| Literature DB >> 31296496 |
Sarah Morin-Zorman1, Christian Wysocki2, Jieqing Zhu3, Hongmei Li4, Sylvain Zorman5, Catherine Matte-Martone6,7, Edwina Kisanga6, Jennifer McNiff8, Dhanpat Jain9, David Gonzalez10, David M Rothstein3,11,12, Fadi G Lakkis3,11,12, Ann Haberman10, Warren D Shlomchik3,12,13.
Abstract
Graft-versus-host disease (GVHD) is a major cause of morbidity and mortality in allogeneic hematopoietic stem cell transplantation (alloSCT). By static microscopy, cutaneous GVHD lesions contain a mix of T cells and myeloid cells. We used 2-photon intravital microscopy to investigate the dynamics of CD4+ and CD8+ T cells and donor dendritic cells (DCs) in cutaneous GVHD lesions in an MHC-matched, multiple minor histocompatibility antigen-mismatched (miHA) model. The majority of CD4 and CD8 cells were stationary, and few cells entered and stopped or were stopped and left the imaged volumes. CD8 cells made TCR:MHCI-dependent interactions with CD11c+ cells, as measured by the durations that CD8 cells contacted MHCI+ vs MHCI- DCs. The acute deletion of Langerin+CD103+ DCs, which were relatively rare, did not affect CD8 cell motility and DC contact times, indicating that Langerin-CD103- DCs provide stop signals to CD8 cells. CD4 cells, in contrast, had similar contact durations with MHCII+ and MHCII- DCs. However, CD4 motility rapidly increased after the infusion of an MHCII-blocking antibody, indicating that TCR signaling actively suppressed CD4 movements. Many CD4 cells still were stationary after anti-MHCII antibody infusion, suggesting CD4 cell heterogeneity within the lesion. These data support a model of local GVHD maintenance within target tissues.Entities:
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Year: 2019 PMID: 31296496 PMCID: PMC6650737 DOI: 10.1182/bloodadvances.2019000227
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529