Methods for site-specific drug conjugation to antibodies.

Methods for site-specific drug conjugation to antibodies.
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DOI:
10.4161/mabs.26632
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发表时间:
2014-01
期刊:
影响因子:
5.3
通讯作者:
Liu B
Liu B
中科院分区:
医学2区
文献类型:
--
作者:
Behrens CR;Liu B

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Antibody drug conjugates (ADCs) are an emerging class of targeted therapeutics with the potential to improve therapeutic index over traditional chemotherapy. Drugs and linkers have been the current focus of ADC development, in addition to antibody and target selection. Recently, however, the importance of conjugate homogeneity has been realized. The current methods for drug attachment lead to a heterogeneous mixture, and some populations of that mixture have poor in vivo performance. New methods for site-specific drug attachment lead to more homogeneous conjugates and allow control of the site of drug attachment. These subtle improvements can have profound effects on in vivo efficacy and therapeutic index. This review examines current methods for site-specific drug conjugation to antibodies, and compares in vivo results with their non-specifically conjugated counterparts. The apparent improvement in pharmacokinetics and the reduced off target toxicity warrant further development of this site-specific modification approach for future ADC development.
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