Phenotypic characteristics of B cells in Behcet's disease: Increased activity in B cell subsets

Citation
E. Eksioglu-demiralp et al., Phenotypic characteristics of B cells in Behcet's disease: Increased activity in B cell subsets, J RHEUMATOL, 26(4), 1999, pp. 826-832
Citations number
50
Categorie Soggetti
Rheumatology,"da verificare
Journal title
JOURNAL OF RHEUMATOLOGY
ISSN journal
0315162X → ACNP
Volume
26
Issue
4
Year of publication
1999
Pages
826 - 832
Database
ISI
SICI code
0315-162X(199904)26:4<826:PCOBCI>2.0.ZU;2-T
Abstract
Objective. Increased numbers of spontaneous Ig secreting B cells and elevat ed immunoglobulin levels have been described in Behcet's disease (BD), in a ddition to changes in numbers and activities of T cells, natural killer cel ls, and monocyte-macrophages. We investigated other characteristics of B ce lls in BD. Methods. B lymphocyte subsets (CD19+CD5+, CD19+CD13+, CD19+CD28+, CD19+CD33 +, CD19+CD80+, CD5+CD19+CD45RA+, CD5+CD19+CD45RO+) were phenotypically eval uated in 50 patients with ED, 80 healthy subjects, and 20 other patients wi th rheumatoid arthritis (RA), systemic lupus erythematosus (SLE); and sepsi s. Results. Although the B cell number (CD19+) was normal, CD13 and CD33 posit ive B cells were more numerous in ED and sepsis compared to healthy control s and patients with RA and SLE. The percentage of CD45RO positive B cells w as higher in both ED and sepsis, while the percentage of CD80 positive B ce lls was high only in ED. There was no increase in the CD5+CD19+ B cell subs et, previously shown to be increased in several autoimmune diseases. Naive (CD45RA) and memory (CD45RO) status of CD5+CD19+ and CD5-CD19+ B cells show ed that CD45RA expression was higher in CD5+CD19+ B cells, whereas expressi on of both CD45RA and CD45RO was higher in the CD5-CD19+ B cell group compa red with healthy controls. Conclusion. Although the total B cell number was normal, increased levels o f activated and memory B cell subsets suggest a modified B cell function in BI, which may be related to a weak stimulus by an unknown external antigen .