Association of epstein–barr virus reactivation with the recovery of cd4/cd8 double-negative t lymphocytes after haploidentical hematopoietic stem cell transplantation

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Association of epstein–barr virus reactivation with the recovery of cd4/cd8 double-negative t lymphocytes after haploidentical hematopoietic stem cell transplantation"


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ABSTRACT EBV infection is one of the life-threatening clinical complications in patients who underwent haploidentical hematopoietic stem cell transplantation (haploHSCT). Although immune


recovery is recognized to be crucial for decreasing subsequent morbidity of infections, the link between T-cell recovery and EBV infection after haploHSCT remains elusive. We recently


compared the influences of different doses of antithymocyte globulin conditioning on the T-cell reconstitution post haploHSCT and suggested that CD4−CD8−T cells might interact with the


occurrence of EBV reactivation. In the current study, haploHSCT recipients with EBV-DNAemia (_n_=64) were compared with a control group without EBV reactivation (_n_=192), with regard to the


recoveries of T-cell subpopulations. In contrast to other T-cell subpopulations, the median counts ofCD4−CD8−T cells in recipients with EBV-DNAemia were significantly lower than the control


group at a serial time course (30, 90 and 180 days) after transplantation. Landmark studies further confirmed the correlation of CD4−CD8−T cells with the EBV infection. Multivariate


analysis showed that hampered recovery of CD4−CD8−T cells and EBV reactivation were the independent risk factors to predict transplant-related mortality. Our findings may facilitate the


intervention strategies to improve the overall survival of haploHSCT recipients. Access through your institution Buy or subscribe This is a preview of subscription content, access via your


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RECEPTOR-LIGAND-MISMATCHED CORD BLOOD TRANSPLANTATION Article 08 January 2021 SECONDARY BONE MARROW GRAFT LOSS AFTER THIRD-PARTY VIRUS-SPECIFIC T CELL INFUSION: CASE REPORT OF A RARE


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potential pinch hitters in the T-cell lineup. _Curr Opin HIV AIDS_ 2012; 7: 164–171. Article  CAS  Google Scholar  Download references ACKNOWLEDGEMENTS This study is supported by Key Program


of the National Natural Science Foundation of China (Grant No 81230013) and National Natural Science Foundation of China (Grant No. 81370666). AUTHOR INFORMATION Author notes * Z Bian and J


Liu: These authors contributed equally to this work. AUTHORS AND AFFILIATIONS * Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key laboratory


of Hematopoietic Stem Cell Transplantation, Beijing, China Z Bian, J Liu, L-P Xu, Y-J Chang, Y Wang, X-H Zhang & X-J Huang Authors * Z Bian View author publications You can also search


for this author inPubMed Google Scholar * J Liu View author publications You can also search for this author inPubMed Google Scholar * L-P Xu View author publications You can also search for


this author inPubMed Google Scholar * Y-J Chang View author publications You can also search for this author inPubMed Google Scholar * Y Wang View author publications You can also search


for this author inPubMed Google Scholar * X-H Zhang View author publications You can also search for this author inPubMed Google Scholar * X-J Huang View author publications You can also


search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to X-J Huang. ETHICS DECLARATIONS COMPETING INTERESTS The authors declare no conflict of interest. RIGHTS


AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Bian, Z., Liu, J., Xu, LP. _et al._ Association of Epstein–Barr virus reactivation with the recovery of CD4/CD8


double-negative T lymphocytes after haploidentical hematopoietic stem cell transplantation. _Bone Marrow Transplant_ 52, 264–269 (2017). https://doi.org/10.1038/bmt.2016.238 Download


citation * Received: 18 April 2016 * Revised: 20 July 2016 * Accepted: 07 August 2016 * Published: 31 October 2016 * Issue Date: February 2017 * DOI: https://doi.org/10.1038/bmt.2016.238


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