Related Experiment Video
Updated: Aug 14, 2026

Induction of Murine Intestinal Inflammation by Adoptive Transfer of Effector CD4+CD45RBhigh T Cells into Immunodeficient Mice
Published on: April 21, 2015
Activated CD19+ B cell lamina propria lymphocytes in ulcerative colitis
1Department of Medicine, University of Alberta, Edmonton, Canada.
Insights
B cells in ulcerative colitis (UC) show higher activation markers, including CD71, CD25, and 4F2, compared to Crohn's disease or normal tissues. This suggests increased transitional B cells in UC, potentially linking B cell activation to immunoglobulin differences in inflammatory bowel disease.
Area of Science:
- Immunology
- Gastroenterology
- Cell Biology
Background:
- Isotype differences in immunoglobulin production by lamina propria lymphocytes (LPL) are known in ulcerative colitis (UC) and Crohn's disease (CD).
- B cell activation differences between normal individuals and patients with inflammatory bowel disease (IBD) have not been well-described.
Purpose of the Study:
- To investigate and compare B cell activation in the LPL of patients with UC, CD, and normal controls.
- To explore the relationship between B cell activation status and immunoglobulin production in IBD.
Main Methods:
- Flow cytometry was used to analyze B cell activation markers (CD71, CD25, 4F2) on LPLs.
- Transitional B cells were identified by co-expression of CD45RA and CD45RO.
Main Results:
- UC LPLs exhibited significantly higher expression of CD71, CD25, and 4F2 on CD19+ B cells compared to CD and normal LPLs.
- A greater proportion of transitional B cells (CD45RA+/CD45RO+) was observed in UC LPLs.
- Findings support the role of CD45 isoform transition in CD19 B cell activation.
Conclusions:
- UC LPL B cells display a heightened state of activation compared to those in CD and normal individuals.
- Increased B cell activation in UC may contribute to distinct immunoglobulin production patterns observed in IBD.
- These findings may hold diagnostic and pathophysiological significance for IBD research.
Abstract:
Although isotype differences in lamina propria lymphocyte (LPL) immunoglobulin production has been recognized between normal, ulcerative colitis (UC) and Crohn's patients, differences in B cell activation between these conditions has not been described. Using flow cytometry, we studied B cell LPL activation using the CD71 (transferrin receptor), CD25 (interleukin-2 receptor) and 4F2 (early B and T cell activation marker) monoclonal antibodies. CD19+ B cells from patients with UC had relatively increased expression of CD71, CD25 and 4F2 compared with patients with Crohn's disease or normal mucosa. This finding corresponds to an increased proportion of transitional (activated) B cells as defined by the co-expression of CD45RA and CD45RO found in UC LPL compared with normal or Crohn's patient LPL. Such data may identify an important link between the cellular state of activation of UC LPL B cells and the differences in immunoglobulin production between the inflammatory bowel diseases and normal intestine. Such findings may have further diagnostic or pathophysiologic importance in the study of these diseases. This work also provides further support for the CD45 transition of CD19 B cells from the high to low molecular weight isoform.
Related Concept Videos
Drugs for Treatment of Ulcerative Colitis in IBD
Inflammatory Bowel Disease I: Ulcerative Colitis
Inflammatory bowel disease, or IBD, encompasses a group of disorders characterized by chronic inflammation or ulceration of the gastrointestinal tract.
Risk Factors
The exact cause of IBD remains unclear, although it is believed to be due to a mix of genetic, environmental, microbial, and immune factors. Genetic factors are significant in determining susceptibility to IBD, with family history being a critical risk factor. Individuals with a first-degree relative who has IBD are at...
Inflammatory Bowel Disease I: Introduction
Inflammatory Bowel Disease II: Ulcerative Colitis
Inflammatory Bowel Disease III: Crohn's Disease
Inflammatory Bowel Disease IV: Clinical Manifestations

