Harning R, Myers C, Merluzzi V J
Roberts Pharmaceutical Corporation, Research and Development Eatontown, NJ 07724.
Clin Exp Metastasis. 1993 Jul;11(4):337-42. doi: 10.1007/BF00058054.
The leukocyte integrins are cell adhesion molecules which play pivotal roles in the development of a variety of immune responses including T-cell-mediated cytotoxicity, lymphocyte proliferation, macrophage presentation of antigen, and adhesion of leukocytes to vascular endothelium. The relevance of lymphocyte function-associated antigen-1 (LFA-1) to leukocyte malignancies is currently under examination in a number of laboratories. Here, we present evidence demonstrating that LFA-1 plays a role during the in vitro invasion of human endothelium by JY lymphoma cells and during in vivo metastasis of two distinct models of murine leukemia: P815 mastocytoma and EL4 lymphoma. When assayed in vitro, a murine anti-human LFA-1 (alpha subunit) monoclonal antibody (mAb) inhibits up to 80% of JY lymphoma cell invasion. When assayed in vivo, a rat anti-LFA-1 (alpha subunit) mAb significantly inhibited the development of experimental metastases, when administered concomitantly with either P815 or EL4 tumor cells. The leukocyte integrins, particularly LFA-1, may represent useful targets for the therapeutic modulation of metastasis.
白细胞整合素是细胞粘附分子,在多种免疫反应的发展中起关键作用,包括T细胞介导的细胞毒性、淋巴细胞增殖、巨噬细胞对抗原的呈递以及白细胞与血管内皮的粘附。淋巴细胞功能相关抗原-1(LFA-1)与白细胞恶性肿瘤的相关性目前正在多个实验室进行研究。在此,我们提供证据表明,LFA-1在JY淋巴瘤细胞体外侵袭人内皮细胞的过程中以及在两种不同的小鼠白血病模型(P815肥大细胞瘤和EL4淋巴瘤)的体内转移过程中发挥作用。在体外试验中,一种鼠抗人LFA-1(α亚基)单克隆抗体(mAb)可抑制高达80%的JY淋巴瘤细胞侵袭。在体内试验中,当与P815或EL4肿瘤细胞同时给药时,一种大鼠抗LFA-1(α亚基)mAb可显著抑制实验性转移的发生。白细胞整合素,尤其是LFA-1,可能是转移治疗调节的有用靶点。