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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0005961,
umls-concept:C0013018,
umls-concept:C0039195,
umls-concept:C0042960,
umls-concept:C0376249,
umls-concept:C0445356,
umls-concept:C0936012,
umls-concept:C1449559,
umls-concept:C1522609,
umls-concept:C1527169,
umls-concept:C1549078,
umls-concept:C1554112,
umls-concept:C1709634,
umls-concept:C1997894
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pubmed:issue |
9
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pubmed:dateCreated |
1995-6-27
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pubmed:abstractText |
Between May 1989 and February 1994, we performed 48 volunteer unrelated donor BMTs for first chronic phase chronic myeloid leukemia using in vivo T cell depletion for acute graft-versus-host disease (aGvHD) prophylaxis. In 40 cases, adequate material was available to measure the frequency of antirecipient MHC cytotoxic T lymphocyte precursor (CTLp) cells in the blood of potential donors. This supplemented standard serological typing, one-dimensional isoelectric focusing for class I proteins, and allogenotyping for DR and DQ alleles using DNA RFLP analysis in the donor selection process. All recipients were conditioned with cyclophosphamide 120 mg/kg, TBI 1320 cGy, and intravenous Campath 1G. GvHD prophylaxis consisted of CsA, short-course methotrexate, and intravenous Campath 1G. Minimum follow-up in all surviving recipients was 100 days. The development of aGvHD and the probability of leukemia-free survival were compared between the high frequency group (CTLp > 1 in 100,000) (n = 15) and the low frequency group (CTLp < 1 in 100,000) (n = 25). There was a trend for increasing grade of aGvHD, which was statistically significant in the high frequency group when compared with the low frequency group (P = 0.003). Both a high frequency of CTLp (relative risk [RR] = 9.0, P = 0.016) and HLA mismatch (RR = 6.7, P = 0.023) were predictors of severe aGvHD (grade III or IV). Multivariate analysis showed that CTLp group (RR = 3.4, P = 0.015) and CMV status (RR = 3.9, P = 0.008) were predictors of leukemia-free survival. Further investigation showed an interaction between the two, such that CMV seropositive recipients in the high frequency group had a relative risk of 9.4 (P = 0.0001) of treatment failure (death or relapse) when compared with other combinations. We conclude that with our present GvHD prophylaxis regimen, CTLp frequency analysis predicts post-BMT outcome and is a valuable aid in donor selection.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0041-1337
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
59
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1302-8
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:7762066-Adolescent,
pubmed-meshheading:7762066-Adult,
pubmed-meshheading:7762066-Analysis of Variance,
pubmed-meshheading:7762066-Bone Marrow Transplantation,
pubmed-meshheading:7762066-Female,
pubmed-meshheading:7762066-Graft vs Host Disease,
pubmed-meshheading:7762066-Histocompatibility Testing,
pubmed-meshheading:7762066-Humans,
pubmed-meshheading:7762066-Leukemia, Myelogenous, Chronic, BCR-ABL Positive,
pubmed-meshheading:7762066-Male,
pubmed-meshheading:7762066-Middle Aged,
pubmed-meshheading:7762066-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:7762066-Tissue Donors
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pubmed:year |
1995
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pubmed:articleTitle |
Cytotoxic T lymphocyte precursor frequency analyses in bone marrow transplantation with volunteer unrelated donors. Value in donor selection.
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pubmed:affiliation |
LRF Centre for Adult Leukaemia, Royal Postgraduate Medical School, London, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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