Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0006837,
umls-concept:C0021760,
umls-concept:C0027950,
umls-concept:C0033268,
umls-concept:C0065678,
umls-concept:C0086418,
umls-concept:C0333516,
umls-concept:C0681850,
umls-concept:C1264633,
umls-concept:C1456820,
umls-concept:C1550501,
umls-concept:C1706203,
umls-concept:C1948023,
umls-concept:C2349001,
umls-concept:C2349975,
umls-concept:C2697811
|
pubmed:issue |
3
|
pubmed:dateCreated |
1997-4-4
|
pubmed:abstractText |
IL-1beta, IL-6, IL-8 and TNF-alpha production by PMNL from 21 HIV-infected (HIV+), including 11 full-blown AIDS, and 20 HIV-uninfected (HIV-) subjects (matched for age and sex to HIV+ ones) was studied by reverse transcriptase-polymerase chain reaction (RT-PCR) and ELISA. PMNL from both categories of subjects were strongly stimulated in their actual cytokine production by a mannoprotein fraction (MP-F2) of Candida albicans, as well as by the bacterial lipopolysaccharide (LPS). These stimulatory effects were apparently due to increased cytokine gene expression and were substantially reversed by the physiological inhibitor IL-10. However, PMNL from HIV+ subjects showed increased IL-6 and TNF-alpha gene expression and produced more IL-6 and TNF-alpha than PMNL from HIV- controls, under similar stimulation conditions. This difference could not be attributed to a given stage of HIV infection, any associated medication, or to a generalized increase of gene expression, as quantitatively similar beta-actin and IL-1beta transcripts were detected. Moreover, no significant difference in IL-8 production by the PMNL from HIV+ and HIV- subjects was observed. Our studies suggest that PMNL from HIV+ subjects might add to other cellular sources of IL-6 and TNF-alpha (e.g. monocytes-macrophages) in contributing to the cytokine-dysregulated pattern typical of the HIV+ patient.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-10,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-6,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-8,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/mannoproteins
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0009-9104
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
107
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
451-7
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9067516-Adult,
pubmed-meshheading:9067516-Candida albicans,
pubmed-meshheading:9067516-Cells, Cultured,
pubmed-meshheading:9067516-Female,
pubmed-meshheading:9067516-Fungal Proteins,
pubmed-meshheading:9067516-HIV Infections,
pubmed-meshheading:9067516-Humans,
pubmed-meshheading:9067516-Interleukin-1,
pubmed-meshheading:9067516-Interleukin-10,
pubmed-meshheading:9067516-Interleukin-6,
pubmed-meshheading:9067516-Interleukin-8,
pubmed-meshheading:9067516-Male,
pubmed-meshheading:9067516-Membrane Glycoproteins,
pubmed-meshheading:9067516-Middle Aged,
pubmed-meshheading:9067516-Neutrophil Activation,
pubmed-meshheading:9067516-Neutrophils,
pubmed-meshheading:9067516-Peptide Fragments,
pubmed-meshheading:9067516-Tumor Necrosis Factor-alpha
|
pubmed:year |
1997
|
pubmed:articleTitle |
Responsiveness of human polymorphonuclear cells (PMNL) to stimulation by a mannoprotein fraction (MP-F2) of Candida albicans; enhanced production of IL-6 and tumour necrosis factor-alpha (TNF-alpha) by MP-F2-stimulated PMNL from HIV-infected subjects.
|
pubmed:affiliation |
Department of Bacteriology and Medical Mycology, Istituto Superiore di Sanità, University of Rome La Sapienza, Italy.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|