Perez R, Padavic K, Krigel R, Weiner L
Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
Cancer. 1991 May 15;67(10):2512-7. doi: 10.1002/1097-0142(19910515)67:10<2512::aid-cncr2820671021>3.0.co;2-5.
The cardiovascular, renal, pulmonary, and dermatologic toxicities of interleukin-2 (IL-2) and gamma-interferon (IFN) are well described. However, autoimmune toxicities have only recently been noticed. The authors report the development of warm autoantibodies against erythrocytes in a patient receiving IL-2 (3.75 x 10(6) cetus units/m2 intravenous bolus three times per week) and gamma-IFN (0.1 mg/m2 subcutaneously three times per week) for metastatic renal cell carcinoma. Other potential causes of autoantibody formation, such as drugs, infection, and collagen vascular disease, were excluded. Both gamma-IFN and IL-2 have the potential to trigger or exacerbate autoimmunity due to either aberrant expression of restricted antigens or inhibition of normal cellular immune suppressor mechanisms.
白细胞介素-2(IL-2)和γ-干扰素(IFN)的心血管、肾脏、肺部及皮肤毒性已有详细描述。然而,自身免疫毒性直到最近才被发现。作者报告了一名转移性肾细胞癌患者在接受IL-2(3.75×10⁶西图斯单位/平方米静脉推注,每周3次)和γ-IFN(0.1毫克/平方米皮下注射,每周3次)治疗时出现了抗红细胞温抗体。其他可能导致自身抗体形成的原因,如药物、感染和胶原血管病,均被排除。γ-IFN和IL-2都有可能由于受限抗原的异常表达或正常细胞免疫抑制机制的抑制而引发或加剧自身免疫。