| Literature DB >> 28614804 |
Nataliya P Buxbaum1, Donald E Farthing1, Natella Maglakelidze1, Martin Lizak2, Hellmut Merkle3, Andrea C Carpenter4, Brittany U Oliver1, Veena Kapoor1, Ehydel Castro1, Gregory A Swan1, Liliane M Dos Santos5, Nicolas J Bouladoux5, Catherine V Bare1, Francis A Flomerfelt1, Michael A Eckhaus6, William G Telford1, Yasmine Belkaid5, Remy J Bosselut4, Ronald E Gress1.
Abstract
Hematopoietic stem cell transplantation (HSCT) offers a cure for cancers that are refractory to chemotherapy and radiation. Most HSCT recipients develop chronic graft-versus-host disease (cGVHD), a systemic alloimmune attack on host organs. Diagnosis is based on clinical signs and symptoms, as biopsies are risky. T cells are central to the biology of cGVHD. We found that a low Treg/CD4+ T effector memory (Tem) ratio in circulation, lymphoid, and target organs identified early and established mouse cGVHD. Using deuterated water labeling to measure multicompartment in vivo kinetics of these subsets, we show robust Tem and Treg proliferation in lymphoid and target organs, while Tregs undergo apoptosis in target organs. Since deuterium enrichment into DNA serves as a proxy for cell proliferation, we developed a whole-body clinically relevant deuterium MRI approach to nonradioactively detect cGVHD and potentially allow imaging of other diseases characterized by rapidly proliferating cells.Entities:
Keywords: Immunology; Transplantation
Year: 2017 PMID: 28614804 PMCID: PMC5470940 DOI: 10.1172/jci.insight.92851
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708