Yamamoto T, Yoneda K, Osaki T, Yoshimura N, Akagi N
Department of Radiology and Nuclear Medicine, Kochi Medical School, Japan.
Clin Exp Immunol. 1995 Apr;100(1):13-20. doi: 10.1111/j.1365-2249.1995.tb03597.x.
The local retention of adoptively transferred lymphokine (IL-2)-activated killer (LAK) cells was examined in 11 patients with head and neck carcinoma. Unseparated lymphocytes, T and natural killer (NK) cells isolated from patients were cultured with IL-2 for 7 days, labelled with 99mTc-HMPAO, and immediately injected back into the respective donors via the superficial temporal artery or locally into the tumour tissue. The injected LAK cells were periodically traced using a gamma camera, and the LAK cell retention rate was calculated from the radioactivity. One hour after the injection, about 70% of the locally infiltrated LAK cells remained in the tumour tissue, while about half of the LAK cells transferred via the regional artery were dislodged from the tissue. LAK cells induced from T cells (T-LAK) were retained in the tissue for a longer time than LAK cells induced from NK cells (NK-LAK). T-LAK were less chemotactic and less adherent to human umbilical vein endothelial cells (EC), and showed lesser migration through EC. Flow cytometric analysis revealed higher expression of CD11a, CD11b, CD18 and CD49d on NK-LAK compared with T-LAK. MoAbs against these adhesion molecules suppressed adhesion and migration of LAK cells. These results indicate that the rapid disappearance of NK-LAK from the tissue is associated with their greater chemotactic and adhesive as well as migratory activities depending on differing expression of adhesion molecules.
对11例头颈部癌患者进行了过继转移的淋巴因子(白细胞介素-2)激活的杀伤细胞(LAK细胞)的局部留存情况研究。从未分离的淋巴细胞、从患者体内分离出的T细胞和自然杀伤(NK)细胞与白细胞介素-2一起培养7天,用99mTc-HMPAO标记,然后立即通过颞浅动脉回注到各自的供体体内,或局部注入肿瘤组织。用γ相机定期追踪注入的LAK细胞,并根据放射性计算LAK细胞留存率。注射后1小时,局部浸润的LAK细胞约70%仍留在肿瘤组织中,而经区域动脉转移的LAK细胞约一半从组织中消失。由T细胞诱导产生的LAK细胞(T-LAK)在组织中的留存时间比由NK细胞诱导产生的LAK细胞(NK-LAK)更长。T-LAK的趋化性和对人脐静脉内皮细胞(EC)的黏附性较低,穿过EC的迁移能力也较弱。流式细胞术分析显示,与T-LAK相比,NK-LAK上CD11a、CD11b、CD18和CD49d的表达更高。针对这些黏附分子的单克隆抗体抑制了LAK细胞的黏附和迁移。这些结果表明,NK-LAK从组织中的快速消失与其更强的趋化性、黏附性以及迁移活性有关,这取决于黏附分子的不同表达。