Abstract
Advancement in sequencing technologies allows for the identification of molecular pathways involved in tumor progression and treatment resistance. Implementation of novel agents targeting these pathways, defined as targeted therapy, significantly improves the prognosis of cancer patients. Targeted therapy also includes the use of monoclonal antibodies (mAbs). These drugs recognize specific oncogenic proteins expressed in cancer cells. However, as with many other types of targeting agents, mAb-based therapy usually fails in the long-term control of cancer progression due to the development of resistance. In many cases, resistance is caused by the activation of alternative pathways involved in cancer progression and the development of immune evasion mechanisms. To overcome this off-target resistance, bispecific antibodies (bsAbs) were developed to simultaneously target differential oncogenic pathway components, tumor-associated antigens (TAA) and immune regulatory molecules. As a result, in the last few years, several bsAbs have been tested or are being tested in cancer patients. A few of them are currently approved for the treatment of some hematologic malignancies but no bsAbs are approved in solid tumors. In this review, we will provide an overview of the state-of-the-art of bsAbs for the treatment of solid malignancies outlining their classification, design, main technologies utilized for production, mechanisms of action, updated clinical evidence and potential limitations.
Funder
Ministero dell’ Istruzione e del Merito (Progetti di Rilevante Interesse Nazionale
Reference150 articles.
1. Monoclonal Antibodies for the Treatment of Cancer;Shuptrine;Semin. Cancer Biol.,2012
2. IgG Subclasses and Allotypes: From Structure to Effector Functions;Vidarsson;Front. Immunol.,2014
3. The Hydrolysis of Rabbit Y-Globulin and Antibodies with Crystalline Papain;Porter;Biochem. J.,1959
4. Chiu, M.L., Goulet, D.R., Teplyakov, A., and Gilliland, G.L. Antibody Structure and Function: The Basis for Engineering Therapeutics. Antibodies, 2019. 8.
5. Boosting ADCC and CDC Activity by Fc Engineering and Evaluation of Antibody Effector Functions;Kellner;Methods,2014
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