Is there a role for B lymphocyte chimerism in the monitoring of B-acute lymphoblastic leukemia patients receiving allogeneic stem cell transplantation?

Objective: To determine the sensitivity and significance of B-cell chimerism for the detection of early engraftment, transplant rejection, and disease relapse. Methods: The dynamic monitoring of lineage-specific cell subtypes (B, T, and NK cells) was made in 20 B-cell acute lymphoblastic leukemia (B...

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Main Authors: Yi-Ning Yang, Xiao-Rui Wang, You-Wen Qin, Li-Ping Wan, Ying Jiang, Chun Wang
Format: Article
Language:English
Published: Wiley 2015-03-01
Series:Chronic Diseases and Translational Medicine
Online Access:http://www.sciencedirect.com/science/article/pii/S2095882X15000055
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author Yi-Ning Yang
Xiao-Rui Wang
You-Wen Qin
Li-Ping Wan
Ying Jiang
Chun Wang
author_facet Yi-Ning Yang
Xiao-Rui Wang
You-Wen Qin
Li-Ping Wan
Ying Jiang
Chun Wang
author_sort Yi-Ning Yang
collection DOAJ
description Objective: To determine the sensitivity and significance of B-cell chimerism for the detection of early engraftment, transplant rejection, and disease relapse. Methods: The dynamic monitoring of lineage-specific cell subtypes (B, T, and NK cells) was made in 20 B-cell acute lymphoblastic leukemia (B-ALL) patients following allogeneic hematopoietic stem cell transplantation (allo-HSCT). In the early period after allo-HSCT, the latest establishment of B-cell complete chimerism (CC) was observed in a majority of patients. Results: The percentage of donor cells of B-cell lineage was lower than the percent of T-cell lineage in most of the mixed chimerism (MC) patients. During graft rejection, the frequency of patients with decreasing MC of B-, T- and NK-cell lineage were 5/5, 2/5, and 2/5. When disease relapsed, five patients showed a faster decrease of the donor percent of B-cells than of T- or NK-cells. Only one patient displayed a more rapid decrease in NK-cells than in T- or B-cells. Conclusion: Monitoring of B-cell chimerism after HSCT seems to be valuable for insuring complete engraftment, anticipating graft rejection, and relapse in B-ALL patients. Keywords: B cell acute lymphoblastic leukemia (B-ALL), B-cell, T-cell, Chimerism, Allogeneic hematopoietic stem cell transplantation (allo-HSCT)
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spelling doaj.art-00ebe62a75014ea78d576a7d41fd23212022-12-22T02:46:21ZengWileyChronic Diseases and Translational Medicine2095-882X2015-03-01114854Is there a role for B lymphocyte chimerism in the monitoring of B-acute lymphoblastic leukemia patients receiving allogeneic stem cell transplantation?Yi-Ning Yang0Xiao-Rui Wang1You-Wen Qin2Li-Ping Wan3Ying Jiang4Chun Wang5Department of Hematology, Shanghai Jiao Tong University affiliated with Shanghai General Hospital, Shanghai 200000, ChinaDepartment of Hematology, Shanghai Jiao Tong University affiliated with Shanghai General Hospital, Shanghai 200000, ChinaCorresponding author.; Department of Hematology, Shanghai Jiao Tong University affiliated with Shanghai General Hospital, Shanghai 200000, ChinaDepartment of Hematology, Shanghai Jiao Tong University affiliated with Shanghai General Hospital, Shanghai 200000, ChinaDepartment of Hematology, Shanghai Jiao Tong University affiliated with Shanghai General Hospital, Shanghai 200000, ChinaDepartment of Hematology, Shanghai Jiao Tong University affiliated with Shanghai General Hospital, Shanghai 200000, ChinaObjective: To determine the sensitivity and significance of B-cell chimerism for the detection of early engraftment, transplant rejection, and disease relapse. Methods: The dynamic monitoring of lineage-specific cell subtypes (B, T, and NK cells) was made in 20 B-cell acute lymphoblastic leukemia (B-ALL) patients following allogeneic hematopoietic stem cell transplantation (allo-HSCT). In the early period after allo-HSCT, the latest establishment of B-cell complete chimerism (CC) was observed in a majority of patients. Results: The percentage of donor cells of B-cell lineage was lower than the percent of T-cell lineage in most of the mixed chimerism (MC) patients. During graft rejection, the frequency of patients with decreasing MC of B-, T- and NK-cell lineage were 5/5, 2/5, and 2/5. When disease relapsed, five patients showed a faster decrease of the donor percent of B-cells than of T- or NK-cells. Only one patient displayed a more rapid decrease in NK-cells than in T- or B-cells. Conclusion: Monitoring of B-cell chimerism after HSCT seems to be valuable for insuring complete engraftment, anticipating graft rejection, and relapse in B-ALL patients. Keywords: B cell acute lymphoblastic leukemia (B-ALL), B-cell, T-cell, Chimerism, Allogeneic hematopoietic stem cell transplantation (allo-HSCT)http://www.sciencedirect.com/science/article/pii/S2095882X15000055
spellingShingle Yi-Ning Yang
Xiao-Rui Wang
You-Wen Qin
Li-Ping Wan
Ying Jiang
Chun Wang
Is there a role for B lymphocyte chimerism in the monitoring of B-acute lymphoblastic leukemia patients receiving allogeneic stem cell transplantation?
Chronic Diseases and Translational Medicine
title Is there a role for B lymphocyte chimerism in the monitoring of B-acute lymphoblastic leukemia patients receiving allogeneic stem cell transplantation?
title_full Is there a role for B lymphocyte chimerism in the monitoring of B-acute lymphoblastic leukemia patients receiving allogeneic stem cell transplantation?
title_fullStr Is there a role for B lymphocyte chimerism in the monitoring of B-acute lymphoblastic leukemia patients receiving allogeneic stem cell transplantation?
title_full_unstemmed Is there a role for B lymphocyte chimerism in the monitoring of B-acute lymphoblastic leukemia patients receiving allogeneic stem cell transplantation?
title_short Is there a role for B lymphocyte chimerism in the monitoring of B-acute lymphoblastic leukemia patients receiving allogeneic stem cell transplantation?
title_sort is there a role for b lymphocyte chimerism in the monitoring of b acute lymphoblastic leukemia patients receiving allogeneic stem cell transplantation
url http://www.sciencedirect.com/science/article/pii/S2095882X15000055
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