HER2 Antibody–Nanogel Conjugates: A High-Capacity, Antibody-Sparing Alternative to Antibody–Drug Conjugates

HER2-targeted antibody-nanogel conjugates (ANCs) were developed with covalently encapsulated DM1 and benchmarked against the clinically optimized antibody-drug conjugate Kadcyla (T-DM1). In vitro, ANCs showed cytotoxicity comparable to that of T-DM1. In vivo, despite being at the proof-of-concept stage, HER2-DM1-ANC achieved equivalent antitumor efficacy in a BT-474 breast cancer xenograft model while requiring 4-fold less antibody. This reduced antibody usage may lessen the risk of tumor resistance, highlighting the unique advantage of the nanogel platform. The benefit stems from ANCs' higher drug-to-antibody ratio, achieved without chemical modification of the payload─a key bottleneck in ADC development. While T-DM1 represents a mature clinical product, these findings underscore ANCs as a high-capacity, modular nanoscale platform with significant potential for refinement and optimization in antibody-directed therapeutics.

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Publication Details

Journal
Nano Letters
Published
2025-12-23
DOI
https://doi.org/10.1021/acs.nanolett.5c04911
Primary Topic
HER2/EGFR in Cancer Research
Type
article
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article

HER2 Antibody–Nanogel Conjugates: A High-Capacity, Antibody-Sparing Alternative to Antibody–Drug Conjugates

Yasin Alp, Jingyi Qiu, S. Thayumanavan, Shuai Gong et al.
Nano Letters
HER2/EGFR in Cancer Research
article

HER2 Antibody–Nanogel Conjugates: A High-Capacity, Antibody-Sparing Alternative to Antibody–Drug Conjugates

Yasin Alp, Jingyi Qiu, S. Thayumanavan, Shuai Gong, D. Joseph Jerry, Paige Szipszky
article en

Abstract

HER2-targeted antibody-nanogel conjugates (ANCs) were developed with covalently encapsulated DM1 and benchmarked against the clinically optimized antibody-drug conjugate Kadcyla (T-DM1). In vitro, ANCs showed cytotoxicity comparable to that of T-DM1. In vivo, despite being at the proof-of-concept stage, HER2-DM1-ANC achieved equivalent antitumor efficacy in a BT-474 breast cancer xenograft model while requiring 4-fold less antibody. This reduced antibody usage may lessen the risk of tumor resistance, highlighting the unique advantage of the nanogel platform. The benefit stems from ANCs' higher drug-to-antibody ratio, achieved without chemical modification of the payload─a key bottleneck in ADC development. While T-DM1 represents a mature clinical product, these findings underscore ANCs as a high-capacity, modular nanoscale platform with significant potential for refinement and optimization in antibody-directed therapeutics.

Nano LettersVol. 26(1)
Good health and well-being
Openalex Percentile: Top 31%
HER2/EGFR in Cancer Research
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