Schroff R W, Farrell M M, Klein R A, Oldham R K, Foon K A
J Immunol. 1984 Sep;133(3):1641-8.
Antigenic modulation of the T65 cell surface antigen was assessed in chronic lymphocytic leukemia patients (CLL) receiving therapy with the murine monoclonal antibody T101 in a phase I clinical trial. A total of 12 patients received 1, 10, or 40 mg doses administered over 2 hr, or 50 or 100 mg doses administered over 50 hr. Decreases in T65 antigen expression (up to 90%) coincided with decreases in the circulating leukemic cell count in those patients who received T101 over a 2-hr period, indicating that clearance of circulating T65 antigen-positive cells could account for most of the observed decreases in T65 antigen expression. In contrast, analysis of bone marrow specimens from these patients indicated that decreases in T65 antigen density in this relatively stationary population resulted not from a cell decrement but rather from antigenic modulation. Pulmonary toxicity prevented administration of doses greater than 40 mg over a 2-hr period; therefore, higher doses (50 and 100 mg) were administered over a 50-hr period. This treatment schedule resulted in greater than 90% reduction in T65 antigen density of both circulating and bone marrow leukemic cells without dramatic drops in circulating leukemic cell counts, indicating that antigenic modulation accounted for most of the observed decreases in T65 antigen density under these conditions. Reexpression of T65 antigen by modulated cells was observed both in vitro and in vivo within 2 to 4 days. Immunoperoxidase staining of in vivo-modulated specimens and in vitro modulation studies with 125I-T101 suggested that T65 antigen-T101 antibody complexes were internalized during modulation. Although antigenic modulation inhibits the potential therapeutic effectiveness of unconjugated T101 antibody in CLL patients, treatment of CLL with T101 drug or toxin immunoconjugates under conditions that bring about rapid and extensive internalization of the T65 antigen may provide an effective means of therapy.
在一项I期临床试验中,对接受鼠单克隆抗体T101治疗的慢性淋巴细胞白血病患者(CLL)的T65细胞表面抗原的抗原调制情况进行了评估。共有12名患者接受了在2小时内给予的1毫克、10毫克或40毫克剂量,或在50小时内给予的50毫克或100毫克剂量。在那些在2小时内接受T101治疗的患者中,T65抗原表达的下降(高达90%)与循环白血病细胞计数的下降同时出现,这表明循环T65抗原阳性细胞的清除可解释观察到的T65抗原表达下降的大部分情况。相比之下,对这些患者骨髓标本的分析表明,在这个相对静止的群体中T65抗原密度的下降不是由于细胞数量减少,而是由于抗原调制。肺部毒性使得无法在2小时内给予超过40毫克的剂量;因此,更高的剂量(50毫克和100毫克)在50小时内给予。这种治疗方案导致循环和骨髓白血病细胞的T65抗原密度降低超过90%,而循环白血病细胞计数没有急剧下降,这表明在这些条件下,抗原调制是观察到的T65抗原密度下降的主要原因。在2至4天内,在体外和体内均观察到调制细胞重新表达T65抗原。体内调制标本的免疫过氧化物酶染色以及用125I-T101进行的体外调制研究表明,T65抗原-T101抗体复合物在调制过程中被内化。虽然抗原调制会抑制未结合的T101抗体在CLL患者中的潜在治疗效果,但在能导致T65抗原快速广泛内化的条件下,用T101药物或毒素免疫缀合物治疗CLL可能提供一种有效的治疗方法。