Extended report
Analysis of the cell infiltrate and expression of matrix
metalloproteinases and granzyme B in paired synovial biopsy specimens
from the cartilage-pannus junction in patients with RA
T J M Smeetsa, M C Kraana, S Galjaardb, P P Youssefc, M D Smithd, P P Taka
a Division of
Clinical Immunology and Rheumatology, Academic Medical Centre,
Amsterdam, The Netherlands, b Department of Rheumatology,
Leiden University Medical Centre, The Netherlands, c Department of Pathology, University of New South
Wales, Sydney, Australia, d Rheumatology
Research Unit, Repatriation General Hospital, Daw Park, SA, Australia
Correspondence to: T J M Smeets, Division of Clinical Immunology and Rheumatology, Department of Medicine, Academic Medical Centre, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands T.J.Smeets{at}amc.uva.nl
Accepted for publication 17 November
2000
OBJECTIVES
Examination
of synovial tissue (ST) obtained at surgery because of end stage
destructive rheumatoid arthritis (RA) showed that macrophages and
fibroblasts are the major cell types at the cartilage-pannus junction
(CPJ). This study aimed at defining the cell infiltrate and mediators
of joint destruction in ST selected at arthroscopy from the CPJ in
patients with RA who did not require joint surgery.
METHODS
Paired
synovial biopsy specimens were obtained at arthroscopy from ST adjacent
to the CPJ and the suprapatellar pouch from the knee joints of 17 patients with RA. Immunohistological analysis was performed using
monoclonal antibodies to detect T cells, B cells, plasma cells,
macrophages, fibroblast-like synoviocytes, mast cells, and granzyme B+
cytotoxic cells as well as the expression of metalloproteinase (MMP)-1,
MMP-3, and MMP-13. The sections were evaluated by computer assisted
image analysis and semiquantitative analysis.
RESULTS
The cell
infiltrate comprised mainly T cells, macrophages, and plasma cells. The
ST was also infiltrated by the other cell types, but at lower numbers.
Expression of MMPs was abundant, especially MMP-3. The features of ST
at the CPJ were generally similar to those at the suprapatellar pouch.
CONCLUSIONS
The
synovium at the CPJ in patients with RA who did not require joint
surgery exhibits, in general, the same type of cell infiltrate and
expression of MMPs and granzymes as ST from the suprapatellar pouch.
The pathological changes that have been described at the CPJ in
patients with RA with end stage, destructive disease may well reflect
the transition to a process in which macrophages, fibroblast-like
synoviocytes, and other cell types become increasingly important.
© 2001 by Annals of the Rheumatic Diseases
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