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- Publisher Website: 10.1038/sj.bmt.1704566
- Scopus: eid_2-s2.0-4344652822
- PMID: 15195076
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Article: Antirecipient helper and cytotoxic T-cell frequencies in bone marrow transplantation
Title | Antirecipient helper and cytotoxic T-cell frequencies in bone marrow transplantation |
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Authors | |
Keywords | Cytotoxic T-lymphocytes precursor frequency Graft-versus-host disease Helper T-cell precursor frequency IFN-γ-producing cell frequency Limiting dilution assay |
Issue Date | 2004 |
Publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/bmt |
Citation | Bone Marrow Transplantation, 2004, v. 34 n. 3, p. 207-213 How to Cite? |
Abstract | We assayed helper T-lymphocyte precursor frequencies (HTLPf), interferon (IFN)-γ-producing cell frequencies (IFN-γPf) and CTL precursor frequencies (CTLPf) to see if they could predict the severity of acute graft-versus-host disease (aGVHD) and disease relapse after transplantation. In all, 48 bone marrow transplantation (BMT) patients and their HLA-identical sibling (n = 29) or matched unrelated donors (MUD) (n = 19) were recruited. HTLPf, IFN-γPf and CTLPf were measured using a limiting dilution assay (LDA). Patients were followed prospectively to assess the severity of aGVHD and the status of the primary disease after BMT. High (>5 × 10-6) HTLPf, CTLPf and IFN-γPf were significantly associated with the occurrence and severity of aGVHD in patients who received transplants from HLA-identical sibling. Among patients receiving BMT from MUD, HTLPf and CTLPf, but not IFN-γPf, were associated with aGVHD. Five patients had disease relapse post-BMT and the risk was not significantly associated with HTLPf CTLPf or IFN-γPf. Patients with high (>5 × 10-6) HTLPf, IFN-γPf or CTLPf before BMT are at higher risk of developing aGVHD after transplantation from both matched sibling donors and MUD. Whether these parameters can predict disease relapse would have to be investigated with a larger cohort of patients. © 2004 Nature Publishing Group All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/77378 |
ISSN | 2023 Impact Factor: 4.5 2023 SCImago Journal Rankings: 1.318 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kwok, JSY | en_HK |
dc.contributor.author | Leung, AYH | en_HK |
dc.contributor.author | Lie, AKW | en_HK |
dc.contributor.author | Lee, TL | en_HK |
dc.contributor.author | Lau, YL | en_HK |
dc.contributor.author | Chu, P | en_HK |
dc.contributor.author | Jones, B | en_HK |
dc.contributor.author | Hawkins, B | en_HK |
dc.contributor.author | Liang, R | en_HK |
dc.date.accessioned | 2010-09-06T07:31:15Z | - |
dc.date.available | 2010-09-06T07:31:15Z | - |
dc.date.issued | 2004 | en_HK |
dc.identifier.citation | Bone Marrow Transplantation, 2004, v. 34 n. 3, p. 207-213 | en_HK |
dc.identifier.issn | 0268-3369 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77378 | - |
dc.description.abstract | We assayed helper T-lymphocyte precursor frequencies (HTLPf), interferon (IFN)-γ-producing cell frequencies (IFN-γPf) and CTL precursor frequencies (CTLPf) to see if they could predict the severity of acute graft-versus-host disease (aGVHD) and disease relapse after transplantation. In all, 48 bone marrow transplantation (BMT) patients and their HLA-identical sibling (n = 29) or matched unrelated donors (MUD) (n = 19) were recruited. HTLPf, IFN-γPf and CTLPf were measured using a limiting dilution assay (LDA). Patients were followed prospectively to assess the severity of aGVHD and the status of the primary disease after BMT. High (>5 × 10-6) HTLPf, CTLPf and IFN-γPf were significantly associated with the occurrence and severity of aGVHD in patients who received transplants from HLA-identical sibling. Among patients receiving BMT from MUD, HTLPf and CTLPf, but not IFN-γPf, were associated with aGVHD. Five patients had disease relapse post-BMT and the risk was not significantly associated with HTLPf CTLPf or IFN-γPf. Patients with high (>5 × 10-6) HTLPf, IFN-γPf or CTLPf before BMT are at higher risk of developing aGVHD after transplantation from both matched sibling donors and MUD. Whether these parameters can predict disease relapse would have to be investigated with a larger cohort of patients. © 2004 Nature Publishing Group All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/bmt | en_HK |
dc.relation.ispartof | Bone Marrow Transplantation | en_HK |
dc.subject | Cytotoxic T-lymphocytes precursor frequency | en_HK |
dc.subject | Graft-versus-host disease | en_HK |
dc.subject | Helper T-cell precursor frequency | en_HK |
dc.subject | IFN-γ-producing cell frequency | en_HK |
dc.subject | Limiting dilution assay | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Bone Marrow Transplantation - immunology | en_HK |
dc.subject.mesh | Child | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Graft vs Host Disease - immunology | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Retrospective Studies | en_HK |
dc.subject.mesh | T-Lymphocytes, Cytotoxic - immunology | en_HK |
dc.subject.mesh | T-Lymphocytes, Helper-Inducer - immunology | en_HK |
dc.title | Antirecipient helper and cytotoxic T-cell frequencies in bone marrow transplantation | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0268-3369&volume=34&issue=3&spage=207&epage=213&date=2004&atitle=Antirecipient+helper+and+cytotoxic+T-cell+frequencies+in+bone+marrow+transplantation | en_HK |
dc.identifier.email | Leung, AYH:ayhleung@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 | Leung, AYH=rp00265 | en_HK |
dc.identifier.authority | Lau, YL=rp00361 | en_HK |
dc.identifier.authority | Liang, R=rp00345 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1038/sj.bmt.1704566 | en_HK |
dc.identifier.pmid | 15195076 | - |
dc.identifier.scopus | eid_2-s2.0-4344652822 | en_HK |
dc.identifier.hkuros | 99041 | en_HK |
dc.identifier.hkuros | 95096 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-4344652822&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 34 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 207 | en_HK |
dc.identifier.epage | 213 | en_HK |
dc.identifier.isi | WOS:000222725800003 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Kwok, JSY=7006208874 | en_HK |
dc.identifier.scopusauthorid | Leung, AYH=7403012668 | en_HK |
dc.identifier.scopusauthorid | Lie, AKW=24284842400 | en_HK |
dc.identifier.scopusauthorid | Lee, TL=24483772800 | en_HK |
dc.identifier.scopusauthorid | Lau, YL=7201403380 | en_HK |
dc.identifier.scopusauthorid | Chu, P=7402159699 | en_HK |
dc.identifier.scopusauthorid | Jones, B=7404958958 | en_HK |
dc.identifier.scopusauthorid | Hawkins, B=35944486200 | en_HK |
dc.identifier.scopusauthorid | Liang, R=26643224900 | en_HK |
dc.identifier.issnl | 0268-3369 | - |