Peripheral blood mononuclear cells of multiple sclerosis (MS) patients were stimulated with myelin basic protein (MBP) together with anti-CD28 monoclonal antibody and staphylococcal enterotoxin B to optimize cytokine production by antigen-specific cells. Type 1 IL-2, IL-12, IFNgamma) and pro-inflammatory (TNFalpha, IL-1beta, IL-6) cytokines were augmented in CD4 +, CD8 +, and CD14 + cells of acute MS patients and of patients undergoing disease reactivation. These cytokines were reduced in IFNbeta-treated and in stable MS patients; type 2 cytokines (IL-4, IL-10) were increased in these patients. Similar immune profiles are seen in MS patient in whom remission is naturally or pharmacologically (IFNbeta) achieved. Cytokine alterations are particularly evident in CD14 + cells, underlying their critical role in the modulation of the immune response. (C) 2001 Elsevier Science B.V. All rights reserved.
机构:
Vanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USAVanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USA
Bright, JJ
Xin, ZC
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Vanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USAVanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USA
Xin, ZC
Sriram, S
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Vanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USAVanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USA
机构:
Vanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USAVanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USA
Bright, JJ
Xin, ZC
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Vanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USAVanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USA
Xin, ZC
Sriram, S
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Vanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USAVanderbilt Univ, Med Ctr, Multiple Sclerosis Res Lab, Nashville, TN 37212 USA