Visualization of activated T cells by OX40-ImmunoPET as a strategy for diagnosis of acute graft-versus-host disease
Cancer Research, ISSN: 1538-7445, Vol: 80, Issue: 21, Page: 4780-4790
2020
- 25Citations
- 15Captures
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Metrics Details
- Citations25
- Citation Indexes25
- 25
- CrossRef8
- Captures15
- Readers15
- 15
Article Description
Graft-versus-host disease (GvHD) is a major complication of allogeneic hematopoietic cell transplantation (HCT), mediated primarily by donor T cells that become activated and attack host tissues. Noninvasive strategies detecting T-cell activation would allow for early diagnosis and possibly more effective management of HCT recipients. PET imaging is a sensitive and clinically relevant modality ideal for GvHD diagnosis, and there is a strong rationale for the use of PET tracers that can monitor T-cell activation and expansion with high specificity. The TNF receptor superfamily member OX40 (CD134) is a cell surface marker that is highly specific for activated T cells, is upregulated during GvHD, and mediates disease pathogenesis. We recently reported the development of an antibody-based activated T-cell imaging agent targeting OX40. In the present study, we visualize the dynamics of OX40 expression in an MHC-mismatch mouse model of acute GvHD using OX40-immunoPET. This approach enabled visualization of T-cell activation at early stages of disease, prior to overt clinical symptoms with high sensitivity and specificity. This study highlights the potential utility of the OX40 PET imaging as a new strategy for GvHD diagnosis and therapy monitoring.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85097498850&origin=inward; http://dx.doi.org/10.1158/0008-5472.can-20-1149; http://www.ncbi.nlm.nih.gov/pubmed/32900772; https://aacrjournals.org/cancerres/article/80/21/4780/646058/Visualization-of-Activated-T-Cells-by-OX40; https://dx.doi.org/10.1158/0008-5472.can-20-1149; https://cancerres.aacrjournals.org/content/80/21/4780
American Association for Cancer Research (AACR)
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