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Updated: Jul 7, 2025

Analyzing Tumor and Tissue Distribution of Target Antigen Specific Therapeutic Antibody
Published on: May 16, 2020
Therapeutic Monoclonal Antibodies against Cancer: Present and Future
Marisa Delgado1, Jose A Garcia-Sanz1
1Department of Molecular Biomedicine, Centro de Investigaciones Biológicas Margarita Salas (CIB-CSIC), 28040 Madrid, Spain.
Abstract:
A series of monoclonal antibodies with therapeutic potential against cancer have been generated and developed. Ninety-one are currently used in the clinics, either alone or in combination with chemotherapeutic agents or other antibodies, including immune checkpoint antibodies. These advances helped to coin the term personalized medicine or precision medicine. However, it seems evident that in addition to the current work on the analysis of mechanisms to overcome drug resistance, the use of different classes of antibodies (IgA, IgE, or IgM) instead of IgG, the engineering of the Ig molecules to increase their half-life, the acquisition of additional effector functions, or the advantages associated with the use of agonistic antibodies, to allow a broad prospective usage of precision medicine successfully, a strategy change is required. Here, we discuss our view on how these strategic changes should be implemented and consider their pros and cons using therapeutic antibodies against cancer as a model. The same strategy can be applied to therapeutic antibodies against other diseases, such as infectious or autoimmune diseases.
Insights
Monoclonal antibodies are revolutionizing cancer treatment, enabling precision medicine. A strategic shift is needed to broaden their use by exploring new antibody types and engineering for enhanced efficacy against various diseases.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Monoclonal antibodies (mAbs) are pivotal in modern cancer therapy, with 91 currently in clinical use, often combined with chemotherapy or other immunotherapies like immune checkpoint inhibitors.
- These advancements have driven the paradigm of personalized or precision medicine in oncology.
- Despite successes, challenges like drug resistance necessitate further innovation.
Purpose of the Study:
- To propose a strategic shift in therapeutic antibody development beyond current IgG-based approaches.
- To explore the potential of alternative antibody classes (IgA, IgE, IgM) and engineered antibody variants for broader therapeutic applications.
- To discuss the advantages and disadvantages of these strategic changes using cancer therapeutics as a model.
Main Methods:
- Review and strategic analysis of therapeutic antibody development.
- Discussion of engineering strategies to enhance antibody half-life and effector functions.
- Consideration of agonistic antibodies and alternative antibody isotypes (IgA, IgE, IgM).
Main Results:
- Current therapeutic antibodies, primarily IgG, are effective but face limitations.
- Exploring diverse antibody classes and engineering novel antibody formats can overcome resistance and enhance efficacy.
- Strategic implementation of these changes is crucial for expanding precision medicine.
Conclusions:
- A paradigm shift in antibody development is required to fully realize the potential of precision medicine.
- Incorporating diverse antibody classes and advanced engineering offers a promising future for antibody therapeutics.
- The proposed strategies are applicable to antibody therapies for infectious and autoimmune diseases as well as cancer.
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