The Relationship Between Synovial Lymphocyte Aggregates and the Clinical Response to Infliximab in Rheumatoid Arthritis A Prospective Study

被引:80
作者
Klaasen, Ruth [1 ]
Thurlings, Rogier M. [1 ]
Wijbrandts, Carla A. [1 ]
van Kuijk, Arno W. [1 ]
Baeten, Dominique [1 ]
Gerlag, Danielle M. [1 ]
Tak, Paul P. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Div Clin Immunol & Rheumatol, NL-1105 AZ Amsterdam, Netherlands
来源
ARTHRITIS AND RHEUMATISM | 2009年 / 60卷 / 11期
关键词
TUMOR-NECROSIS-FACTOR; FACTOR-ALPHA THERAPY; DISEASE-ACTIVITY; CELL INFILTRATE; PSORIATIC-ARTHRITIS; MONOCLONAL-ANTIBODY; TISSUE; VALIDATION; EXPRESSION; NEOGENESIS;
D O I
10.1002/art.24913
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective. Some patients with rheumatoid arthritis (RA) exhibit lymphocyte aggregates in the synovium. This study was undertaken to address whether the presence of lymphocyte aggregates before treatment could serve as a biomarker for the clinical response to tumor necrosis factor (TNF) blockade, and to confirm whether the aggregation of synovial lymphocytes is reversible after anti-TNF treatment. Methods. Synovial tissue biopsy samples were obtained from 97 patients with active RA before the initiation of infliximab treatment. Lymphocyte aggregates in the synovial tissue were counted and also graded for size. Logistic regression analysis was performed to identify whether the presence of lymphocyte aggregates could be a predictor of the clinical response at week 16. Furthermore, the effects of TNF blockade on lymphocyte aggregates were compared between patients with RA and patients with psoriatic arthritis (PsA). Results. Fifty-seven percent of RA synovial tissue samples contained lymphocyte aggregates, and 32% of the patients had large aggregates. Aggregates were found in 67% of clinical responders compared with 38% of nonresponders. The presence of aggregates at baseline was a highly significant predictor of the clinical response to anti-TNF treatment (R-2 = 0.10, P = 0.008). Positivity for lymphocyte aggregates increased the power to predict the clinical response (R-2 = 0.29), when analyzed in a prediction model that included baseline disease activity evaluated by the Disease Activity Score in 28 joints, anti-cyclic citrullinated peptide antibody positivity, and synovial TNF alpha expression. There was a reduction in lymphocyte aggregates after anti-TNF antibody therapy in both RA and PsA. Conclusion. RA patients with synovial lymphocyte aggregates have, on average, a better response to infliximab treatment than those with only diffuse leukocyte infiltration. Moreover, the aggregation of synovial lymphocytes is reversible after anti-TNF antibody treatment.
引用
收藏
页码:3217 / 3224
页数:8
相关论文
共 34 条
[1]
Clinical response to adalimumab: relationship to anti-adalimumab antibodies and serum adalimumab concentrations in rheumatoid arthritis [J].
Bartelds, Geertje M. ;
Wijbrandts, Carla A. ;
Nurmohamed, Michael T. ;
Stapel, Steven ;
Lems, Willem F. ;
Aarden, Lucien ;
Dijkmans, Ben A. C. ;
Tak, Paul Peter ;
Wolbink, Gerrit Jan .
ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 (07) :921-926
[2]
Clinical significance of synovial lymphoid neogenesis and its reversal after anti-tumour necrosis factor α therapy in rheumatoid arthritis [J].
Canete, J. D. ;
Celis, R. ;
Moll, C. ;
Izquierdo, E. ;
Marsal, S. ;
Sanmarti, R. ;
Palacin, A. ;
Lora, D. ;
de la Cruz, J. ;
Pablos, J. L. .
ANNALS OF THE RHEUMATIC DISEASES, 2009, 68 (05) :751-756
[3]
Ectopic lymphoid neogenesis in psoriatic arthritis [J].
Canete, Juan D. ;
Santiago, Begona ;
Cantaert, Tineke ;
Sanmarti, Raimon ;
Palacin, Antonio ;
Celis, Raquel ;
Graell, Eduard ;
Gil-Torregrosa, Beatriz ;
Baeten, Dominique ;
Pablos, Jose L. .
ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 (06) :720-726
[4]
B lymphocyte autoimmunity in rheumatoid synovitis is independent of ectopic lymphoid neogenesis [J].
Cantaert, Tineke ;
Kolln, Johanna ;
Timmer, Trieneke ;
Kraan, Tineke C. van der Pouw ;
Vandooren, Bernard ;
Thurlings, Rogier M. ;
Canete, Juan D. ;
Catrina, Anca I. ;
Out, Theo ;
Verweij, Cor L. ;
Zhang, Yiping ;
Tak, Paul P. ;
Baeten, Dominique .
JOURNAL OF IMMUNOLOGY, 2008, 181 (01) :785-794
[5]
RANDOMIZED DOUBLE-BLIND COMPARISON OF CHIMERIC MONOCLONAL-ANTIBODY TO TUMOR-NECROSIS-FACTOR-ALPHA (CA2) VERSUS PLACEBO IN RHEUMATOID-ARTHRITIS [J].
ELLIOTT, MJ ;
MAINI, RN ;
FELDMANN, M ;
KALDEN, JR ;
ANTONI, C ;
SMOLEN, JS ;
LEEB, B ;
BREEDVELD, FC ;
MACFARLANE, JD ;
BIJL, H ;
WOODY, JN .
LANCET, 1994, 344 (8930) :1105-1110
[6]
Fonseca JE, 2000, CLIN EXP RHEUMATOL, V18, P559
[7]
Fonseca JE, 2005, CLIN EXP RHEUMATOL, V23, P185
[8]
Ectopic Lymphoid Structures Support Ongoing Production of Class-Switched Autoantibodies in Rheumatoid Synovium [J].
Humby, Frances ;
Bombardieri, Michele ;
Manzo, Antonio ;
Kelly, Stephen ;
Blades, Mark C. ;
Kirkham, Bruce ;
Spencer, Jo ;
Pitzalis, Costantino .
PLOS MEDICINE, 2009, 6 (01) :59-75
[9]
Klimiuk PA, 1997, AM J PATHOL, V151, P1311
[10]
Comparison of synovial tissues from the knee joints and the small joints of rheumatoid arthritis patients - Implications for pathogenesis and evaluation of treatment [J].
Kraan, MC ;
Reece, RJ ;
Smeets, TJM ;
Veale, DJ ;
Emery, P ;
Tak, PP .
ARTHRITIS AND RHEUMATISM, 2002, 46 (08) :2034-2038