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Pretransplant CD28 Biomarker (Levels of Expression and Quantification of Molecules per Cell) in Peripheral CD4 + T Cells Predicts Acute Rejection Episodes in Liver and Kidney Recipients.

Authors :
Boix F
Bolarín JM
Eguía J
Gonzalez-Martinez G
De La Peña J
Galian JA
Hernández-Martínez AM
Moya-Quiles MR
Legaz I
Campillo JA
Ramirez P
Sanchez-Bueno F
García-Alonso AM
Pons JA
Minguela A
Llorente S
Muro M
Source :
Transplantation proceedings [Transplant Proc] 2016 Nov; Vol. 48 (9), pp. 2987-2989.
Publication Year :
2016

Abstract

Background: Acute rejection (AR) remains a significant cause of graft loss. Better approaches to predict AR are being investigated. Surface CD28 protein is essential for T-cell proliferation and survival as well as cytokine production.<br />Patients and Methods: Pretransplant CD4 <superscript>+</superscript> CD28 <superscript>+</superscript> peripheral T cells were examined in 30 liver recipients (LRs) and 31 kidney recipients (KRs) by flow cytometry.<br />Results: Pretransplant CD4 <superscript>+</superscript> CD28 <superscript>+</superscript> T cells in LRs were significantly lower in rejectors than nonrejectors (P = .002). Furthermore, the total number of CD28 molecules per cell in LRs (P = .02) as well as KRs (P = .047) was significantly lower in rejectors than nonrejectors. The healthy group did not display differences when compared with patients with end-stage liver disease or renal failure; however, stratification analysis displayed higher levels of CD4 <superscript>+</superscript> CD28 <superscript>+</superscript> when compared with rejected LRs (P = .04) but not KRs. CD28 levels <41.94% were able to discriminate LRs at high risk of AR (P = .003). Similarly, a total number of CD28 molecules ≤8359 (P = .031) in LRs and ≤7669 (P = .046) in KRs correlated with high risk of AR.<br />Conclusion: The preliminary results presented herein exhibit a fast and noninvasive method that assists clinicians to prevent AR by monitoring CD4 <superscript>+</superscript> CD28 <superscript>+</superscript> peripheral T cells.<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-2623
Volume :
48
Issue :
9
Database :
MEDLINE
Journal :
Transplantation proceedings
Publication Type :
Academic Journal
Accession number :
27932126
Full Text :
https://doi.org/10.1016/j.transproceed.2016.09.028