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<p>Chronic rejection (CR) remains the leading cause of morbidity and mortality in heart transplantation survivors. The primary pathological features of CR encompass cardiac allograft vasculopathy and myocardial fibrosis. Currently, its diagnosis heavily relies on invasive procedures, underscoring the pressing need for non-invasive evaluation methods. This study introduces a novel approach utilizing mannose-modified microbubbles (MB<sub>man</sub>) targeting CD206 (mannose receptor) positive M2 macrophages for early CR detection. In vitro experiments demonstrate substantial adhesion of MB<sub>man</sub> to M2 macrophages compared to common microbubbles (MB<sub>con</sub>). In a CR rat model, MB<sub>man</sub> and MB<sub>con</sub> are administered at three distinct time points (2 weeks, 4 weeks, and 6 weeks), followed by contrast-enhanced ultrasound images and quantitative analysis using the ultrasound destruction-supplementation method. Starting at 2 weeks and continuing through 6 weeks, MB<sub>man</sub> demonstrates significantly higher signal intensity than MB<sub>con</sub> in allograft rats. However, this difference is not observed in isograft rats at any of the indicated time points. These findings suggest an increase in M2 macrophage infiltration in allografts compared to isografts. Furthermore, the signal intensity of MB<sub>man</sub> positively correlates with the percentage of CD206 in allograft rats. This study proposes a promising approach, simultaneous noninvasive ultrasound molecular imaging, for the early-stage evaluation of CR.</p>

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Ultrasound molecular imaging of M2 macrophages for early detection of chronic rejection in heart transplantation

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年8月22日

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  • Jia Xu,
  • Cheng Deng,
  • Tang Gao,
  • Mengrong He,
  • Wenpei Fu,
  • Xin Zhang,
  • Yin Bai,
  • Jiani Qiu,
  • Rui Wang,
  • Yihan Chen,
  • Qiaofeng Jin,
  • Li Zhang,
  • Qing Lv,
  • Mingxing Xie,
  • Wenqian Wu

摘要

Chronic rejection (CR) remains the leading cause of morbidity and mortality in heart transplantation survivors. The primary pathological features of CR encompass cardiac allograft vasculopathy and myocardial fibrosis. Currently, its diagnosis heavily relies on invasive procedures, underscoring the pressing need for non-invasive evaluation methods. This study introduces a novel approach utilizing mannose-modified microbubbles (MBman) targeting CD206 (mannose receptor) positive M2 macrophages for early CR detection. In vitro experiments demonstrate substantial adhesion of MBman to M2 macrophages compared to common microbubbles (MBcon). In a CR rat model, MBman and MBcon are administered at three distinct time points (2 weeks, 4 weeks, and 6 weeks), followed by contrast-enhanced ultrasound images and quantitative analysis using the ultrasound destruction-supplementation method. Starting at 2 weeks and continuing through 6 weeks, MBman demonstrates significantly higher signal intensity than MBcon in allograft rats. However, this difference is not observed in isograft rats at any of the indicated time points. These findings suggest an increase in M2 macrophage infiltration in allografts compared to isografts. Furthermore, the signal intensity of MBman positively correlates with the percentage of CD206 in allograft rats. This study proposes a promising approach, simultaneous noninvasive ultrasound molecular imaging, for the early-stage evaluation of CR.