Human Herpesvirus 6 Reactivation Evaluated by Digital Polymerase Chain Reaction and Its Association With Dynamics of CD134-Positive T Cells After Allogeneic Hematopoietic Stem Cell Transplantation

Author:

Nakayama Hitomi1ORCID,Yamazaki Rie12,Kato Jun1,Koda Yuya1,Sakurai Masatoshi1,Abe Ryohei1,Watanuki Shintaro1,Sumiya Chieko1,Shiroshita Kohei1,Fujita Shinya1,Yamaguchi Kentaro1,Okamoto Shinichiro1,Mori Takehiko1

Affiliation:

1. Division of Hematology, Department of Medicine, Tokyo, Japan

2. Center for Transfusion Medicine and Cell Therapy, Keio University School of Medicine, Tokyo, Japan

Abstract

AbstractBackgroundHuman herpesvirus 6 (HHV-6) causes life-threatening central nervous system disorders after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Recent studies implicated CD134 as a specific receptor of HHV-6B and demonstrated that its expression levels in CD4-positive T cells after allo-HSCT could be related to the reactivation of HHV-6. We prospectively evaluated the relationship between HHV-6 reactivation and CD134+ T cells in the recipients of allo-HSCT.MethodsHHV-6 viral load in plasma was quantitatively measured weekly after allo-HSCT by digital polymerase chain reaction in 34 patients. The ratio of CD134 in CD4+ T cells (CD134/CD4 ratio) was serially measured by flow cytometry before and after transplantation.ResultsHHV-6 reactivation was detected in 23 patients (68%). The CD134/CD4 ratio before conditioning was significantly higher in patients with HHV-6 reactivation than in those without (median, 3.8% vs 1.5%, P < .01). In multivariate analysis, a higher CD134/CD4 ratio before conditioning was significantly associated with the incidence of HHV-6 reactivation (odds ratio, 10.5 [95% confidence interval, 1.3–85.1], P = .03).ConclusionsA higher CD134/CD4 ratio before conditioning was associated with a higher risk of HHV-6 reactivation, suggesting that the rate may be a promising marker for predicting HHV-6 reactivation after allo-HSCT.

Funder

Japan Society

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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