Savage P, So A, Spooner R A, Epenetos A A
Department of Clinical Oncology, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.
Br J Cancer. 1993 Feb;67(2):304-10. doi: 10.1038/bjc.1993.57.
Recombinant interleukin-2 (rIL-2) therapy has been shown to be of value in the treatment of some cases of melanoma and renal cell carcinoma. However its use can be limited by severe systemic toxicity. Targeting rIL-2 to the tumour should improve the anti-tumour immune response and decrease the systemic toxicity. With this aim we have employed recombinant DNA techniques to construct a single chain antibody interleukin-2 fusion protein (SCA-IL-2). The protein used in this model system comprises the variable domains of the anti-lysozyme antibody D1.3 fused to human IL-2. It has been expressed by secretion from Escherichia coli and the purified product possesses antigen binding specificity and retains the immunostimulatory activities of rIL-2. This approach can be taken to generate SCA-IL-2 proteins that bind to appropriate cellular antigens. In vivo administration of a tumour binding SCA-IL-2 should result in a localised high concentration of IL-2 in tumour tissues, maximising the anti-tumour immune response, whilst keeping systemic side effects to a minimum.
重组白细胞介素-2(rIL-2)疗法已被证明在治疗某些黑色素瘤和肾细胞癌病例中具有价值。然而,其应用可能受到严重全身毒性的限制。将rIL-2靶向肿瘤应能改善抗肿瘤免疫反应并降低全身毒性。出于这一目的,我们采用重组DNA技术构建了一种单链抗体白细胞介素-2融合蛋白(SCA-IL-2)。该模型系统中使用的蛋白质包含与人IL-2融合的抗溶菌酶抗体D1.3的可变区。它通过大肠杆菌分泌表达,纯化产物具有抗原结合特异性,并保留了rIL-2的免疫刺激活性。可以采用这种方法来生成与适当细胞抗原结合的SCA-IL-2蛋白。在体内给予肿瘤结合性SCA-IL-2应能在肿瘤组织中产生局部高浓度的IL-2,最大限度地提高抗肿瘤免疫反应,同时将全身副作用降至最低。