Synovial mast cell responses during clinical improvement in early rheumatoid arthritis

被引:67
作者
Gotis-Graham, I
Smith, MD
Parker, A
McNeil, HP [1 ]
机构
[1] Univ New S Wales, Sch Pathol, Inflammat Res Unit, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Sch Med, Inflammat Res Unit, Sydney, NSW 2052, Australia
[3] Prince Wales Hosp, Dept Rheumatol, Sydney, NSW, Australia
[4] Repatriat Gen Hosp, Rheumatol Res Unit, Adelaide, SA, Australia
关键词
D O I
10.1136/ard.57.11.664
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives-To determine the synovial mast cell response in early rheumatoid arthritis (RA) during clinical improvement, and to examine for relations with clinical and histological parameters of disease activity. Methods-Twenty two synovial samples were obtained from six patients with RA using needle arthroscopy. The mean disease duration at baseline was eight months, and two to three further samples were obtained over a mean follow up period of 15 months during which treatment initiated clinical improvement occurred. Sections were immunostained to detect MCT and MCTC mast cells and correlations were sought between clinical and histological data. Results-The overall mean synovial mast cell density was 40.3 cells/mm(2), with regional densities of 60.6 and 34.2 mast cells/mm2 in the superficial and deeper synovial layers respectively. The MCT subset predominated, outnumbering MCTC by 3:1. There was a significant correlation between the histological inflammation index and the MCT density, (r = 0.4, p < 0.05) but not the MCTC subset. The regional distribution and predominant subset of mast cells varied in individual patient's synovia over time, with a trend towards restriction of the mast cell response to the superficial synovium during clinical improvement. Conclusions-The mast cell response in early RA is characterised by substantial expansion of predominantly MCT mast cells that correlates with histological indices of inflammation. During clinical improvement, this expansion tended to become more superficial. Taken together with previous studies of long duration RA, which implicate MCTC cells in synovial damage and disease progression, these results suggest that MCT and MCTC mast cells may possess distinct functions in the spectrum of inflammatory events occurring during RA.
引用
收藏
页码:664 / 671
页数:8
相关论文
共 42 条
[1]  
Algermissen B, 1994, Exp Dermatol, V3, P290, DOI 10.1111/j.1600-0625.1994.tb00291.x
[2]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[3]  
Baghestanian M, 1996, LEUKEMIA, V10, P159
[4]   CONJUGATED AVIDIN IDENTIFIES CUTANEOUS RODENT AND HUMAN MAST-CELLS [J].
BERGSTRESSER, PR ;
TIGELAAR, RE ;
THARP, MD .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1984, 83 (03) :214-218
[5]  
BRADDING P, 1995, J IMMUNOL, V155, P297
[6]   The presence of membrane-bound stem cell factor on highly immature nonmetachromatic mast cells in the peripheral blood of a patient with aggressive systemic mastocytosis [J].
Castells, MC ;
Friend, DS ;
Bunnell, CA ;
Hu, XZ ;
Kraus, M ;
Osteen, RT ;
Austen, KF .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1996, 98 (04) :831-840
[7]   Human synovial mast cells .1. Ultrastructural in situ and in vitro immunologic characterization [J].
dePaulis, A ;
Marino, I ;
Ciccarelli, A ;
deCrescenzo, G ;
Concardi, M ;
Verga, L ;
Arbustini, E ;
Marone, G .
ARTHRITIS AND RHEUMATISM, 1996, 39 (07) :1222-1233
[8]   RAT PERITONEAL MAST-CELLS PRESENT ANTIGEN TO A PPD-SPECIFIC T-CELL LINE [J].
FOX, CC ;
JEWELL, SD ;
WHITACRE, CC .
CELLULAR IMMUNOLOGY, 1994, 158 (01) :253-264
[9]  
FRANDJI P, 1993, J IMMUNOL, V151, P6318
[10]   Mast cells that reside at different locations in the jejunum of mice infected with Trichinella spiralis exhibit sequential changes in their granule ultrastructure and chymase phenotype [J].
Friend, DS ;
Ghildyal, N ;
Austen, KF ;
Gurish, MF ;
Matsumoto, R ;
Stevens, RL .
JOURNAL OF CELL BIOLOGY, 1996, 135 (01) :279-290