Topalian S L, Rosenberg S A
Surgery Branch, National Cancer Institute, Bethesda, Md.
Acta Haematol. 1987;78 Suppl 1:75-6. doi: 10.1159/000205907.
A new approach to cancer treatment has been developed based on the adoptive transfer of activated lymphocytes into cancer patients. Lymphocytes harvested from patients by leukapheresis are converted into lymphokine-activated killer (LAK) cells by incubation with recombinant interleukin-2 (rIL-2). These LAK cells are then infused back into the patients in combination with intravenous IL-2. Among 25 patients treated with this form of adoptive immunotherapy there were 11 patients with measurable tumor reductions, including 1 complete responder. The majority of responses occurred in patients with metastatic renal cell carcinoma, melanoma and colorectal carcinoma. The toxicities of IL-2, including fluid retention and pulmonary edema, limit therapy, and laboratory investigation is now aimed toward understanding the mechanism of IL-2 toxicity. The use of LAK cells and IL-2 in cancer therapy is still in a developmental stage and needs to be refined before its role can be definitely established.
一种基于将活化淋巴细胞过继转移至癌症患者体内的癌症治疗新方法已被开发出来。通过白细胞分离术从患者体内采集的淋巴细胞,经与重组白细胞介素-2(rIL-2)孵育后转化为淋巴因子激活的杀伤细胞(LAK细胞)。然后,这些LAK细胞与静脉注射的IL-2联合回输到患者体内。在接受这种过继免疫疗法治疗的25例患者中,有11例患者的肿瘤体积出现了可测量的缩小,其中包括1例完全缓解者。大多数反应发生在转移性肾细胞癌、黑色素瘤和结直肠癌患者中。IL-2的毒性,包括液体潴留和肺水肿,限制了治疗,目前实验室研究旨在了解IL-2毒性的机制。LAK细胞和IL-2在癌症治疗中的应用仍处于发展阶段,在其作用能够明确确立之前,还需要进一步完善。