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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2006-2-7
pubmed:abstractText
We investigated the clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria (PNH)-type blood cells in patients with acquired aplastic anemia (AA). We quantified CD55-CD59- granulocytes and red blood cells (RBCs) in peripheral blood from 122 patients with recently diagnosed AA and correlated numbers of PNH-type cells and responses to immunosuppressive therapy (IST). Flow cytometry detected 0.005% to 23.1% of GPI-AP- cells in 68% of patients with AA. Sixty-eight of 83 (91%) patients with an increased proportion of PNH-type cells (PNH+) responded to antithymocyte globulin (ATG) + cyclosporin (CsA) therapy, whereas 18 of 39 (48%) without such an increase (PNH-) responded. Failure-free survival rates were significantly higher (64%) among patients with PNH+ than patients with PNH- (12%) at 5 years, although overall survival rates were comparable between the groups. Numbers of PNH-type and normal-type cells increased in parallel among most patients with PNH+ who responded to IST, suggesting that these cells are equally sensitive to immune attack. These results indicate that a minor population of PNH-type cells represents a reliable marker of a positive IST response and a favorable prognosis among patients with AA. Furthermore, immune attack against hematopoietic stem cells that allows PNH clonal expansion might occur only at the onset of AA.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0006-4971
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
107
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1308-14
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:16179371-Adolescent, pubmed-meshheading:16179371-Adult, pubmed-meshheading:16179371-Aged, pubmed-meshheading:16179371-Aged, 80 and over, pubmed-meshheading:16179371-Anemia, Aplastic, pubmed-meshheading:16179371-Antigens, CD, pubmed-meshheading:16179371-Antigens, CD55, pubmed-meshheading:16179371-Antigens, CD59, pubmed-meshheading:16179371-Antilymphocyte Serum, pubmed-meshheading:16179371-Chromosome Aberrations, pubmed-meshheading:16179371-Cyclosporine, pubmed-meshheading:16179371-Female, pubmed-meshheading:16179371-Flow Cytometry, pubmed-meshheading:16179371-Granulocytes, pubmed-meshheading:16179371-Humans, pubmed-meshheading:16179371-Immunosuppressive Agents, pubmed-meshheading:16179371-Leukocyte Count, pubmed-meshheading:16179371-Male, pubmed-meshheading:16179371-Middle Aged, pubmed-meshheading:16179371-Predictive Value of Tests, pubmed-meshheading:16179371-Survival Analysis
pubmed:year
2006
pubmed:articleTitle
Minor population of CD55-CD59- blood cells predicts response to immunosuppressive therapy and prognosis in patients with aplastic anemia.
pubmed:affiliation
Cellular Transplantation Biology, Division of Cancer Medicine, Kanazawa University Graduate School of Medical Science, 13-1 Takaramachi, Kanazawa, Ishikawa 920-8641, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't