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. 2021 Apr 23;12:678927. doi: 10.3389/fimmu.2021.678927

Table 1.

Summary of the demographics, genetic and clinical characteristics, bone marrow examination, and treatment response of the VEXAS patients.

Patient 1 Patient 2
Demographic/genetic
Age of onset 69 75
UBA1 mutation p.Met41Thr p.Met41Leu
Clinical spectrum and laboratory findings at presentation
Hematopoietic Normocytic anemia Macrocytic anemia
Leukopenia Polyclonal hypergammaglobulinemia
Lymphopenia
Thrombopenia
Lymphoproliferation Cervical lymphadenopathy
Splenomegaly
Constitutional Fever Fever
Fatigue Fatigue
Weight loss Weight loss
Night sweats
Raised inflammatory markers Raised inflammatory markers
Hyperferritinemia Hyperferritinemia
Mucocutaneous Panniculitis-like nodular lesions Urticarial vasculitis
Livedo reticularis
Severe skin reaction to anakinra
Ophthalmologic Episcleritis Episcleritis
Musculoskeletal Arthralgia Symmetric polyarthritis
Nose chondritis Ear chondritis
Nose chondritis
Other Thrombophlebitis Deep venous thrombosis
MAS/HLH Pulmonary embolism
Bone marrow examination Moderately cellular Normocellular
Myeloid vacuolization and dysplasia Myeloid vacuolization and dysplasia
Dyserythropoiesis Dyserythropoiesis
Micromegakaryocytes Atypical plasmocytes
Hemophagocytosis (CD68 +) Plasmocytosis (6%)
MDS
Criteria/type Not evaluable due to folic acid deficiency No
Karyotype 46, XY[10] 46, XY[10]
NGS DNMT3A (c.1014+1G>T) VAF 31-46% Negative
Treatment (response)
Corticosteroids* Prednisone 60mg (+) Prednisolone 10mg (+)
Anti-TNF Infliximab (-)
Anti-IL-1 Anakinra (-)
Anti-IL-6 Siltuximab (+)
Other Rituximab (-) Methotrexate (-)
Sirolimus (+) Leflunomide (-)
Colchicine (-)

*Minimal dose with clinical response; +, clinical response; -, no clinical response; HLH, hemophagocytic lymphohistiocytosis; MAS, macrophage activation syndrome; MDS,myelodysplastic syndrome; NGS, next generation sequencing.