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Effect and mechanism of HER2 antibody-drug conjugate combined with anti-PD-1 antibody in mouse bladder cancer models
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Shuo HE1, Lu TAO1, Yue WU1, Mengting SHI1, Tiantian ZHANG1, Yuanyuan GUO2, Rui WANG1, 3
Journal of Army Medical University | 2025, 47(14) : 1623 - 1631
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Journal of Army Medical University | 2025, 47(14): 1623-1631
• Basic Medicine •
Effect and mechanism of HER2 antibody-drug conjugate combined with anti-PD-1 antibody in mouse bladder cancer models
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Shuo HE1, Lu TAO1, Yue WU1, Mengting SHI1, Tiantian ZHANG1, Yuanyuan GUO2, Rui WANG1, 3
Affiliations
  • 1Department of Medical Oncology, First Affiliated Hospital of Bengbu Medical University,Bengbu,Anhui,China
  • 2Department of Urology, First Affiliated Hospital of Bengbu Medical University,Bengbu,Anhui,China
  • 3Anhui Provincial Key Laboratory of Tumor Evolution and Intelligent Diagnosis and Treatment, First Affiliated Hospital of Bengbu Medical University,Bengbu,Anhui,China
Published: 2025-07-30 doi: 10.16016/j.2097-0927.202504097
Outline
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Objective‍

To investigate the synergistic therapeutic effects of HER2 antibody-drug conjugate (HER2-ADC) combined with anti-PD-1 antibody (anti-PD-1) on HER2-expressing bladder cancer and elucidate its regulatory mechanisms on the tumor immune microenvironment.

Methods‍

Orthotopic tumor models were established in 40 female C57BL/6 mice (6~8 weeks old, body mass 18~22 g) using MB49 bladder cancer cells overexpressing human HER2. When tumors reached 100 mm³, the mice were randomized into (n=10) control (intraperitoneal injection of 1.0 mL PBS), anti-PD-1 (200 µg per mouse every 3 d), HER2-ADC (2.5 mg/kg once weekly), and combination groups (same regimens as above monotherapy). Tumor volume and body mass were measured every 3 d during 28-day treatment. Tumor growth kinetics and survival rates were analyzed. Post-treatment survival was monitored until natural death to determine median survival time (n=5). At day 28, blood and tumor samples (n=5) were collected to detect myeloid-derived suppressor cells (MDSCs; CD11b⁺Gr1⁺) and regulatory T cells (Tregs; CD4⁺CD25⁺FOXP3⁺) with flow cytometry, tumor-infiltrating CD3⁺T, CD8⁺T, and FOXP3⁺T cells with immunohistochemical assasy, and liver/kidney functions [alanine aminotransferase (ALT), aspartate aminotransferase (AST), blood urea nitrogen (BUN), creatinine (CRE)] and tissue damage indicators [lactate dehydrogenase isoenzyme (LDH-L)].

Results‍

In 28 d after treatment, the combination group obtained significantly smallest tumor volume than the control group and the 2 monotherapy groups (all P<0.01). The longest median survival was observed in the combination group (65 d, P<0.01), followed by the HER2-ADC group (55 d), anti-PD-1 group (53 d) and control group (41 d). After 28 d of treatment, the combination group exhibited obviously the smallest peripheral proportions of MDSCs/Tregs, most tumor-infiltrating CD3⁺T/CD8⁺T cells, and less FOXP3⁺T cells when compared with the 2 monotherapy groups and control group (all P<0.05). While, the 2 monotherapy groups had smaller MDSCs/Tregs proportions than the control group (P<0.05). No significant differences were observed among the 4 groups in serum ALT, AST, BUN, CRE, or LDH-L levels, and all of them were within normal ranges.

Conclusion‍

HER2-ADC combined with anti-PD-1 suppresses the growth of orthotopic bladder tumor, probably through their synergic effects on down-regulating MDSCs/Treg and enhancing CD8⁺T cell infiltration.

urinary bladder neoplasms  /  HER2 antibody-drug conjugate  /  anti-PD-1 antibody  /  tumor microenvironment
何硕, 陶璐, 武越, 史梦婷, 张甜甜, 郭园园, 汪蕊. 抗HER2抗体偶联药物联合抗PD-1单抗对小鼠膀胱肿瘤的作用及机制研究. 陆军军医大学学报, 2025 , 47 (14) : 1623 -1631 . DOI: 10.16016/j.2097-0927.202504097
Shuo HE, Lu TAO, Yue WU, Mengting SHI, Tiantian ZHANG, Yuanyuan GUO, Rui WANG. Effect and mechanism of HER2 antibody-drug conjugate combined with anti-PD-1 antibody in mouse bladder cancer models[J]. Journal of Army Medical University, 2025 , 47 (14) : 1623 -1631 . DOI: 10.16016/j.2097-0927.202504097
Year 2025 volume 47 Issue 14
29
11
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Article Info
doi: 10.16016/j.2097-0927.202504097
  • Receive Date:2025-04-26
  • Online Date:2026-10-28
  • Published:2025-07-30
Article Data
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History
  • Received:2025-04-26
  • Revised:2025-06-18
Affiliations
    1Department of Medical Oncology, First Affiliated Hospital of Bengbu Medical University,Bengbu,Anhui,China
    2Department of Urology, First Affiliated Hospital of Bengbu Medical University,Bengbu,Anhui,China
    3Anhui Provincial Key Laboratory of Tumor Evolution and Intelligent Diagnosis and Treatment, First Affiliated Hospital of Bengbu Medical University,Bengbu,Anhui,China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
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属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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