Department of Pediatrics, Division of Hematology/Oncology, University of Michigan, Ann Arbor, MI, United States.
Department of Pharmacy, University of Michigan, Ann Arbor, MI, United States.
Front Immunol. 2022 Apr 19;13:863177. doi: 10.3389/fimmu.2022.863177. eCollection 2022.
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.
难治性免疫性血小板减少症的治疗常涉及利妥昔单抗,一种嵌合抗 CD20 单克隆抗体,以靶向 B 细胞并诱导大多数患者缓解。然而,中和利妥昔单抗治疗反应并可能导致血清病的抗体很少有报道。在这里,我们报告了一例年轻成年女性 Evans 综合征患者接受利妥昔单抗治疗,并发血清病、急性呼吸窘迫综合征和血小板难治性,推测与抗利妥昔单抗的中和抗体有关。她成功地接受了人源化抗 CD20 单克隆抗体奥滨尤妥珠单抗治疗,随后症状缓解。此外,还对之前发表的 10 例与利妥昔单抗治疗特发性血小板减少性紫癜(ITP)相关的血清病病例进行了综述。本病例强调,认识到利妥昔单抗诱导的血清病更微妙或罕见的症状对于促进快速干预非常重要。