Source:http://linkedlifedata.com/resource/pubmed/id/12182469
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2002-8-16
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pubmed:abstractText |
Anti-CD25 mAb's are used for prophylaxis of rejection in allograft transplantation. These agents target the alpha-chain, part of the IL-2Ralphabetagamma complex. The beta- and gamma-chain are signaling components that are not specific for IL-2. The T-cell growth factors IL2, IL-7 and IL-15 utilize the gamma-chain and IL-2 and IL-15 share the beta-chain. We have studied the consequences of targeting the IL-2R alpha-chain with the anti-CD25 mAb basiliximab by measuring the IL-2R alphabetagamma expression levels and the IL-2, IL-7 and IL-15 driven proliferation. By flowcytometry and limiting dilution analysis, the IL-2R complex was analyzed in peripheral blood samples from renal allograft recipients (n = 29) who received basiliximab (20 mg IV bolus on day 0 and 4), cyclosporin and mycophenolate mofetil. In peripheral blood, after induction therapy with basiliximab, no CD25 positive T-cells were detectable for 61 days (median, range 25-93 days). When CD25 cells were covered with basiliximab, the percentage and the mean fluorescence intensity (MFI) of IL-2Rbeta positive T-cells significantly decreased, P = 0.02 and P = 0.013, respectively, whereas the expression level of the IL-2Rgamma was not affected. The inhibition of the expression of the IL-2R alpha- and beta-chain had significant consequences for the function of these cells. Both the IL-2- and the IL-15-dependent proliferation were inhibited, P = 0.007 and P = 0.01, respectively. The control, the IL-7 driven proliferation, was not influenced by basiliximab. In conclusion, therapy with anti-CD25 mAb's affect T-cell-dependent allogeneic immune responses, not only by blocking IL-2 signaling but also by impairing IL-15 signaling through downregulating the IL-2/IL-15 receptor beta-chain.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Immunosuppressive Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-15,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/basiliximab
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0966-3274
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
81-7
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:12182469-Antibodies, Monoclonal,
pubmed-meshheading:12182469-Flow Cytometry,
pubmed-meshheading:12182469-Humans,
pubmed-meshheading:12182469-Immunosuppressive Agents,
pubmed-meshheading:12182469-Interleukin-15,
pubmed-meshheading:12182469-Kidney Transplantation,
pubmed-meshheading:12182469-Lymphocyte Activation,
pubmed-meshheading:12182469-Receptors, Interleukin-2,
pubmed-meshheading:12182469-Recombinant Fusion Proteins,
pubmed-meshheading:12182469-T-Lymphocytes,
pubmed-meshheading:12182469-Transplantation, Homologous
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pubmed:year |
2002
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pubmed:articleTitle |
Inhibition of the IL-15 pathway in anti-CD25 mAb treated renal allograft recipients.
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pubmed:affiliation |
Department of Internal Medicine, University Hospital Rotterdam-Dijkzigt, The Netherlands. baan@inwl.azr.nl
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pubmed:publicationType |
Journal Article
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