Kong Benjamin Y, Micklethwaite Kenneth P, Swaminathan Sanjay, Kefford Richard F, Carlino Matteo S
aCrown Princess Mary Cancer Centre bBlood and Marrow Transplant Service, Department of Haematology cDepartment of Clinical Immunology and Allergy, Westmead Hospital dFaculty of Medicine, The University of Sydney eMelanoma Institute Australia fFaculty of Medicine and Health Sciences, Macquarie University, Sydney, New South Wales, Australia.
Melanoma Res. 2016 Apr;26(2):202-4. doi: 10.1097/CMR.0000000000000232.
We report the occurrence of autoimmune hemolytic anemia in a patient receiving the anti-PD-1 monoclonal antibody, nivolumab, for metastatic melanoma in the presence of known red cell alloantibodies, despite having received prior ipilimumab without evidence of hemolysis. The patient had a history of multiple red cell alloantibodies and a positive direct antiglobulin test, identified at the time of a prior transfusion, which occurred before treatment with ipilimumab. The patient developed symptomatic warm autoimmune hemolytic anemia after four cycles of treatment with nivolumab. Clinical improvement was noted following cessation of the drug and treatment with corticosteroids. Given that there was no prior history of hemolysis, even during treatment with ipilimumab, we hypothesize that anti-PD-1 therapy disrupted peripheral tolerance, unmasking an underlying autoimmune predisposition.
我们报告了一名接受抗PD-1单克隆抗体纳武单抗治疗转移性黑色素瘤的患者发生自身免疫性溶血性贫血的情况,该患者存在已知的红细胞同种抗体,尽管之前接受过伊匹单抗治疗且无溶血证据。该患者有多种红细胞同种抗体病史,在伊匹单抗治疗前的一次输血时发现直接抗球蛋白试验呈阳性。该患者在接受四个周期的纳武单抗治疗后出现有症状的温抗体型自身免疫性溶血性贫血。停药并使用皮质类固醇治疗后临床症状改善。鉴于即使在伊匹单抗治疗期间也无溶血既往史,我们推测抗PD-1治疗破坏了外周耐受性,从而暴露了潜在的自身免疫易感性。