Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1994-7-8
pubmed:abstractText
The immunodeficiency that occurs after human bone marrow transplantation (BMT) leaves BMT recipients susceptible to fatal infections. Although cytokines are critical for coordinating immune responses and immune reconstitution after BMT, there are still gaps in our knowledge about the expression of mRNA for cytokines in peripheral blood mononuclear cells (PBMC) after BMT. Therefore, we systematically studied cytokine gene expression by PBMC from 11 allogeneic and four autologous BMT recipients from 111 to 837 days after BMT and compared the results with PBMC from seven normal controls tested in parallel. PBMC were examined for mRNA expression for IL-2r alpha, IL-2, IL-3, IL-4, IL-6, and IL-7 using reverse transcription polymerase chain reaction (RT/PCR). PBMC from 11 allogeneic recipients constitutively expressed mRNA for IL-2r alpha in 2 of 11 and IL-2 in 1 of 9 samples tested whereas the same PBMC constitutively expressed mRNA for IL-3 in 8 of 11, IL-4 in 3 of 7, IL-6 in 6 of 7 and IL-7 in 3 of 6 samples tested. After PHA/PMA stimulation, PBMC from the same recipients frequently expressed mRNA for IL-2r alpha in 9 of 11, IL-2 in 8 of 9, IL-4 in 3 of 7 and IL-6 in 7 of 7. PBMC from four autologous recipients (two short-term and two long-term) frequently constitutively expressed mRNA for IL-2r alpha (3 of 4) IL-2 (3 of 4), and IL-3 (4 of 4). Stimulation of PBMC from the autologous recipients did not alter cytokine expression.(ABSTRACT TRUNCATED AT 250 WORDS)
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0268-3369
pubmed:author
pubmed:issnType
Print
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
187-95
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:8205088-Anemia, Aplastic, pubmed-meshheading:8205088-Base Sequence, pubmed-meshheading:8205088-Bone Marrow Transplantation, pubmed-meshheading:8205088-Cytokines, pubmed-meshheading:8205088-Humans, pubmed-meshheading:8205088-Interleukin-2, pubmed-meshheading:8205088-Interleukin-3, pubmed-meshheading:8205088-Interleukin-4, pubmed-meshheading:8205088-Interleukin-6, pubmed-meshheading:8205088-Interleukin-7, pubmed-meshheading:8205088-Leukemia, Myelogenous, Chronic, BCR-ABL Positive, pubmed-meshheading:8205088-Leukocytes, Mononuclear, pubmed-meshheading:8205088-Mitogens, pubmed-meshheading:8205088-Molecular Sequence Data, pubmed-meshheading:8205088-Myelodysplastic Syndromes, pubmed-meshheading:8205088-Phenotype, pubmed-meshheading:8205088-Polymerase Chain Reaction, pubmed-meshheading:8205088-RNA, Messenger, pubmed-meshheading:8205088-Transplantation, Autologous, pubmed-meshheading:8205088-Transplantation, Homologous
pubmed:year
1994
pubmed:articleTitle
Constitutive and mitogen-stimulated cytokine mRNA expression by peripheral blood mononuclear cells from most autologous and allogeneic bone marrow transplant recipients is intact.
pubmed:affiliation
Department of Medicine, Wayne State University, Detroit.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't