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在人体中使用环孢素A抑制宿主反应的重复抗肿瘤抗体疗法。

Repeated antitumour antibody therapy in man with suppression of the host response by cyclosporin A.

作者信息

Ledermann J A, Begent R H, Bagshawe K D, Riggs S J, Searle F, Glaser M G, Green A J, Dale R G

机构信息

Department of Medical Oncology, Charing Cross Hospital, London, UK.

出版信息

Br J Cancer. 1988 Nov;58(5):654-7. doi: 10.1038/bjc.1988.279.

Abstract

Antibody targeted therapy of cancer results in anti-antibody production which prevents repeated treatment. Cyclosporin A (CsA) has been used to suppress this response in patients treated with a radiolabelled antibody to carcinoembryonic antigen (CEA). Patients with CEA producing tumours received a minimum of two courses consisting of an injection of radiolabelled antibody and CsA, 24 mg kg-1 day-1, for 6 days; each course was given at 2 week intervals. Two weeks after the completion of the second course the mean human antimouse antibody (HAMA) levels were 3.5 micrograms ml-1 (s.d. 2.7) in 3 patients receiving CsA and 1,998 micrograms ml-1 (s.d. 387) in 3 patients not receiving the drug. Clearance of antitumour antibody was accelerated and tumour localisation absent when HAMA levels exceeded 30 micrograms ml-1. With lower levels of HAMA in the CsA-treated patients, further antitumour antibody accumulated in the tumour after each dose. Further therapy with antitumour antibody and CsA lead to the development of HAMA, but this was less than 25% of the amount in patients not given CsA. In this preliminary study up to 4 times as many doses of antitumour antibody could be usefully given when CsA was used. This increases the potential for effective antibody targeted therapy of cancer.

摘要

癌症的抗体靶向治疗会引发抗抗体产生,从而阻碍重复治疗。环孢素A(CsA)已被用于抑制接受放射性标记癌胚抗原(CEA)抗体治疗患者的这种反应。患有产生CEA肿瘤的患者至少接受两个疗程的治疗,每个疗程包括注射放射性标记抗体和24毫克/千克/天的CsA,持续6天;每个疗程间隔2周进行。在完成第二个疗程两周后,3名接受CsA治疗的患者的平均人抗鼠抗体(HAMA)水平为3.5微克/毫升(标准差2.7),而3名未接受该药物治疗的患者的平均HAMA水平为1998微克/毫升(标准差387)。当HAMA水平超过30微克/毫升时,抗肿瘤抗体的清除加速且肿瘤定位消失。在接受CsA治疗的患者中,由于HAMA水平较低,每次给药后肿瘤中会积累更多的抗肿瘤抗体。用抗肿瘤抗体和CsA进行进一步治疗会导致HAMA产生,但这不到未给予CsA患者体内HAMA量的25%。在这项初步研究中,使用CsA时,抗肿瘤抗体的给药剂量最多可以增加到四倍。这增加了癌症有效抗体靶向治疗的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea98/2246821/3f8fa616d90b/brjcancer00133-0110-a.jpg

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