CMV infection combined with acute GVHD associated with poor CD8+ T-cell immune reconstitution and poor prognosis post-HLA-matched allo-HSCT

Author:

Fan Ze-Ying1ORCID,Han Ting-Ting1,Zuo Wei1,Zhao Xiao-Su1,Chang Ying-Jun1,Lv Meng1,Mo Xiao-Dong1,Sun Yu-Qian1,Zhang Yuan-Yuan1,Wang Yu1,Xu Lan-Ping1,Zhang Xiao-Hui1,Liu Kai-Yan1,Huang Xiao-Jun1,Zhao Xiang-Yu12ORCID

Affiliation:

1. Peking University People’s Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation , Beijing 100044 , China

2. Collaborative Innovation Center of Hematology , Beijing 100044 , China

Abstract

Abstract Cytomegalovirus (CMV) infection and acute graft-versus-host disease (aGVHD) are two major complications that contribute to a poor prognosis after hematopoietic stem cell transplantation (HSCT). Superior early immune reconstitution (IR) is associated with improved survival after HSCT. However, when all three factors, CMV infection, aGVHD, and IR, are concomitantly considered, the effects of the triple events on HSCT are still unknown and should be studied further. Thus we enrolled 185 patients who were diagnosed as hematological malignancies and treated with HLA-matched sibling transplantation (MST) between January 2010 and December 2014, of whom 83 were positive for CMV infection and 82 had aGVHD. Results showed that patients with both aGVHD and CMV infection had significantly higher non-relapse mortality (NRM), lower overall survival (OS), and delayed CD8+ T-cell IR. Multivariate analyses showed that both aGVHD combined with CMV infection and delayed CD8+ T-cell IR were independent risk factors for prognosis post-MST. Recurrent CMV infections are associated with poor CD8+ T-cell reconstitution. However, superior IR could protect against the negative effects of aGVHD and CMV infection on the transplant outcomes.

Funder

Beijing Municipal Science and Technology Commission

National Natural Science Foundation of China

Peking University People’s Hospital Research and Development Funds

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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