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Chlamydophila psittaci-negative ocular adnexal marginal zone lymphomas express self polyreactive B-cell receptors.

Authors :
Zhu, D
Bhatt, S
Lu, X
Guo, F
Veelken, H
Hsu, D K
Liu, F-T
Alvarez Cubela, S
Kunkalla, K
Vega, F
Chapman-Fredricks, J R
Lossos, I S
Source :
Leukemia (08876924). Jul2015, Vol. 29 Issue 7, p1587-1599. 13p. 5 Color Photographs, 1 Chart, 3 Graphs.
Publication Year :
2015

Abstract

The pathogenesis of Chlamydophila psittaci-negative ocular adnexal extranodal marginal zone lymphomas (OAEMZLs) is poorly understood. OAEMZLs are monoclonal tumors expressing a biased repertoire of mutated surface immunoglobulins. Antigenic activation of the B-cell receptor (BCR) may have a role in the pathogenesis of these lymphomas. We have analyzed the reactivity of recombinant OAEMZL immunoglobulins. OAEMZL antibodies reacted with self-human antigens, as demonstrated by enzyme-linked immunosorbent assays, HEp-2 immunofluorescence and human protein microarrays. All the analyzed recombinant antibodies (rAbs) exhibited polyreactivity by comprehensive protein array antibody reactivity and some rAbs also demonstrated rheumatoid factor activity. The identity of several reactive antigens was confirmed by microcapillary reverse-phase high-performance liquid chromatography nano-electrospray tandem mass spectrometry. The tested rAbs frequently reacted with shared intracellular and extracellular self-antigens (for example, galectin-3). Furthermore, these self-antigens induced BCR signaling in B cells expressing cognate surface immunoglobulins derived from OAEMZLs. These findings indicate that interactions between self-antigens and cognate OAEMZL tumor-derived BCRs are functional, inducing intracellular signaling. Overall, our findings suggest that self-antigen-induced BCR stimulation may be implicated in the pathogenesis of C. psittaci-negative OAEMZLs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08876924
Volume :
29
Issue :
7
Database :
Academic Search Index
Journal :
Leukemia (08876924)
Publication Type :
Academic Journal
Accession number :
103702282
Full Text :
https://doi.org/10.1038/leu.2015.39