Bioinformatics in Neurosciences, Universitat Autònoma de Barcelona, Barcelona, Spain

 Institut Catala per la Recerca i Estudis Avançats (ICREA), Barcelona, Spain

Celis-Passini V:
 Hematology Department, Pediatric Cancer Center, Hospital Sant Joan de Déu, Esplugues de Llobregat, Spain

Dapena JL:
 Hematology Department, Pediatric Cancer Center, Hospital Sant Joan de Déu, Esplugues de Llobregat, Spain

Alsina L:
 Clinical Immunology and Primary Immunodeficiencies Unit, Allergy and Clinical Immunology Department, Hospital Sant Joan de Déu, University of Barcelona, Pediatric Research Institute Sant Joan de Déu, Barcelona, Spain

Sayós J:
 Immune Regulation and Immunotherapy Group, CIBBIM-Nano medicine, Vall d'Hebron Institut de Recerca, Universitat Autonoma de Barcelona, Barcelona, Spain

Martínez-Gallo M:
 Immunology Division, Hospital Universitari Vall d'Hebron (HUVH), Jeffrey Model Foundation Excellence Center, Barcelona, Spain

 Diagnostic Immunology Research Group Vall d'Hebron Research Institute (VHIR), Barcelona, Spain

 Department of Cell Biology, Physiology and Immunology, Autonomous University of Barcelona (UAB), Barcelona, Spain
ISSN: 16643224





Frontiers in Immunology
Editorial
FRONTIERS MEDIA SA, AVENUE DU TRIBUNAL FEDERAL 34, LAUSANNE CH-1015, SWITZERLAND, Suiza
Tipo de documento: Article
Volumen: 12 Número:
Páginas: 723836-723836
WOS Id: 000704515100001
ID de PubMed: 34630398
imagen Green Submitted, gold

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