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Cellular basis of ectopic germinal center formation and autoantibody production in the target organ of patients with Sjögren's syndrome
Abstract
Objective: To investigate functional properties of the germinal center (GC)–like structures observed in salivary glands of patients with Sjögren's syndrome (SS) and to determine the frequency with which such structures develop. Methods: Hematoxylin and eosin–stained sections from 165 minor salivary gland biopsy samples were screened for GC‐like structures. Expression of markers for GCs (CD3, CD20, Ki‐67, CD35, CD31), adhesion molecules (intercellular adhesion molecule 1, lymphocyte function–associated antigen 1, vascular cell adhesion molecule 1, very late activation antigen 4), chemokines (CXCL13, CCL21, CXCL12), and production of autoantibodies (anti‐Ro/SSA and anti‐La/SSB) was investigated by immunohistochemistry. Apoptosis was investigated by TUNEL staining. Results: GC‐like structures were observed in 28 of 165 patients (17%). When GCs were defined as T and B cell aggregates with proliferating cells with a network of follicular dendritic cells and activated endothelial cells, such microenvironments were found in all patients in whom structures with GC‐like morphology were observed. The defined microenvironments were not found in patients without apparent GC‐like structures. The GCs formed within the target tissue showed functional features with production of autoantibodies (anti‐Ro/SSA and anti‐La/SSB) and apoptotic events (by TUNEL staining), and the local production of anti‐Ro/SSA and anti‐La/SSB autoantibodies was significantly increased (P = 0.04) in patients with GC development. Conclusion: Lymphoid neogenesis and functional ectopic GC formation take place in salivary glands of a subset of patients with SS. Our data suggest that the ectopic secondary lymphoid follicles contain all elements needed for driving the autoimmune response. Our findings underscore a key role for the target organ in recruitment of inflammatory cells and propagation of the disease process.
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Cited by
Serafini, B., Rosicarelli, B., Magliozzi, R., Stigliano, E., & Aloisi, F. (2004) · Brain Pathology · doi:10.1111/j.1750-3639.2004.tb00049.x · Cited by 1,208
Ectopic lymphoid-like structures in infection, cancer and autoimmunity
Pitzalis, C., Jones, G. W., Bombardieri, M., & Jones, S. A. (2014) · Nature Reviews Immunology · doi:10.1038/nri3700 · Cited by 698
Immunopathogenic mechanisms of systemic autoimmune disease
Wahren-Herlenius, M., & Dörner, T. (2013) · The Lancet · doi:10.1016/s0140-6736(13)60954-x · Cited by 593
Self-citationHumby, F., Bombardieri, M., Manzo, A., Kelly, S., Blades, M. C., Kirkham, B., Spencer, J., & Pitzalis, C. (2009) · PLoS Medicine · doi:10.1371/journal.pmed.0060001 · Cited by 537
Autoantibodies in systemic autoimmune diseases: specificity and pathogenicity
Suurmond, J., & Diamond, B. (2015) · Journal of Clinical Investigation · doi:10.1172/jci78084 · Cited by 337
Metadata
- Authors
- Salomonsson, S., Jonsson, M. V., Skarstein, K., Brokstad, K. A., Hjelmström, P., Wahren‐Herlenius, M., & Jonsson, R.
- Venue
- Arthritis & Rheumatism
- Publisher
- Wiley
- Published
- 2003-11
- Volume
- 48
- Issue
- 11
- Pages
- 3187-3201
- ISSN
- 0004-3591 (ISSN-L)
- 1529-0131
- OpenAlex
- W2055671309
- Cited by
- 472
- References
- 0
- FWCI
- 8.50
- Type
- journal article
- Language
- en
- Open access
- closed
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- Salomonsson, S., Jonsson, M. V., Skarstein, K., Brokstad, K. A., Hjelmström, P., Wahren‐Herlenius, M., & Jonsson, R. (2003). Cellular basis of ectopic germinal center formation and autoantibody production in the target organ of patients with Sjögren's syndrome. Arthritis & Rheumatism. https://doi.org/10.1002/art.11311
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