Siber G R, Ambrosino D M, Gorgone B C
Ann Intern Med. 1982 May;96(5):580-6. doi: 10.7326/0003-4819-96-5-580.
A platelet transfusion from a blood group O donor, immunized 1 month before with Pneumovax, caused a hemolytic reaction in a blood group A recipient. Forty-five of 59 group O donors (76%) and all of nine group B donors immunized with Pneumovax had a fourfold or higher anti-A response. Half of the anti-A antibody in high titered donors was in the IgG fraction. Pneumovax contained approximately 30 micrograms of an A-like substance per dose; polyvalent pneumococcal vaccines prepared by two other manufactures contained very low and probably subimmunogenic concentrations. Several culture media prepared from animal tissues contained as antigen of similar physical, immunologic, and chemical properties, and were the most likely source of the contaminant. Manufacturing procedures have since been revised to eliminate A-like substances.
一名O型血供者在1个月前接种肺炎球菌疫苗后进行的血小板输注,导致一名A型血受者发生溶血反应。59名接种肺炎球菌疫苗的O型血供者中有45名(76%)以及所有9名B型血供者产生了四倍或更高的抗A反应。高滴度供者中一半的抗A抗体存在于IgG组分中。每剂肺炎球菌疫苗含有约30微克类似A物质;另外两家制造商生产的多价肺炎球菌疫苗含有极低且可能低于免疫原性的浓度。几种由动物组织制备的培养基含有具有相似物理、免疫和化学性质的抗原,是最可能的污染物来源。此后已修订生产程序以消除类似A物质。