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Updated: Dec 27, 2025
In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
Analysis of Immune Cell Repopulation After Anti-thymocyte Globulin Administration for Steroid-Resistant
Ji Hyun Sim1, Seung Seok Han2, Dong-Sup Lee3
1Department of Anatomy and Cell Biology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Background:
Anti-thymocyte globulin (ATG) is a treatment option for steroid-resistant T-cell-mediated rejection after kidney transplantation. However, the extent to which immune-cell subsets can repopulate the peripheral blood is unknown.
Methods:
Six patients with steroid-resistant T-cell-mediated rejection were recruited and underwent analysis of their immune cells for 1 year after ATG administration. Multicolor flow cytometric analysis was used to evaluate the proportions of T cells, B cells, natural killer cells, and monocytes.
Results:
T-cell repopulation from 24% to 75% occurred in the treatment group. The major repopulated cells were effector memory CD8+ T cells followed by effector memory CD4+ T cells. The population of effector memory CD8+ T cells with low expression of interleukin-7 receptor α increased over time. The population of regulatory T cells (eg, CD8+CD28-CD56+ T cells and CD4+CD25bright T cells) increased after ATG administration. However, the populations of other immune-cell subsets, including B cells, natural killer cells, and monocytes, were not significantly altered by ATG.
Conclusions:
Our findings on immune cell repopulation after ATG administration will enable future studies aiming to unravel the steroid-resistance mechanism underlying T-cell-mediated rejection.
