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Article: A case-controlled study on the use of HBsAg-positive donors for allogeneic hematopoietic cell transplantation
Title | A case-controlled study on the use of HBsAg-positive donors for allogeneic hematopoietic cell transplantation |
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Authors | |
Issue Date | 2000 |
Publisher | American Society of Hematology. The Journal's web site is located at http://bloodjournal.hematologylibrary.org/ |
Citation | Blood, 2000, v. 96 n. 2, p. 452-458 How to Cite? |
Abstract | To compare the clinical and serological outcomes of patients receiving donors' marrow positive or negative for hepatitis B surface antigen (HBsAg), we studied 18 patients of allogeneic hematopoietic cell transplantation receiving HBsAg-positive marrow (group 1) and 18 receiving HBsAg-negative marrow (group 2). The recipients of the 2 groups were matched for hepatitis B virus (HBV) serology, sex, age, underlying hematological diseases, conditioning regimen, and prophylaxis against graft-versus-host diseases. Eight (44.4%) recipients in group 1 and 2 (11.1%) in group 2 suffered from HBV- related hepatitis posttransplant (P = .03). Furthermore, HBV-related hepatic failure was seen in 6 group 1 patients, but in none of the group 2 patients (P = .007). Five of the 9 (55.5%) HBsAg-negative recipients in group 1 became positive after receiving HBsAg-positive marrow. Serum HBV DNA was positive in all 5 donors of these patients, but in none of the donors of recipients who remained HBsAg negative (P = .008). Group 1 patients developing HBV-related hepatitis posttransplant were more likely to have a donor carrying a precore A 1896 and/or core promoter T 1762/A 1764 HBV variant (62.5% versus 0%, P = .007). This study has demonstrated that a high incidence of HBV-related hepatitis was associated with the use of HBsAg- positive marrow for transplant, and a high viral load in the donor appeared to predispose recipients to the development of HBV-related hepatitis posttransplant. Further clinical trials will be necessary to determine the optimal management approach to this problem, including the use of the antiviral agents in the donors and the recipients. (C) 2000 by The American Society of Hematology. |
Persistent Identifier | http://hdl.handle.net/10722/77032 |
ISSN | 2023 Impact Factor: 21.0 2023 SCImago Journal Rankings: 5.272 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lau, GKK | en_HK |
dc.contributor.author | Lie, AKW | en_HK |
dc.contributor.author | Kwong, YL | en_HK |
dc.contributor.author | Lee, CK | en_HK |
dc.contributor.author | Hou, J | en_HK |
dc.contributor.author | Lau, YL | en_HK |
dc.contributor.author | Lim, WL | en_HK |
dc.contributor.author | Liang, R | en_HK |
dc.date.accessioned | 2010-09-06T07:27:32Z | - |
dc.date.available | 2010-09-06T07:27:32Z | - |
dc.date.issued | 2000 | en_HK |
dc.identifier.citation | Blood, 2000, v. 96 n. 2, p. 452-458 | en_HK |
dc.identifier.issn | 0006-4971 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77032 | - |
dc.description.abstract | To compare the clinical and serological outcomes of patients receiving donors' marrow positive or negative for hepatitis B surface antigen (HBsAg), we studied 18 patients of allogeneic hematopoietic cell transplantation receiving HBsAg-positive marrow (group 1) and 18 receiving HBsAg-negative marrow (group 2). The recipients of the 2 groups were matched for hepatitis B virus (HBV) serology, sex, age, underlying hematological diseases, conditioning regimen, and prophylaxis against graft-versus-host diseases. Eight (44.4%) recipients in group 1 and 2 (11.1%) in group 2 suffered from HBV- related hepatitis posttransplant (P = .03). Furthermore, HBV-related hepatic failure was seen in 6 group 1 patients, but in none of the group 2 patients (P = .007). Five of the 9 (55.5%) HBsAg-negative recipients in group 1 became positive after receiving HBsAg-positive marrow. Serum HBV DNA was positive in all 5 donors of these patients, but in none of the donors of recipients who remained HBsAg negative (P = .008). Group 1 patients developing HBV-related hepatitis posttransplant were more likely to have a donor carrying a precore A 1896 and/or core promoter T 1762/A 1764 HBV variant (62.5% versus 0%, P = .007). This study has demonstrated that a high incidence of HBV-related hepatitis was associated with the use of HBsAg- positive marrow for transplant, and a high viral load in the donor appeared to predispose recipients to the development of HBV-related hepatitis posttransplant. Further clinical trials will be necessary to determine the optimal management approach to this problem, including the use of the antiviral agents in the donors and the recipients. (C) 2000 by The American Society of Hematology. | en_HK |
dc.language | eng | en_HK |
dc.publisher | American Society of Hematology. The Journal's web site is located at http://bloodjournal.hematologylibrary.org/ | en_HK |
dc.relation.ispartof | Blood | en_HK |
dc.subject.mesh | Adolescent | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Bone Marrow Cells - virology | en_HK |
dc.subject.mesh | Case-Control Studies | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Hematopoietic Stem Cell Transplantation | en_HK |
dc.subject.mesh | Hepatitis B - etiology - mortality | en_HK |
dc.subject.mesh | Hepatitis B Antibodies - blood | en_HK |
dc.subject.mesh | Hepatitis B Surface Antigens - analysis | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Tissue Donors | en_HK |
dc.title | A case-controlled study on the use of HBsAg-positive donors for allogeneic hematopoietic cell transplantation | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0006-4971&volume=96&issue=2&spage=452&epage=458&date=2000&atitle=A+case-controlled+study+on+the+use+of+HBsAg-positive+donors+for+allogeneic+hematopoietic+cell+transplantation | en_HK |
dc.identifier.email | Kwong, YL:ylkwong@hku.hk | en_HK |
dc.identifier.email | Lau, YL:lauylung@hkucc.hku.hk | en_HK |
dc.identifier.email | Liang, R:rliang@hku.hk | en_HK |
dc.identifier.authority | Kwong, YL=rp00358 | en_HK |
dc.identifier.authority | Lau, YL=rp00361 | en_HK |
dc.identifier.authority | Liang, R=rp00345 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.pmid | 10887105 | - |
dc.identifier.scopus | eid_2-s2.0-0034661838 | en_HK |
dc.identifier.hkuros | 55820 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0034661838&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 96 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 452 | en_HK |
dc.identifier.epage | 458 | en_HK |
dc.identifier.isi | WOS:000088234800011 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Lau, GKK=7102301257 | en_HK |
dc.identifier.scopusauthorid | Lie, AKW=24284842400 | en_HK |
dc.identifier.scopusauthorid | Kwong, YL=7102818954 | en_HK |
dc.identifier.scopusauthorid | Lee, CK=36087620900 | en_HK |
dc.identifier.scopusauthorid | Hou, J=7401966390 | en_HK |
dc.identifier.scopusauthorid | Lau, YL=7201403380 | en_HK |
dc.identifier.scopusauthorid | Lim, WL=24492170000 | en_HK |
dc.identifier.scopusauthorid | Liang, R=26643224900 | en_HK |
dc.identifier.issnl | 0006-4971 | - |