| Literature DB >> 34255474 |
Joshua T Mattila1,2, Wissam Beaino3, Alexander G White4, Lea Nyiranshuti5, Pauline Maiello4, Jaime Tomko4, L James Frye4, Daniel Fillmore4, Charles A Scanga2,4, Philana Ling Lin2,6, JoAnne L Flynn2,5, Carolyn J Anderson3,5,7,8,9.
Abstract
Neutrophilic inflammation correlates with severe tuberculosis (TB), a disease caused by Mycobacterium tuberculosis (Mtb). Granulomas are lesions that form in TB, and a PET probe for following neutrophil recruitment to granulomas could predict disease progression. We tested the formyl peptide receptor 1 (FPR1)-targeting peptide FLFLF in Mtb-infected macaques. Preliminary studies in mice demonstrated specificity for neutrophils. In macaques, 64Cu-FLFLF was retained in lung granulomas and analysis of lung granulomas identified positive correlations between 64Cu-FLFLF and neutrophil and macrophage numbers (R2 = 0.8681 and 0.7643, respectively), and weaker correlations for T cells and B cells (R2 = 0.5744 and 0.5908, respectively), suggesting that multiple cell types drive 64Cu-FLFLF avidity. By PET/CT imaging, we found that granulomas retained 64Cu-FLFLF but with less avidity than the glucose analog 18F-FDG. These studies suggest that neutrophil-specific probes have potential PET/CT applications in TB, but important issues need to be addressed before they can be used in nonhuman primates and humans.Entities:
Keywords: PET/CT; formyl peptide receptor; granuloma; neutrophil; tuberculosis
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Year: 2021 PMID: 34255474 PMCID: PMC8744071 DOI: 10.1021/acsinfecdis.0c00826
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.578