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Intravenous immunoglobulin modulates lymphocyte CD54 and monocyte FcγRII expression in patients with chronic inflammatory neuropathies
被引:35
作者:
Créange, A
Gregson, NA
Hughes, RAC
机构:
[1] Hop Henri Mondor, Serv Neurol, AP HP, F-94010 Creteil, France
[2] Univ Paris 12, F-94010 Creteil, France
[3] Guys Hosp, Guys Kings & St Thomas Sch Med, Dept Neuroimmunol, London SE1 1UL, England
关键词:
intravenous immunoglobulin;
integrins;
inflammatory neuropathy;
D O I:
10.1016/S0165-5728(02)00430-7
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
We studied the expression of different lymphocyte and monocyte cellular determinants involved in leukodiapedesis and antigen presentation in 10 patients with chronic inflammatory demyeclinating polyradiculoneuropathy (CIDP) and multifocal motor neuropathy (MMN) with persistent conduction blocks before intravenous immunoglobulin (IVIg), immediately after infusion of IVIg and I week after infusion. We observed a decrease of T lymphocytes expressing ICAM-1 (CD54) immediately after infusion in 8 out of 10 patients (p<0.04) with a return to pretreatment values after I week. The monocytes showed an increase in CD14(+) cells and CD14(+) FcgammaRII inhibitory receptor positive cells, no change in the number of CD W FcgammaRIII activation receptor cells, and an increase in the FcgammaRII/FcgammaRIII ratio on monocytes I week after IVIg. Thus, the mechanism of action of IVIg in both CIDP and MMN may involve inhibition of T cell transmigration and modulation of antigen presentation capacities through FcgammaR expression. (C) 2002 Elsevier Science B.V. All rights reserved.
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页码:91 / 95
页数:5
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