Serum and cerebrospinal fluid soluble Fas levels in clinical subgroups of multiple sclerosis

被引:13
作者
Boylan, MT
Crockard, AD
McDonnell, GV
McMillan, SA
Hawkins, SA
机构
[1] Royal Grp Hosp Trust, Reg Immunol Serv, Belfast BT12 6BA, Antrim, North Ireland
[2] Queens Univ Belfast, Royal Grp Hosp Trust, Dept Microbiol & Immunobiol, Belfast BT12 6BA, Antrim, North Ireland
[3] Queens Univ Belfast, Royal Grp Hosp Trust, Dept Med, Belfast BT12 6BA, Antrim, North Ireland
关键词
apoptosis; interferon-beta; multiple sclerosis; soluble Fas;
D O I
10.1016/S0165-2478(01)00244-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Elevated sFas levels have been described in Multiple sclerosis (MS) patients with active disease. The aim of this study was to assess the diagnostic potential of serum and cerebrospinal fluid (CSF) sFas measurements in differentiating clinically defined MS patient subgroups. Levels of sFas and sFas indices were determined in patients with stable relapsing-remitting MS (RRMS), active RRMS, primary progressive MS (PPMS), secondary progressive MS (SPMS) and patients with inflammatory (IND) and noninflammatory neurological diseases (NIND). Serum sFas modulation over 32 weeks IFN-beta la therapy was also investigated. Serum and CSF sFas levels and sFas indices were elevated in MS compared to NIND and IND patients. Within the MS group, serum and CSF sFas levels were highest in PPMS, with active RRMS patients demonstrating the highest sFas indices. This may reflect an ongoing disease process which is occurring acutely (active disease) or incessantly (progressive disease). IFN-beta la induced a transient increase in circulating sFas following initiation of therapy. Whilst evidence was provided for variable sFas expression in clinical subgroups of MS, there was insufficient definition between the respective groups to advocate sFas measurements as a diagnostic marker of clinical subgroups of MS. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:183 / 187
页数:5
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