Macrophage regulation of graft-vs-host disease

YQ Hong, B Wan, XF Li - World Journal of Clinical Cases, 2020 - pmc.ncbi.nlm.nih.gov
YQ Hong, B Wan, XF Li
World Journal of Clinical Cases, 2020pmc.ncbi.nlm.nih.gov
Hematopoietic stem cell transplantation has become a curative choice of many
hematopoietic malignancy, but graft-vs-host disease (GVHD) has limited the survival quality
and overall survival of hematopoietic stem cell transplantation. Understanding of the
immune cells' reaction in pathophysiology of GVHD has improved, but a review on the role
of macrophages in GVHD is still absent. Studies have observed that macrophage infiltration
is associated with GVHD occurrence and development. In this review, we summarize and …
Hematopoietic stem cell transplantation has become a curative choice of many hematopoietic malignancy, but graft-vs-host disease (GVHD) has limited the survival quality and overall survival of hematopoietic stem cell transplantation. Understanding of the immune cells’ reaction in pathophysiology of GVHD has improved, but a review on the role of macrophages in GVHD is still absent. Studies have observed that macrophage infiltration is associated with GVHD occurrence and development. In this review, we summarize and analyze the role of macrophages in GVHD based on pathophysiology of acute and chronic GVHD, focusing on the macrophage recruitment and infiltration, macrophage polarization, macrophage secretion, and especially interaction of macrophages with other immune cells. We could conclude that macrophage recruitment and infiltration contribute to both acute and chronic GVHD. Based on distinguishing pathology of acute and chronic GVHD, macrophages tend to show a higher M1/M2 ratio in acute GVHD and a lower M1/M2 ratio in chronic GVHD. However, the influence of dominant cytokines in GVHD is controversial and inconsistent with macrophage polarization. In addition, interaction of macrophages with alloreactive T cells plays an important role in acute GVHD. Meanwhile, the interaction among macrophages, B cells, fibroblasts, and CD4+ T cells participates in chronic GVHD development.
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