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Low proportion of follicular regulatory T cell in renal transplant patients with chronic antibody-mediated rejection
Follicular regulatory T (Tfr) cell can effectively regulate humoral immunity, but its function and mechanism in antibody-mediated rejection (AMR) after organ transplantation remains unclear. Here we detected follicular helper T (Tfh) cell subsets in 88 renal transplant patients with chronic renal al...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431051/ https://www.ncbi.nlm.nih.gov/pubmed/28465534 http://dx.doi.org/10.1038/s41598-017-01625-3 |
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author | Chen, Wen Bai, Jian Huang, Haiyan Bi, Lili Kong, Xiangrui Gao, Yu Han, Yong Xiao, Li Shi, Bingyi |
author_facet | Chen, Wen Bai, Jian Huang, Haiyan Bi, Lili Kong, Xiangrui Gao, Yu Han, Yong Xiao, Li Shi, Bingyi |
author_sort | Chen, Wen |
collection | PubMed |
description | Follicular regulatory T (Tfr) cell can effectively regulate humoral immunity, but its function and mechanism in antibody-mediated rejection (AMR) after organ transplantation remains unclear. Here we detected follicular helper T (Tfh) cell subsets in 88 renal transplant patients with chronic renal allograft dysfunction (40 with AMR and 48 without AMR). The ratio of Tfr cells in renal graft tissues and peripheral blood of AMR patients significantly decreased, while the ratio of IL-21-producing Tfh cells (Tfh2 and Tfh17) significantly increased, compared to non-AMR patients. When tested in functional assays, Tfr cells from both AMR and non-AMR patients exerted equivalent inhibitory function. Tfr cell transplantation or CTLA-4 virus transfection could significantly inhibit IL-21 secretion from Tfh cells of these patients, further suppress the proliferation and differentiation of B cells. CTLA-4 blocking, IL-10 and TGF-β neutralization could partially weaken such inhibitory effect of Tfr cells. Besides, our study found that sirolimus reduced the ratio of Tfr cells, while cyclosporine and tacrolimus had no significant effect on Tfr cells. In a word, renal transplant patients with AMR have low proportion of Tfr cells but these cell exerted normal function. |
format | Online Article Text |
id | pubmed-5431051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54310512017-05-16 Low proportion of follicular regulatory T cell in renal transplant patients with chronic antibody-mediated rejection Chen, Wen Bai, Jian Huang, Haiyan Bi, Lili Kong, Xiangrui Gao, Yu Han, Yong Xiao, Li Shi, Bingyi Sci Rep Article Follicular regulatory T (Tfr) cell can effectively regulate humoral immunity, but its function and mechanism in antibody-mediated rejection (AMR) after organ transplantation remains unclear. Here we detected follicular helper T (Tfh) cell subsets in 88 renal transplant patients with chronic renal allograft dysfunction (40 with AMR and 48 without AMR). The ratio of Tfr cells in renal graft tissues and peripheral blood of AMR patients significantly decreased, while the ratio of IL-21-producing Tfh cells (Tfh2 and Tfh17) significantly increased, compared to non-AMR patients. When tested in functional assays, Tfr cells from both AMR and non-AMR patients exerted equivalent inhibitory function. Tfr cell transplantation or CTLA-4 virus transfection could significantly inhibit IL-21 secretion from Tfh cells of these patients, further suppress the proliferation and differentiation of B cells. CTLA-4 blocking, IL-10 and TGF-β neutralization could partially weaken such inhibitory effect of Tfr cells. Besides, our study found that sirolimus reduced the ratio of Tfr cells, while cyclosporine and tacrolimus had no significant effect on Tfr cells. In a word, renal transplant patients with AMR have low proportion of Tfr cells but these cell exerted normal function. Nature Publishing Group UK 2017-05-02 /pmc/articles/PMC5431051/ /pubmed/28465534 http://dx.doi.org/10.1038/s41598-017-01625-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, Wen Bai, Jian Huang, Haiyan Bi, Lili Kong, Xiangrui Gao, Yu Han, Yong Xiao, Li Shi, Bingyi Low proportion of follicular regulatory T cell in renal transplant patients with chronic antibody-mediated rejection |
title | Low proportion of follicular regulatory T cell in renal transplant patients with chronic antibody-mediated rejection |
title_full | Low proportion of follicular regulatory T cell in renal transplant patients with chronic antibody-mediated rejection |
title_fullStr | Low proportion of follicular regulatory T cell in renal transplant patients with chronic antibody-mediated rejection |
title_full_unstemmed | Low proportion of follicular regulatory T cell in renal transplant patients with chronic antibody-mediated rejection |
title_short | Low proportion of follicular regulatory T cell in renal transplant patients with chronic antibody-mediated rejection |
title_sort | low proportion of follicular regulatory t cell in renal transplant patients with chronic antibody-mediated rejection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431051/ https://www.ncbi.nlm.nih.gov/pubmed/28465534 http://dx.doi.org/10.1038/s41598-017-01625-3 |
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