Lymphoid organisation in labial salivary gland biopsies is a possible predictor for the development of malignant lymphoma in primary Sjogren's syndrome

被引:338
作者
Theander, Elke [2 ]
Vasaitis, Lilian [3 ]
Baecklund, Eva [3 ]
Nordmark, Gunnel [3 ]
Warfvinge, Gunnar [4 ]
Liedholm, Rolf [5 ]
Brokstad, Karl [1 ]
Jonsson, Roland [1 ,6 ]
Jonsson, Malin V. [1 ,7 ]
机构
[1] Univ Bergen, Broegelmann Res Lab, Gade Inst, N-5021 Bergen, Norway
[2] Lund Univ, Dept Rheumatol, Skane Univ Hosp Malmo, Lund, Sweden
[3] Uppsala Univ, Dept Med Sci, Rheumatol Sect, Uppsala, Sweden
[4] Malmo Univ, Dept Oral Pathol, Malmo, Sweden
[5] Skane Univ Hosp Malmo, Dept Oral & Maxillofacial Surg, Malmo, Sweden
[6] Haukeland Hosp, Dept Rheumatol, N-5021 Bergen, Norway
[7] Univ Bergen, Inst Med, Rheumatol Sect, N-5021 Bergen, Norway
关键词
AUTOANTIBODY PRODUCTION; TARGET ORGAN; DISEASE; RISK; MORTALITY; CLASSIFICATION; MECHANISMS; AUTOIMMUNE; MEMORY; COHORT;
D O I
10.1136/ard.2010.144782
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective The development of non-Hodgkin's lymphoma (NHL) confers a high risk of mortality in primary Sjogren's syndrome (pSS) patients, but the sensitivity and specificity of proposed lymphoma predictors are insufficient for practical use. The performance of lymphoid organisation in the form of germinal centre (GC)-like lesions was evaluated in labial salivary gland biopsies taken at pSS diagnosis as a potential lymphoma-predicting biomarker. Methods Labial salivary gland tissue biopsies available from two Swedish pSS research cohorts (n = 175) were re-evaluated by light microscopy in a blind study in order to identify GC-like structures as a sign of ectopic lymphoid tissue formation and organisation. A linkage study was performed with the Swedish Cancer Registry for lymphoma identification. The risk of developing NHL in GC-positive patients in comparison with GC-negative patients was evaluated using Kaplan-Meier statistics and log-rank test. Associations between GC-like structures and clinical and/or laboratory disease markers were also determined using. 2 or Fisher's exact tests. Results At diagnosis, 25% of pSS patients had GC-like structures in their salivary glands. Seven of the 175 patients studied (14% GC+ and 0.8% GC-) developed NHL during 1855 patient-years at risk, with a median onset of 7 years following the initial diagnostic salivary gland biopsy. Six of the seven patients had GC-like structures at diagnosis; the remaining patient was GC negative at the time of diagnosis (p=0.001). Conclusions The detection of GC-like structures by light microscopy in pSS diagnostic salivary biopsies is proposed as a highly predictive and easy-to-obtain marker for NHL development. This allows for risk stratification of patients and the possibility to initiate preventive B-cell-directed therapy.
引用
收藏
页码:1363 / 1368
页数:6
相关论文
共 31 条
[1]
Abnormal B cell differentiation in primary Sjogren's syndrome results in a depressed percentage of circulating memory B cells and elevated levels of soluble CD27 that correlate with serum IgG concentration [J].
Bohnhorst, JO ;
Bjorgan, MB ;
Thoen, JE ;
Jonsson, R ;
Natvig, JB ;
Thompson, KM .
CLINICAL IMMUNOLOGY, 2002, 103 (01) :79-88
[2]
LABIAL SALIVARY GLAND BIOPSY IN SJOGRENS DISEASE [J].
CHISHOLM, DM ;
MASON, DK .
JOURNAL OF CLINICAL PATHOLOGY, 1968, 21 (05) :656-&
[3]
Extrasalivary lymphoma development in Sjogren's syndrome - Clonal evolution from parotid gland lymphoproliferation and role of local triggering [J].
Gasparotto, D ;
De Vita, S ;
De Re, V ;
Marzotto, A ;
De Marchi, G ;
Scott, CA ;
Gloghini, A ;
Ferraccioli, G ;
Boiocchi, M .
ARTHRITIS AND RHEUMATISM, 2003, 48 (11) :3181-3186
[4]
Activation of IFN pathways and plasmacytoid dendritic cell recruitment in target organs of primary Sjogren's syndrome [J].
Gottenberg, JE ;
Cagnard, N ;
Lucchesi, C ;
Letourneur, F ;
Mistou, S ;
Lazure, T ;
Jacques, S ;
Ba, N ;
Ittah, M ;
Lepajolec, C ;
Labetoulle, M ;
Ardizzone, M ;
Sibilia, J ;
Fournier, C ;
Chiocchia, G ;
Mariette, X .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (08) :2770-2775
[5]
Immunopathogenesis of primary Sjogren's syndrome:: implications for disease management and therapy [J].
Hansen, A ;
Lipsky, PE ;
Dörner, T .
CURRENT OPINION IN RHEUMATOLOGY, 2005, 17 (05) :558-565
[6]
Abnormalities in peripheral B cell memory of patients with primary Sjogren's Syndrome [J].
Hansen, A ;
Gosemann, M ;
Pruss, A ;
Reiter, K ;
Ruzickova, S ;
Lipsky, PE ;
Dörner, T .
ARTHRITIS AND RHEUMATISM, 2004, 50 (06) :1897-1908
[7]
Aspects of B-Cell Non-Hodgkin's Lymphoma Development: A Transition from Immune-Reactivity to Malignancy [J].
Illes, A. ;
Varoczy, L. ;
Papp, G. ;
Wilson, P. C. ;
Alex, P. ;
Jonsson, R. ;
Kovacs, T. ;
Konttinen, Y. T. ;
Zeher, M. ;
Nakken, B. ;
Szodoray, P. .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2009, 69 (05) :387-400
[8]
Long-term risk of mortality and lymphoproliferative disease and predictive classification of primary Sjogren's syndrome [J].
Ioannidis, JPA ;
Vassiliou, VA ;
Moutsopoulos, HM .
ARTHRITIS AND RHEUMATISM, 2002, 46 (03) :741-747
[9]
Jonsson MV, 2007, J RHEUMATOL, V34, P2044
[10]
Association between circulating levels of the novel TNF family members APRIL and BAFF and lymphoid organization in primary Sjogren's syndrome [J].
Jonsson, MV ;
Szodoray, P ;
Jellestad, S ;
Jonsson, R ;
Skarstein, K .
JOURNAL OF CLINICAL IMMUNOLOGY, 2005, 25 (03) :189-201