Technological advancements in antibody-based therapeutics for treatment of diseases
Monoclonal antibodies (mAbs) represent a major class of therapeutics with widespread clinical applications in oncology, immunology, hematology, neurology and infectious disease. Since the introduction of hybridoma technology in 1975, the field has been advanced by a succession of innovations including chimeric and humanized antibody engineering, phage display, transgenic mouse platforms and high-throughput single B cell isolation. These technological developments have enhanced the specificity, potency and safety of mAbs, resulting in 144 FDA-approved antibody drugs on the market and 1,516 worldwide candidates in clinical development as of August 2025. Engineering breakthroughs have led to new modalities of antibody-based therapeutics, such as antibody-drug conjugates (ADCs), bispecific antibodies (bsAbs), and chimeric antigen receptor T (CAR-T) cell therapies. Each of these modalities has therapeutic utility across multiple disease domains. Recent advances in delivery strategies, notably mRNA-lipid nanoparticles (LNPs) and antibody-directed in vivo CAR-T cell reprogramming, can enable precision therapies while reducing off-target effects and manufacturing complexity. The integration of artificial intelligence (AI) and machine learning (ML), next-generation sequencing (NGS), and structural modeling tools has further accelerated antibody discovery, affinity maturation and immunogenicity prediction, allowing for more efficient and rational antibody design. The advances in antibody technology are reflected in the rapid market growth of antibody-based therapeutics, which had global sales exceeding USD 267 billion in 2024. This review provides a comprehensive update on recent developments in antibody discovery platforms, therapeutic formats and market trends, highlighting emerging strategies that are reshaping the landscape of antibody-based medicine. Furthermore, we discuss clinical translation, regulatory landscapes, and the integration of engineering, biology and informatics. Together, these aspects shape a dynamic and multidisciplinary future for the therapeutic antibody field, which is poised to address unmet clinical needs and global healthcare priorities.
Authors
- Nai-Lin Chou
- Yi‐Jen Su (ORCID: https://orcid.org/0000-0001-7622-7269)
- Kang-Hao Liang (ORCID: https://orcid.org/0000-0003-3942-0259)
- Hung‐Pin Peng (ORCID: https://orcid.org/0000-0002-9398-8120)
- Chi-Yung Chen
- Shih-Han Ko (ORCID: https://orcid.org/0000-0002-7284-4451)
- Hsiao-Ling Chiang (ORCID: https://orcid.org/0000-0002-8070-3771)
- Ruei‐Min Lu (ORCID: https://orcid.org/0000-0003-3792-5499)
- Joyce Pei‐Yi Yuan (ORCID: https://orcid.org/0000-0002-7028-186X)
- Hsiu-Hua Wang
- Han‐Chung Wu (ORCID: https://orcid.org/0000-0002-5185-1169)
- Sushree Shankar Panda
- Hung-Ju Hsu
- Monika Kumari (ORCID: https://orcid.org/0009-0003-7691-495X)
- Yi-Ting Tse
Institutions
- Institute of Biomedical Sciences, Academia Sinica (TW)
- Institute of Cellular and Organismic Biology, Academia Sinica (TW)
- Taipei Medical University (TW)
- Academia Sinica (TW)
Publication Details
- Journal
- Journal of Biomedical Science
- Published
- 2025-11-12
- DOI
- https://doi.org/10.1186/s12929-025-01190-2
- Citations
- 8
- Primary Topic
- Monoclonal and Polyclonal Antibodies Research
- Type
- article
- Field-Weighted Citation Impact
- 10.88