Phenotype and molecular signature of CD8(+) T cell subsets in T cell- mediated rejections after kidney transplantation

We investigated the phenotype and molecular signatures of CD8(+)T cell subsets in kidney-transplant recipients (KTRs) with biopsy-proven T cell-mediated rejection (TCMR). We included 121 KTRs and divided them into three groups according to the pathologic or clinical diagnosis: Normal biopsy control...

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Veröffentlicht in:PloS one 2020-06, Vol.15 (6), p.e0234323-e0234323, Article 0234323
Hauptverfasser: Ko, Eun Jeong, Seo, Jung-Woo, Kim, Kyoung Woon, Kim, Bo-Mi, Cho, Jang-Hee, Kim, Chan-Duck, Seok, Junhee, Yang, Chul Woo, Lee, Sang-Ho, Chung, Byung Ha
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Sprache:eng
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Zusammenfassung:We investigated the phenotype and molecular signatures of CD8(+)T cell subsets in kidney-transplant recipients (KTRs) with biopsy-proven T cell-mediated rejection (TCMR). We included 121 KTRs and divided them into three groups according to the pathologic or clinical diagnosis: Normal biopsy control (NC)(n= 32), TCMR (n= 50), and long-term graft survival (LTGS)(n= 39). We used flowcytometry and microarray to analyze the phenotype and molecular signatures of CD8(+)T cell subsets using peripheral blood from those patients and analyzed significant gene expressions according to CD8(+)T cell subsets. We investigated whether the analysis of CD8(+)T cell subsets is useful for predicting the development of TCMR. CCR7(+)CD8(+)T cells significantly decreased, but CD28(null)CD57(+)CD8(+)T cells and CCR7(-)CD45RA(+)CD8(+)T cells showed an increase in the TCMR group compared to other groups (p
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0234323