Scholarlink

Background <p>Zampilimab is a humanized monoclonal antibody that selectively inhibits transamidation of human tissue transglutaminase-2 (hTG2), an enzymatic activity implicated in the development of Idiopathic Pulmonary Fibrosis (IPF). Since measuring target occupancy (TO) non-invasively in the lung is challenging, in this study, we evaluated the feasibility to radiolabel zampilimab and longitudinally measure its TO in the murine lung with nuclear imaging using single photon computed tomography (SPECT).</p> Methods <p>Zampilimab was bioconjugated with DOTAGA and radiolabeled with Indium-111, then administered intravenously to nude female mice receiving hTG2-positive cells either subcutaneously (s.c.) or intratracheally (i.t.). In blocking groups, [<sup>111</sup>In]In-DOTAGA-zampilimab was simultaneously injected with a 100X excess of unlabeled antibody. SPECT imaging was performed for three days following [<sup>111</sup>In]In-DOTAGA-zampilimab administration.</p> Results <p>For all the timepoints, SPECT imaging revealed a significant uptake of radiolabeled zampilimab in hTG2-positive s.c. tumors. Furthermore, mice receiving exogenous cells i.t. displayed a greater pulmonary uptake of [<sup>111</sup>In]In-DOTAGA-zampilimab compared to the control group. The binding specificity of zampilimab to hTG2 was confirmed with competition experiments in which the administration of excess unlabeled zampilimab significantly prevented the uptake of the radiolabeled antibody.</p> Conclusions <p>The administration of hTG2-positive cells provided a straightforward and cost-effective animal model for evaluating the TO of zampilimab. Results derived from the i.t. administration model consistently confirmed that zampilimab can reach the lung and specifically bind hTG2. Additionally, our study demonstrated that zampilimab can be effectively radiolabeled for SPECT imaging, allowing for a non-invasive and quantitative assessment of lung TO, paving the way to its clinical application.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

SPECT as a translational non-invasive method to assess occupancy of the tissue transglutaminase-2 by zampilimab in the mouse lung

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年2月12日

查看全文
  • Pierre-Simon Bellaye,
  • Erica Ferrini,
  • Michaël Claron,
  • Alexandre Dias,
  • Costanza Bonfini,
  • Gino Villetti,
  • Anna Maria Capelli,
  • Timothy Johnson,
  • Bertrand Collin,
  • Franco Fabio Stellari

摘要

Background

Zampilimab is a humanized monoclonal antibody that selectively inhibits transamidation of human tissue transglutaminase-2 (hTG2), an enzymatic activity implicated in the development of Idiopathic Pulmonary Fibrosis (IPF). Since measuring target occupancy (TO) non-invasively in the lung is challenging, in this study, we evaluated the feasibility to radiolabel zampilimab and longitudinally measure its TO in the murine lung with nuclear imaging using single photon computed tomography (SPECT).

Methods

Zampilimab was bioconjugated with DOTAGA and radiolabeled with Indium-111, then administered intravenously to nude female mice receiving hTG2-positive cells either subcutaneously (s.c.) or intratracheally (i.t.). In blocking groups, [111In]In-DOTAGA-zampilimab was simultaneously injected with a 100X excess of unlabeled antibody. SPECT imaging was performed for three days following [111In]In-DOTAGA-zampilimab administration.

Results

For all the timepoints, SPECT imaging revealed a significant uptake of radiolabeled zampilimab in hTG2-positive s.c. tumors. Furthermore, mice receiving exogenous cells i.t. displayed a greater pulmonary uptake of [111In]In-DOTAGA-zampilimab compared to the control group. The binding specificity of zampilimab to hTG2 was confirmed with competition experiments in which the administration of excess unlabeled zampilimab significantly prevented the uptake of the radiolabeled antibody.

Conclusions

The administration of hTG2-positive cells provided a straightforward and cost-effective animal model for evaluating the TO of zampilimab. Results derived from the i.t. administration model consistently confirmed that zampilimab can reach the lung and specifically bind hTG2. Additionally, our study demonstrated that zampilimab can be effectively radiolabeled for SPECT imaging, allowing for a non-invasive and quantitative assessment of lung TO, paving the way to its clinical application.