Adjunctive high-dose intravenous immunoglobulin treatment for resistant atopic dermatitis: Efficacy and effects on intracellular cytokine levels and CD4 counts
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Jolles, S
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机构:Natl Inst Med Res, Div Infect & Immun, London NW7 1AA, England
Jolles, S
Sewell, C
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机构:Natl Inst Med Res, Div Infect & Immun, London NW7 1AA, England
Sewell, C
Webster, D
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机构:Natl Inst Med Res, Div Infect & Immun, London NW7 1AA, England
Webster, D
Ryan, A
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机构:Natl Inst Med Res, Div Infect & Immun, London NW7 1AA, England
Ryan, A
Heelan, B
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机构:Natl Inst Med Res, Div Infect & Immun, London NW7 1AA, England
Heelan, B
Waite, A
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机构:Natl Inst Med Res, Div Infect & Immun, London NW7 1AA, England
Waite, A
Rustin, M
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机构:Natl Inst Med Res, Div Infect & Immun, London NW7 1AA, England
Rustin, M
机构:
[1] Natl Inst Med Res, Div Infect & Immun, London NW7 1AA, England
[2] Royal Free Hosp, Dept Immunol, London NW3 2QG, England
[3] Royal Free Hosp, Dept Dermatol, London NW3 2QG, England
Although atopic dermatitis generally responds to topical therapy, small numbers of patients have severe resistant disease despite second-line therapies. High-dose intravenous immunoglobulin has been suggested to be of benefit in a small number of reports. We have conducted an open, single-centre study of adjunctive high-dose intravenous immunoglobulin (Flebogamma(R) 5%). Six patients received treatment at 2 g kg(-1) month(-1) for 6 cycles, with a 3-month follow-up period. Skin scores, lymphocyte phenotypes and intracellular cytokine analysis were performed. Four of six patients had major improvements in skin scores and the overall reduction was significant (p=0.035). CD4+ T-cell numbers fell following high-dose intravenous immunoglobulin infusions, recovering by the next cycle. T-cell CD69 expression decreased to 60% of baseline values. Reductions in the proinflammatory cytokines IFN-gamma and TNF-alpha were non-significant. Adjunctive high-dose intravenous immunoglobulin may be a useful therapeutic approach in adults with severe treatment-resistant atopic dermatitis, but it will require further assessment in randomized controlled trials to establish this.