美罗华
医学
奥比努图库单抗
CD20
免疫学
血小板减少性紫癜
耐火材料(行星科学)
血清病
单克隆抗体
抗体
单克隆
内科学
免疫系统
物理
天体生物学
作者
Jennifer R. Blase,David Frame,Thomas F. Michniacki,Kelly Walkovich
标识
DOI:10.3389/fimmu.2022.863177
摘要
Management of refractory immune thrombocytopenia frequently involves rituximab, a chimeric anti-CD20 monoclonal antibody, to target B cells and induce remission in most patients. However, neutralizing antibodies to rituximab that nullify therapeutic response and may lead to serum sickness have been rarely reported. Here, we present a case of a young adult woman with Evans syndrome treated with rituximab, complicated by the development of serum sickness, acute respiratory distress syndrome, and platelet refractoriness presumed secondary to neutralizing antibodies to rituximab. She was successfully treated with the humanized anti-CD20 monoclonal antibody, obinutuzumab, with subsequent symptom resolution. Additionally, a review of 10 previously published cases of serum-sickness associated with the use of rituximab for idiopathic thrombocytopenic purpura (ITP) is summarized. This case highlights that recognition of more subtle or rare symptoms of rituximab-induced serum sickness is important to facilitate rapid intervention.
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