In vivo IL-4 prevents allo-antigen driven CD8 CTL development.

Clin Immunol

Division of Immunology, University of Cincinnati College of Medicine, Cincinnati, OH 45267, United States; Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, United States; Department of Medicine, Cincinnati Veterans Affairs Medical Center, Cincinnati, OH 45220, United States.

Published: July 2017

IL-4 has been shown to suppress acute graft vs. host disease (GVHD) in irradiated hosts. Here we evaluated whether IL-4 suppresses acute GVHD in the un-irradiated parent-into-F1 GVHD model with relevance to renal allograft rejection. IL-4 completely suppressed CD8 CTL when administered with donor cells however this effect was lost if its administration was delayed 3days. IL-4 did not inhibit donor CD8 T cell homing to the host spleen but rather prevented donor CD8 T cell differentiation into CTLs. Studies with IL-4Rα-deficient donor cells or recipient mice demonstrated that IL-4 effects on the host, rather than, or in addition to IL-4 effects on donor cells, were critical for suppression of CTL. Because IL-4 decreased all splenic dendritic cell populations and increased neutrophil and CD8 T cells, IL-4 may suppress donor CD8 CTL by decreasing Ag presentation and/or increasing host myeloid and CD8 T cell suppression of donor T cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484589PMC
http://dx.doi.org/10.1016/j.clim.2017.03.008DOI Listing

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