Loutfi I, Batchelor J R, Lavender J P, Epenetos A A
Department of Immunology, Radiology and Clinical Oncology, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.
Int J Cancer Suppl. 1988;2:45-9.
In vitro tests were conducted using human T and B cell lines, as well as whole blood, to establish the usefulness of 2 murine monoclonal antibodies (MAbs), an anti-CD5 (Pan T) and a Pan B, for potential radioimmunolocalization and therapy. Both MAbs showed specificity for the cell line in question as tested by indirect immunofluorescence and radioimmunoassay. Assays carried out on whole blood showed 40-70% of the added activity of 111In-labelled Pan B antibody binding to B cells and 20-24% of 111In-Pan T antibody binding to T cells. The amount of internalised 111In-labelled Pan B was 6% of total amount at 24 hr indicating a slow internalisation process. These results should allow for in vivo targeting of normal and neoplastic B and T cells.
利用人T细胞系、B细胞系以及全血进行了体外试验,以确定两种鼠单克隆抗体(MAb)——一种抗CD5(泛T)抗体和一种泛B抗体——在潜在放射免疫定位和治疗方面的效用。通过间接免疫荧光和放射免疫测定法检测,两种单克隆抗体均对相关细胞系表现出特异性。对全血进行的检测显示,添加的铟-111标记泛B抗体有40%-70%与B细胞结合,铟-111标记泛T抗体有20%-24%与T细胞结合。24小时时,内化的铟-111标记泛B的量占总量的6%,表明内化过程缓慢。这些结果应有助于对正常和肿瘤性B细胞及T细胞进行体内靶向治疗。