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在无原发性肿瘤的情况下,抗体优先靶向小的淋巴瘤转移灶。

Preferential antibody targeting to small lymphoma metastases in the absence of the primary tumour.

作者信息

Schmid U, Schirrmacher V, Momburg F, Matzku S

机构信息

Institut für Radiologie und Pathophysiologie, Krebsforschungszentrum, Heidelberg, F.R.G.

出版信息

Eur J Cancer. 1993;29A(2):217-25. doi: 10.1016/0959-8049(93)90179-j.

Abstract

Targeting of spontaneous liver metastases of the ESb.MP murine lymphoma was achieved with anti-CD2 monoclonal antibody (MAb) 12-15A, which does not react with normal liver tissue. Using quantitative autoradiography on whole body sections of animals that had received a standard dose of 1.1 MBq of 125I-labelled monoclonal antibody, metastases accumulated up to > 90% of the injected dose per gram (id/g). The average uptake of primary tumour lesions was at a low level of 24 Bq/mg (corresponding to 2.2% id/g) because of highly non-uniform accumulation, while metastatic lesions were all above 50 Bq/mg. Uptake was particularly pronounced in animals tested after resection of the primary tumour: 85% of metastases showed levels above 300 Bq/mg, which was the upper limit of uptake in metastases of non-resected animals. These findings demonstrate the potential of the antibody approach with regard to attacking residual metastatic lesions after debulking.

摘要

使用不与正常肝组织发生反应的抗CD2单克隆抗体(MAb)12 - 15A实现了对ESb.MP小鼠淋巴瘤自发性肝转移灶的靶向作用。对接受标准剂量1.1 MBq 125I标记单克隆抗体的动物全身切片进行定量放射自显影,转移灶每克累积摄取量高达注射剂量的90%以上(每克注射剂量,id/g)。由于累积高度不均匀,原发性肿瘤病灶的平均摄取量处于较低水平,为24 Bq/mg(相当于2.2% id/g),而转移病灶均高于50 Bq/mg。在原发性肿瘤切除后进行测试的动物中摄取尤为明显:85%的转移灶显示水平高于300 Bq/mg,这是非切除动物转移灶摄取的上限。这些发现证明了抗体方法在攻击减瘤后残留转移病灶方面的潜力。

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