<p>Imaging inflammation holds immense potential for advancing the diagnosis, treatment and prognosis of many conditions<sup><CitationRef AdditionalCitationIDS="CR2" CitationID="CR1">1</CitationRef>–<CitationRef CitationID="CR3">3</CitationRef></sup>. The lack of a specific and sensitive positron emission tomography (PET) probe to detect inflammation is a critical challenge. To bridge this gap, we present CD45-PET imaging, which detects inflammation with exceptional sensitivity and clarity in several preclinical models. Notably, the intensity of the&#xa0;CD45-PET signal&#xa0;correlates&#xa0;robustly&#xa0;with the severity of disease&#xa0;in models of inflammatory lung and bowel diseases, outperforming <sup>18</sup>F-fluorodeoxyglucose PET, the most widely used imaging modality for inflammation globally. Longitudinal CD45-PET imaging further enables precise monitoring of dynamic changes in tissue-specific inflammatory profiles. Finally, we developed a human CD45-PET probe for clinical translation that effectively detects human immune cells in a humanized mouse model. CD45-PET imaging holds substantial clinical promise, offering a tool for guiding&#xa0;diagnostic and therapeutic&#xa0;decisions&#xa0;for inflammatory diseases through a precise, whole-body&#xa0;assessment of the inflammation&#xa0;profiles&#xa0;of&#xa0;individual patients.</p>

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CD45-PET is a robust, non-invasive tool for imaging inflammation

  • Ali Salehi Farid,
  • Jennifer E. Rowley,
  • Harris H. Allen,
  • Isabella G. Kruger,
  • Soheil Tavakolpour,
  • Kyle Neeley,
  • Min Cong,
  • Haneyeh Shahbazian,
  • Niki Dorafshani,
  • Achraf Berrada,
  • Alexander C. MacDonagh,
  • Robert F. Padera,
  • Pedro Brugarolas,
  • Alan B. Packard,
  • Matthew W. Rosenbaum,
  • Sanjay Divakaran,
  • Marcelo F. Di Carli,
  • Mohammad Rashidian

摘要

Imaging inflammation holds immense potential for advancing the diagnosis, treatment and prognosis of many conditions13. The lack of a specific and sensitive positron emission tomography (PET) probe to detect inflammation is a critical challenge. To bridge this gap, we present CD45-PET imaging, which detects inflammation with exceptional sensitivity and clarity in several preclinical models. Notably, the intensity of the CD45-PET signal correlates robustly with the severity of disease in models of inflammatory lung and bowel diseases, outperforming 18F-fluorodeoxyglucose PET, the most widely used imaging modality for inflammation globally. Longitudinal CD45-PET imaging further enables precise monitoring of dynamic changes in tissue-specific inflammatory profiles. Finally, we developed a human CD45-PET probe for clinical translation that effectively detects human immune cells in a humanized mouse model. CD45-PET imaging holds substantial clinical promise, offering a tool for guiding diagnostic and therapeutic decisions for inflammatory diseases through a precise, whole-body assessment of the inflammation profiles of individual patients.