AI Article Synopsis

  • The study focused on comparing follicular helper T (Tfh) cell responses in renal grafts and spleens within a rat model of chronic allograft nephropathy (CAN).
  • Tissue samples from Fischer rats with kidney transplants to Lewis rats showed increased Tfh activity in both the graft and spleen, but the spleen's response was weaker, likely due to heightened Treg activation.
  • The findings suggest that different expressions of certain immune factors may explain the variations between the two tissues and could lead to improved treatments for CAN.

Article Abstract

The aim of this study was to investigate follicular helper T (Tfh) cell response and its difference between renal graft and spleen in a rat renal transplantation model undergoing chronic allograft nephropathy (CAN). Orthotopical kidney transplantations were performed on Fischer (F344) rats and transplanted to Lewis rats, using syngeneic Lewis-Lewis grafts as controls. Tissue samples were collected at 8 weeks posttransplantation. The status of Tfh cell response was assessed by measuring the levels of transcription factor B-cell lymphoma 6 (Bcl-6), interleukin-21 (IL-21), chemokine receptor type 5 (CXCR5), and B-cell-activating factor belonging to the TNF family (BAFF). Tfh cell response was upregulated in both renal graft and spleen of the CAN group compared to the control group. However, Tfh cell response of the spleen was weaker than that of the graft, which was possibly related to the upregulation of splenic Treg activation. Also, the difference between two tissues was partially associated with the different expressions of tristetraprolin (TTP)/IL-10. Our data help improve our understanding of the role of Tfh cell response in the body with CAN and may provide a valuable clue for better treatment of CAN.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5657687PMC
http://dx.doi.org/10.3727/096368916X692816DOI Listing

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