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Paediatric autoimmune diseases with ELANE mutations associated with neutropenia.
Zhang, Dan; Su, Gaixiu; Hao, Sheng; Lai, Jianming; Feng, Shunqiao.
Affiliation
  • Zhang D; Department of Rheumatology and Immunology, Capital Institute of Pediatrics, 2 Yabao Road, Chaoyang District, Beijing, China.
  • Su G; Department of Rheumatology and Immunology, Capital Institute of Pediatrics, 2 Yabao Road, Chaoyang District, Beijing, China. sugaixiucn@163.com.
  • Hao S; Department of Nephrology, Rheumatology and Immunology, Children's Hospital of Shanghai (also known as Children's Hospital, Shanghai Jiao Tong University School of Medicine), Shanghai, China. haos@shchildren.com.cn.
  • Lai J; Department of Rheumatology and Immunology, Capital Institute of Pediatrics, 2 Yabao Road, Chaoyang District, Beijing, China.
  • Feng S; Department of Hematopathology, Capital Institute of Pediatrics, Beijing, China.
Pediatr Rheumatol Online J ; 21(1): 41, 2023 Apr 28.
Article in En | MEDLINE | ID: mdl-37118811
ABSTRACT

OBJECTIVE:

To explore the clinical characteristics of autoimmune diseases in children with ELANE mutations.

METHODS:

Three cases of children with ELANE mutations manifesting as autoimmune diseases, who were under treatment from April 2020 to May 2021, were retrospectively analysed.

RESULTS:

Among the three children, two were boys aged 15 years and 22 months (cases 1 and 3) respectively, and the other one was a 22-month-old girl (case 2). All the cases had recurrent infections. Case 1 presented with cyclic neutropenia and systemic lupus erythematosus (SLE). Case 2 presented with severe neutropenia and autoimmune haemolytic anaemia (AHIA). Case 3 presented with severe neutropenia and anti-neutrophil cytoplasm antibodies (ANCA)-associated small vasculitis. Genetic tests showed that they all had heterozygous mutations in the ELANE gene. Case 1 was treated with methylprednisolone and hydroxychloroquine sulphate for 2 years, making neutrophil level return to normal. Case 2 received allogeneic hematopoietic stem cell transplantation and has stopped taking antibiotics, steroids and all the immunosuppressors. Case 3 received subcutaneous injections of granulocyte colony-stimulating factor, oral prednisone and cyclophosphamide. The boy in case 3 has been followed up for one year, and his absolute neutrophil count has increased to 1.56 × 109/L.

CONCLUSION:

Patients with ELANE mutations, combined with autoimmune diseases, may have recurrent infections. Disease-modifying antirheumatic drugs (DMARDs) are effective for autoimmune diseases. Autoimmune diseases with ELANE mutations associated with neutropenia can be cured through allogeneic hematopoietic stem cell transplantation.
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Full text: 1 Database: MEDLINE Main subject: Autoimmune Diseases / Neutropenia Type of study: Observational_studies / Risk_factors_studies Limits: Child / Female / Humans / Infant / Male Language: En Journal: Pediatr Rheumatol Online J Year: 2023 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Main subject: Autoimmune Diseases / Neutropenia Type of study: Observational_studies / Risk_factors_studies Limits: Child / Female / Humans / Infant / Male Language: En Journal: Pediatr Rheumatol Online J Year: 2023 Type: Article Affiliation country: China