The dichotomy of regulatory B cells in cancer versus allergic disease

Author:

Dang Melissa1,Yu Justin2ORCID,Galant‐Swafford Jessica3,Karam Sana D.4ORCID

Affiliation:

1. Department of Internal Medicine Sky Ridge Medical Center Lone Tree Colorado USA

2. Department of Otolaryngology—Head and Neck Surgery University of Colorado Anschutz Medical Campus Aurora Colorado USA

3. Division of Allergy & Clinical Immunology National Jewish Health Denver Colorado USA

4. Department of Radiation Oncology University of Colorado Anschutz Medical Campus Aurora Colorado USA

Abstract

AbstractRegulatory B cells (Bregs) are an immunosuppressive cell phenotype that affects the immune system by limiting the inflammatory cascade. Dysregulation of Bregs can interestingly play a dichotomous role in the pathophysiology of many diseases and is especially highlighted when examining cancer pathology compared to allergic disease. This study reviews the existing literature on Bregs and compares their role in allergic disease in contrast to cancer development. Upregulation of Bregs in cancer states has been associated with poor prognostic outcomes across various cancer types, and Breg proliferation was associated with chronic interferon signaling, activation of the BCR–BTK (B cell receptor‐Bruton's tyrosine kinase) pathway, and release of C–X–C motif ligand 13. In contrast, Breg dysfunction has been identified as a key mechanism in many allergic diseases, such as allergic asthma, allergic rhinitis, atopic dermatitis, and contact dermatitis. Development of Breg‐targeted immunotherapies is currently at the preclinical level, but strategies differentially focus on Breg depletion in cancer versus Breg stimulation in allergy. Our review highlights the divergent functions that Bregs play in cancer compared to allergy. We conclude that natural homeostasis hinges on a fine balance between the dichotomous role of Bregs—over or underactivation can result in a pathological state.

Publisher

Wiley

Subject

Cancer Research,Molecular Biology

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