Advances in Antibody–Drug Conjugates

A special issue of Pharmaceuticals (ISSN 1424-8247). This special issue belongs to the section "Pharmacology".

Deadline for manuscript submissions: 20 July 2026 | Viewed by 876

Special Issue Editor


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Guest Editor
Department of Cancer Systems Imaging, University of Texas MD Anderson Cancer Center, 1881 East Rd., Houston, TX 77054, USA
Interests: antibody-drug conjugates; radiotheranostics; bioconjugation; targeted radionuclide therapy; nanobody-drug conjugates; antibody-radionuclide conjugates; radiochemistry; biorthogonal click chemistry
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Special Issue Information

Dear Colleagues,

Antibody–drug conjugates (ADCs) have emerged as a powerful therapeutic modality by combining the high specificity of antibodies with the cytotoxic potency of chemotherapeutic agents. These engineered biopharmaceuticals have demonstrated remarkable success in targeted cancer therapy and are now being explored for broader applications, including autoimmune and infectious diseases. Advances in antibody engineering, linker stability, bioconjugation technology, payload potency and diversity, and tumor-specific targeting have paved the way for next-generation ADCs with improved efficacy and safety profiles. Despite their success, ADCs face challenges such as drug resistance, off-target toxicity, and manufacturing complexities. Addressing these issues requires interdisciplinary collaboration across biotechnology, pharmacology, and clinical sciences. This Special Issue aims to provide a comprehensive overview of cutting-edge research and novel technological developments in ADCs, offering insights into their future potential in precision medicine. We invite researchers, clinicians, and industry experts to contribute original research articles, reviews, and short communications covering, but not limited to, the following topics:

  • Novel antibody engineering approaches for improved targeting and efficacy;
  • Innovative linker technologies enhancing stability and controlled payload release;
  • Technological advancement in bioconjugation chemistry;
  • Emerging payloads and their mechanisms of action;
  • ADC pharmacokinetics, biodistribution, and resistance mechanisms;
  • Clinical advancements and regulatory considerations in ADC development;
  • Applications of ADCs beyond oncology, including autoimmune and infectious diseases;
  • Computational modeling and AI-driven design of next-generation ADCs;
  • Combination strategies integrating ADCs with immunotherapy and small molecules.

This Special Issue aims to provide a comprehensive overview of the current landscape and future potential of ADCs in precision medicine. We welcome high-quality contributions that will foster scientific discussion and innovation in this rapidly evolving field.

In addition, we would like to express special thanks to Ha Tran for her contributions to this Special Issue.

Dr. Aiko Yamaguchi
Guest Editor

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Keywords

  • antibody–drug conjugates
  • linker technology
  • bispecific antibodies
  • conditionally activated antibodies
  • degrader–antibody conjugates
  • antibody–immunotoxin conjugates
  • antibody–radionuclide conjugates
  • oncology
  • autoimmune disease
  • infectious disease

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Published Papers (1 paper)

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Research

10 pages, 841 KB  
Article
Radioimmunotherapy for Malignant Mesothelioma Targeting C-ERC/Mesothelin
by Hirofumi Hanaoka, Aiko Yamaguchi, Masahiro Maeda, Tatsuya Segawa and Noboru Oriuchi
Pharmaceuticals 2026, 19(3), 501; https://doi.org/10.3390/ph19030501 - 18 Mar 2026
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Abstract
Background/Objectives: Malignant mesothelioma has a poor prognosis and limited therapeutic options. C-ERC/mesothelin is highly expressed in mesotheliomas and is a potential target for radioimmunotherapy (RIT). This study evaluated the radiolabeled anti-C-ERC/mesothelin antibody mAb 22A31 as a therapeutic agent. Methods: C-ERC/mesothelin expression [...] Read more.
Background/Objectives: Malignant mesothelioma has a poor prognosis and limited therapeutic options. C-ERC/mesothelin is highly expressed in mesotheliomas and is a potential target for radioimmunotherapy (RIT). This study evaluated the radiolabeled anti-C-ERC/mesothelin antibody mAb 22A31 as a therapeutic agent. Methods: C-ERC/mesothelin expression in mesothelioma cell lines was assessed by Western blotting, and the specific binding of 125I-labeled mAb 22A31 was examined. Biodistribution of 111In-labeled mAb 22A31 was evaluated in a mesothelioma cell line, MSTO-211H tumor-bearing mice. The therapeutic efficacy of 90Y-labeled mAb 22A31 was evaluated in subcutaneous and pleural dissemination models. Results: mAb 22A31 showed specific binding considering the level of C-ERC/mesothelin expression in each mesothelioma cell line. 111In-mAb 22A31 accumulated in tumors with minimal uptake in normal tissues. 90Y-mAb 22A31 significantly delayed the growth of subcutaneous tumors and improved survival in a pleural dissemination model. Conclusions: Radiolabeled mAb 22A31 specifically targeted C-ERC/mesothelin and demonstrated therapeutic efficacy in a mesothelioma xerograph model. Therefore, 90Y-mAb 22A31 is a promising RIT agent and supports the further development of C-ERC/mesothelin-targeted therapy for mesothelioma. Full article
(This article belongs to the Special Issue Advances in Antibody–Drug Conjugates)
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