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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0024109,
umls-concept:C0030705,
umls-concept:C0035820,
umls-concept:C0039194,
umls-concept:C0077503,
umls-concept:C0085236,
umls-concept:C0185117,
umls-concept:C0205276,
umls-concept:C0301872,
umls-concept:C0596901,
umls-concept:C0851285,
umls-concept:C1456820,
umls-concept:C1705535,
umls-concept:C2911684
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pubmed:issue |
6
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pubmed:dateCreated |
1995-4-6
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pubmed:abstractText |
High amounts of TNF-alpha are released by alveolar macrophages (AMs) in the lungs of patients with HIV-1 infection. To investigate the role of this cytokine in the local immune response, we studied the expression of surface receptors for TNF-alpha (TNF-Rs) and the presence of the transmembrane form of TNF-alpha (mTNF-alpha) on bronchoalveolar lavage (BAL) cells recovered from 14 patients with HIV-1 infection. The role of TNF-alpha both in the events leading to the T cell alveolitis and as a mediator of cytotoxicity was also evaluated. TNF-R expression was determined by flow cytometry on BAL CD8 lymphocytes and AMs (i.e., the cells that account for the alveolitis in HIV-1 infection). We found that CD8 cells express the 75-kDa (CD120a) but not the 55-kDa (CD120a) TNF-Rs, whereas AMs were devoid of TNF-R expression. More than 90% of BAL T cells efficiently bound TNF-alpha; when T cells were tested for their proliferative capacity, an up-regulation of the IL-2-mediated proliferation by TNF-alpha was observed, suggesting that this cytokine may drive the in situ proliferation of CD120b+ T cells. As shown by flow cytometry analysis and immunoprecipitation with anti-TNF-alpha Ab, mTNF-alpha expression was observed on AMs but not on alveolar T cells. Fixed AMs showed high levels of killing against TNF-sensitive targets. Taken together, our data demonstrate the selective expression of TNF-Rs and mTNF-alpha on cells accumulating within the alveolar spaces of patients with HIV-1 infection, pointing to the compound role of TNF-alpha in the local immune responses.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
154
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2928-38
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7876559-Adult,
pubmed-meshheading:7876559-Cells, Cultured,
pubmed-meshheading:7876559-Cytotoxicity, Immunologic,
pubmed-meshheading:7876559-Female,
pubmed-meshheading:7876559-Flow Cytometry,
pubmed-meshheading:7876559-HIV Infections,
pubmed-meshheading:7876559-HIV-1,
pubmed-meshheading:7876559-Humans,
pubmed-meshheading:7876559-Lung,
pubmed-meshheading:7876559-Lymphocyte Activation,
pubmed-meshheading:7876559-Macrophages, Alveolar,
pubmed-meshheading:7876559-Male,
pubmed-meshheading:7876559-Precipitin Tests,
pubmed-meshheading:7876559-Receptors, Tumor Necrosis Factor,
pubmed-meshheading:7876559-T-Lymphocytes,
pubmed-meshheading:7876559-Tumor Necrosis Factor-alpha
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pubmed:year |
1995
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pubmed:articleTitle |
Expression of TNF receptors by T cells and membrane TNF-alpha by alveolar macrophages suggests a role for TNF-alpha in the regulation of the local immune responses in the lung of HIV-1-infected patients.
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pubmed:affiliation |
Padua University School of Medicine, Department of Clinical Medicine, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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