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CD11b-Based Pre-Targeted SPECT/CT Imaging Allows for the Detection of Inflammation in Aortic Aneurysm.
Zhou, Xiaonan; Zhu, Kai; Zhang, Yiqiu; Ming, Yang; Shi, Dai; Tan, Hui; Xiang, Bitao; Zhu, Shichao; Cheng, Dengfeng; Lai, Hao; Wang, Chunsheng; Liu, Guobing.
Afiliação
  • Zhou X; Department of Cardiac Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, People's Republic of China.
  • Zhu K; Shanghai Institute of Cardiovascular Diseases, Shanghai, 200032, People's Republic of China.
  • Zhang Y; Department of Cardiac Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, People's Republic of China.
  • Ming Y; Shanghai Institute of Cardiovascular Diseases, Shanghai, 200032, People's Republic of China.
  • Shi D; Department of Nuclear Medicine, Zhongshan Hospital, Fudan University, Shanghai, 200032, People's Republic of China.
  • Tan H; Institute of Nuclear Medicine, Fudan University, Shanghai, 200032, People's Republic of China.
  • Xiang B; Shanghai Institute of Medical Imaging, Shanghai, 200032, People's Republic of China.
  • Zhu S; Department of Cardiac Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, People's Republic of China.
  • Cheng D; Shanghai Institute of Cardiovascular Diseases, Shanghai, 200032, People's Republic of China.
  • Lai H; Department of Nuclear Medicine, Zhongshan Hospital, Fudan University, Shanghai, 200032, People's Republic of China.
  • Wang C; Institute of Nuclear Medicine, Fudan University, Shanghai, 200032, People's Republic of China.
  • Liu G; Shanghai Institute of Medical Imaging, Shanghai, 200032, People's Republic of China.
J Inflamm Res ; 15: 1921-1933, 2022.
Article em En | MEDLINE | ID: mdl-35321320
ABSTRACT

Purpose:

To investigate the feasibility of a pre-targeted imaging strategy based on the cycloaddition between 1,2,4,5-terazine (Tz) and trans-cyclooctene (TCO) for evaluating CD11b expression in inflammatory aortic aneurysm (AA) using single photon emission computed tomography/computed tomography (SPECT/CT).

Methods:

C57BL/6J mice were fed ß-aminopropionitrile (1 g/kg/day) for 4 weeks to establish AA models. Anti-CD11b-TCO was synthesized and 99mTc-HYNIC-PEG11-Tz was designed for pre-targeted SPECT/CT. The affinity and specificity of the probe for the inflammatory cell line Raw-264.7 were investigated. Then, anti-CD11b-TCO pre-targeted and 99mTc-HYNIC-PEG11-Tz based SPECT/CT were performed to detect in vivo inflammation in AA. Finally, ex vivo aortic breast-specific gamma imaging (BSGI), Western blot assays, and immunohistochemical CD11b staining were performed to confirm the in vivo findings of SPECT/CT.

Results:

In the AA models, 65.22% (15/23) had aortic lesions, including 43.48% (10/23) AA lesions. The anti-CD11b-TCO presented with a high TCO coupling ratio (7.43), and the 99mTc-HYNIC-PEG11-Tz showed high radio-purity (>95%), good in vitro stability and a rapid clearance rate. Additionally, anti-CD11b-TCO and 99mTc-HYNIC-PEG11-Tz presented high click rate (~89%). The in vitro clicked compound, 99mTc-HYNIC-PEG11-Tz/TCO-anti-CD11b, showed high affinity and specificity for Raw-264.7 cells. 99mTc-HYNIC-PEG11-Tz/TCO-anti-CD11b pre-targeting SPECT/CT successfully demonstrated inflammatory AA with a high AA-to-background ratio in AA mice, compared to AA mice that were injected with 99mTc-HYNIC-Tz/TCO-IgG (8.13 versus 3.71, P < 0.001) and control mice injected with 99mTc-HYNIC-Tz/TCO-anti-CD11b (8.13 versus 3.66, P < 0.001). This result was confirmed by ex vivo BSGI performed immediately after SPECT/CT and immunohistochemical CD11b staining.

Conclusion:

SPECT/CT imaging using the anti-CD11b-TCO/Tz-PEG11-HYNIC-99mTc based pre-targeting imaging strategy allows for the detection of inflammation in progressive AA.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: J Inflamm Res Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: J Inflamm Res Ano de publicação: 2022 Tipo de documento: Article
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