Therapeutic window of MuS110, a single-chain antibody construct bispecific for murine EpCAM and murine CD3

被引:67
作者
Amann, Maria
Brischwein, Klaus
Lutterbuese, Petra
Parr, Larissa
Petersen, Laetitia
Lorenczewski, Grit
Krinner, Eva
Bruckmeier, Sandra
Lippold, Sandra
Kischel, Roman
Lutterbuese, Ralf
Kufer, Peter
Baeuerle, Patrick A.
Schlereth, Bernd
机构
[1] Micromet AG, Munich, Germany
[2] Micromet Inc, Bethesda, MD USA
关键词
D O I
10.1158/0008-5472.CAN-07-2182
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
EpCAM (CD326) is one of the most frequently and highly expressed tumor-associated antigens known and recently has also been found on cancer stem cells derived from human breast, colon, prostate, and pancreas tumors. However, like many other tumor-associated antigens used for antibody-based immunotherapeutic approaches, EpCAM is expressed on normal tissues including epithelia of pancreas, colon, lung, bile ducts, and breast. To assess the therapeutic window of an EpCAM/CD3-bispecific single-chain antibody construct of the bispecific T-cell engager (BiTE) class, we constructed murine surrogate of MT110 (muS110) from single-chain antibodies specific for murine EpCAM and CD3 antigens. Immunhistochemical analysis showed that, with minor differences, the expression of EpCAM protein on a large variety of tissues from man and mouse was similar with respect to distribution and level. MuS110 exhibited significant antitumor activity at as low as 5 mu g/kg in both syngeneic 4T1 orthotopic breast cancer and CT-26 lung cancer mouse models. Dosing of muS110 for several weeks up to 400 mu g/kg by intraanimal dose escalation was still tolerated, indicating existence of a significant therapeutic window for an EpCAM-specific BiTE antibody in mice. MuS110 was found to have similar in vitro characteristics and in vivo antitumor activity as MT110, a human EpCAM/human CD3-bispecific BiTE antibody that currently is in formal preclinical development.
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页码:143 / 151
页数:9
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