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

成果类型:
Article
署名作者:
Farid, Ali Salehi; Rowley, Jennifer E.; Allen, Harris H.; Kruger, Isabella G.; Tavakolpour, Soheil; Neeley, Kyle; Cong, Min; Shahbazian, Haneyeh; Dorafshani, Niki; Berrada, Achraf; Macdonagh, Alexander C.; Padera, Robert F.; Brugarolas, Pedro; Packard, Alan B.; Rosenbaum, Matthew W.; Divakaran, Sanjay; Di Carli, Marcelo F.; Rashidian, Mohammad
署名单位:
Harvard University; Harvard University Medical Affiliates; Dana-Farber Cancer Institute; Harvard University; Harvard Medical School; Harvard University; Harvard University Medical Affiliates; Massachusetts General Hospital; Harvard University; Harvard University Medical Affiliates; Brigham & Women's Hospital; Harvard University; Harvard University Medical Affiliates; Boston Children's Hospital; Harvard University; Harvard University Medical Affiliates; Beth Israel Deaconess Medical Center; Harvard Medical School; Harvard University; Harvard University Medical Affiliates; Brigham & Women's Hospital; Harvard Medical School; Harvard University; Harvard University Medical Affiliates; Brigham & Women's Hospital; Harvard Medical School; Harvard University; Harvard University Medical Affiliates; Brigham & Women's Hospital; Harvard Medical School
刊物名称:
Nature
ISSN/ISSBN:
0028-2197
DOI:
10.1038/s41586-024-08441-6
发表日期:
2025-03-06
关键词:
disease f-18-fdg cancer antibodies biopsy injury
摘要:
Imaging inflammation holds immense potential for advancing the diagnosis, treatment and prognosis of many conditions1, 2-3. 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.