TY - JOUR
T1 - In vivo dynamics of T cells and their interactions with dendritic cells in mouse cutaneous graft-versus-host disease
AU - Morin-Zorman, Sarah
AU - Wysocki, Christian
AU - Zhu, Jieqing
AU - Li, Hongmei
AU - Zorman, Sylvain
AU - Matte-Martone, Catherine
AU - Kisanga, Edwina
AU - McNiff, Jennifer
AU - Jain, Dhanpat
AU - Gonzalez, David
AU - Rothstein, David M.
AU - Lakkis, Fadi G.
AU - Haberman, Ann
AU - Shlomchik, Warren D.
N1 - Funding Information:
The authors acknowledge the diligent care by the animal technicians at both Yale and the University of Pittsburgh. This work was supported by the National Institutes of Health, National Heart, Lung, and Blood Institute (R01-HL083072).
Funding Information:
This work was supported by the National Institutes of Health, National Heart, Lung, and Blood Institute (R01-HL083072).
Publisher Copyright:
© 2019 by The American Society of Hematology
PY - 2019/7/23
Y1 - 2019/7/23
N2 - 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 CD41 and CD81 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 CD11c1 cells, as measured by the durations that CD8 cells contacted MHCI1 vs MHCI2 DCs. The acute deletion of Langerin1CD1031 DCs, which were relatively rare, did not affect CD8 cell motility and DC contact times, indicating that Langerin2CD1032 DCs provide stop signals to CD8 cells. CD4 cells, in contrast, had similar contact durations with MHCII1 and MHCII2 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.
AB - 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 CD41 and CD81 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 CD11c1 cells, as measured by the durations that CD8 cells contacted MHCI1 vs MHCI2 DCs. The acute deletion of Langerin1CD1031 DCs, which were relatively rare, did not affect CD8 cell motility and DC contact times, indicating that Langerin2CD1032 DCs provide stop signals to CD8 cells. CD4 cells, in contrast, had similar contact durations with MHCII1 and MHCII2 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.
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U2 - 10.1182/bloodadvances.2019000227
DO - 10.1182/bloodadvances.2019000227
M3 - Article
C2 - 31296496
AN - SCOPUS:85069732052
SN - 2473-9529
VL - 3
SP - 2082
EP - 2092
JO - Blood Advances
JF - Blood Advances
IS - 14
ER -