Expression of CD62L on Donor CD4+ T Cells in Allografts: Correlation with Graft-Versus-Host Disease after Unmanipulated Allogeneic Blood and Marrow Transplantation |
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Authors: | Ying-Jun Chang Xiang-Yu Zhao Ming-Rui Huo Xiao-Jun Huang |
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Affiliation: | (1) Peking University Institute of Hematology, Peking University People’s hospital, No 11 Xizhimen South Street, Beijing, 100044, China |
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Abstract: | Introduction The aim of this study was to investigate the association of donor CD4+ T cells expressing CD62L with transplant outcomes. Materials and Methods We report a prospective analysis of 31 patients who were treated with a Bu/Cy regimen, followed by unmanipulated blood and marrow transplantation. Results Median number (range) of CD4+CD62L+, CD4+CD45RA+CD62L+, and CD4+CD45RO+CD62L+ cells infused were 0.31(0.05–1.10)×108/kg, 0.22(0.03–0.95)× 108/kg, and 0.17(0.01–0.81)×108/kg, respectively. The incidence of grades II to IV aGVHD was 36%. In a multivariate analysis, infusion of >0.22 × 108 CD4+CD45RA+CD62L+ cells infused/kg increased the risk of grades II to IV aGVHD (HR = 4.741, 95% CI = 1.037–21.662, P = 0.045). Thirteen of 31 patients experienced cGVHD, the risk of cGVHD was increased in patients receiving >0.45 × 108 CD4+CD45RA+ cells infused/kg (HR = 4.614, 95% CI = 1.265–16.829, P = 0.021). Conclusion Our results suggest that a high cell dose of CD4+CD45RA+CD62L+ cells increase the incidence of grades II–IV aGVHD. A high number of CD4+CD45RA+ cells infused were associated with increased risk of cGVHD in our transplant settings. Ying-Jun Chang: performed research, analysis and interpretation of data, and drafting of the article, and gave final approval of the version to be published; Xiang-Yu Zhao: performed research, analysis and interpretation of data, and drafting of the article and gave final approval of the version to be published; Ming-Rui Huo: performed research, analysis and interpretation of data, and drafting of the article and gave final approval of the version to be published; Xiao-Jun Huang: involved in conception and design, revising the article critically, and final approval of the version to be published. |
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Keywords: | CD4+ cells graft-versus-host disease allogeneic blood and marrow transplantation CD62L |
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