Schroff R W, Woodhouse C S, Foon K A, Oldham R K, Farrell M M, Klein R A, Morgan A C
J Natl Cancer Inst. 1985 Feb;74(2):299-306.
Antibody localization at the tumor site was assessed in melanoma patients who received the murine monoclonal antibody 9.2.27. Antibody was administered twice weekly in escalating doses from 1 to 500 mg. Localization was assessed by biopsies of cutaneous and lymph node lesions obtained 24-96 hours following therapy. The percentage of tumor cells that bound the antibody in vivo was dose dependent, with similar findings obtained by either flow cytometry or immunoperoxidase staining techniques. Little or no in vivo binding of the 9.2.27 antibody to tumor cells was found following 1- and 10-mg doses, whereas all specimens demonstrated in vivo binding of the antibody following 200- and 500-mg doses. Fluorescence staining intensity, as quantitated by flow cytometry, was employed to determine the degree of in vivo saturation of antibody binding sites following therapy. The degree of saturation was found to vary substantially among patients: Some patients demonstrated nearly 100% saturation after 200-mg doses of 9.2.27 antibody, whereas others demonstrated only half maximal saturation after doses of 500 mg. Although immunoperoxidase staining provided important qualitative information regarding the distribution of antigen and antibody within the tumor, these studies demonstrated the usefulness of immunofluorescent flow cytometry for quantitative assessment of antibody localization in solid tumors and provided information necessary for the design of further trials of monoclonal antibodies and immunoconjugates.
在接受鼠单克隆抗体9.2.27治疗的黑色素瘤患者中评估抗体在肿瘤部位的定位情况。抗体每周给药两次,剂量从1毫克递增至500毫克。在治疗后24至96小时获取皮肤和淋巴结病变的活检样本,以此评估定位情况。体内与抗体结合的肿瘤细胞百分比呈剂量依赖性,通过流式细胞术或免疫过氧化物酶染色技术均可得到类似结果。1毫克和10毫克剂量给药后,几乎未发现或仅发现极少的9.2.27抗体在体内与肿瘤细胞结合,而200毫克和500毫克剂量给药后的所有样本均显示抗体在体内与肿瘤细胞结合。通过流式细胞术定量的荧光染色强度,用于确定治疗后抗体结合位点的体内饱和程度。结果发现,不同患者之间饱和程度差异很大:一些患者在给予200毫克9.2.27抗体后显示接近100%的饱和,而另一些患者在给予500毫克剂量后仅显示出最大饱和程度的一半。虽然免疫过氧化物酶染色提供了有关肿瘤内抗原和抗体分布的重要定性信息,但这些研究证明了免疫荧光流式细胞术在定量评估实体瘤中抗体定位方面的实用性,并为进一步开展单克隆抗体和免疫缀合物试验设计提供了必要信息。