Bruton J K, Koeller J M
M.D. Anderson Cancer Center, Houston, Texas.
Pharmacotherapy. 1994 Nov-Dec;14(6):635-56.
Recombinant interleukin (IL)-2 is a newly approved immunoregulatory protein produced by lymphocytes that exhibits a wide range of immunologic effects. It is a true biologic response modifier in that is has no known direct antitumor activity, but mediates its cytotoxicity through activation of effector cells including T cells, natural killer cells, and lymphokine-activated killer cells. Recombinant IL-2 has demonstrated activity in patients with renal cell carcinoma and melanoma, with objective response rates of approximately 15-20%. The median duration of response in renal cell carcinoma is 23 months. Toxicity experienced with high-dose IL-2 can be significant. The most common dose-limiting toxicities are hypertension, weight gain, oliguria, respiratory insufficiency, and neurotoxicity. These effects are generally manageable and reversible on discontinuation of therapy. Administration of low-dose IL-2 has emerged as a means of substantially reducing toxicity. At least in renal cell carcinoma, it appears that the response rate to low-dose IL-2 is comparable to that with higher dosages.
重组白细胞介素(IL)-2是一种新批准的由淋巴细胞产生的免疫调节蛋白,具有广泛的免疫效应。它是一种真正的生物反应调节剂,因为它没有已知的直接抗肿瘤活性,而是通过激活包括T细胞、自然杀伤细胞和淋巴因子激活的杀伤细胞等效应细胞来介导其细胞毒性。重组IL-2已在肾细胞癌和黑色素瘤患者中显示出活性,客观缓解率约为15%-20%。肾细胞癌的中位缓解持续时间为23个月。高剂量IL-2所经历的毒性可能很显著。最常见的剂量限制性毒性是高血压、体重增加、少尿、呼吸功能不全和神经毒性。这些效应通常在停药后是可控且可逆的。低剂量IL-2的给药已成为大幅降低毒性的一种方法。至少在肾细胞癌中,低剂量IL-2的缓解率似乎与高剂量相当。