Monoclonal Insulin Autoimmune Syndrome Successfully Treated With Plasma Cell Directed Therapy.

IF 2.7 4区 医学 Q2 HEMATOLOGY
Frida Bugge Askeland, Hege M Frøen, Nils Bolstad, Per Medbøe Thorsby, Fredrik Schjesvold, Anne Cathrine Parelius Wammer, Ivar Følling, Geir E Tjønnfjord
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引用次数: 0

Abstract

Background: Monoclonal insulin autoimmune syndrome (IAS) is a very rare disease characterized by severe attacks of hypoglycemia caused by circulating anti-insulin antibodies produced by a B-cell clone, usually clonal plasma cells.

Method: We present 2 female Norwegian patients with monoclonal IAS. The anti-insulin antibodies were quantified by immune precipitation and characterized using a 3-step manual in-house assay. Both patients received plasma cell directed therapy.

Result: The first patient received plasma cell directed therapy for a time-limited period and achieved a sustained clinical remission without detectable anti-insulin antibodies. The second patient receives continuous plasma cell directed therapy and is in clinical remission with low values of detectable anti-insulin antibodies.

Conclusion: Plasma cell directed therapy was effective and safe in our 2 cases of monoclonal IAS. We recommend considering plasma cell directed therapy for these patients.

利用血浆细胞导向疗法成功治疗单克隆胰岛素自身免疫综合征
背景:单克隆胰岛素自身免疫综合征(IAS单克隆胰岛素自身免疫综合征(IAS)是一种非常罕见的疾病,其特征是由B细胞克隆(通常是克隆浆细胞)产生的循环抗胰岛素抗体导致的严重低血糖发作:我们介绍了两名患有单克隆 IAS 的挪威女性患者。抗胰岛素抗体通过免疫沉淀法进行定量,并采用内部三步人工检测法进行鉴定。两名患者均接受了浆细胞导向疗法:结果:第一名患者接受了有时限的血浆细胞导向疗法,并获得了持续的临床缓解,没有检测到抗胰岛素抗体。第二名患者接受了持续的血浆细胞导向疗法,临床症状得到缓解,检测到的抗胰岛素抗体值较低:结论:浆细胞导向疗法对我们的 2 例单克隆 IAS 患者有效且安全。我们建议考虑对这些患者进行浆细胞导向疗法。
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来源期刊
CiteScore
2.70
自引率
3.70%
发文量
1606
审稿时长
26 days
期刊介绍: Clinical Lymphoma, Myeloma & Leukemia is a peer-reviewed monthly journal that publishes original articles describing various aspects of clinical and translational research of lymphoma, myeloma and leukemia. Clinical Lymphoma, Myeloma & Leukemia is devoted to articles on detection, diagnosis, prevention, and treatment of lymphoma, myeloma, leukemia and related disorders including macroglobulinemia, amyloidosis, and plasma-cell dyscrasias. The main emphasis is on recent scientific developments in all areas related to lymphoma, myeloma and leukemia. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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