| Literature DB >> 31823416 |
A Ali Zirakzadeh1,2, Amir Sherif2, Robert Rosenblatt2, Emma Ahlén Bergman1, Max Winerdal1, David Yang1, Johanna Cederwall2, Vivianne Jakobsson1, Martin Hyllienmark1, Ola Winqvist3, Per Marits1.
Abstract
Tumour infiltrating B cells and CD38+ plasma cells have been correlated with survival in different malignancies but their role in urinary bladder cancer is unclear. IL-10 is a multifunctional cytokine with both anti-inflammatory and immunostimulatory properties, that can be released by regulatory B cells (Bregs). We have stained paraffin-embedded tumour sections from 31 patients with invasive urothelial urinary bladder cancer with respect to CD20+ B cells, CD38+ cells, IL-10-expressing cells, IgG, C1q and C3a and analysed the impact of these markers on survival. Interestingly, we observe tumour-associated CD20+ B cells forming follicle-like structures in tumours of some patients. We demonstrate that follicle-like structures, tumour-associated CD38+ cells, IL-10 produced by non-B cells, tumour infiltrating IgG and activation of the complement system, may associate to longer survival of urinary bladder cancer patients. IL-10 expression by tumour-associated Bregs may instead negatively affect prognosis. More research is needed to fully understand the role of B cells and IL-10 in urinary bladder cancer.Entities:
Keywords: follicle-like structures; tumour-associated B cells; urinary bladder cancer
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Year: 2019 PMID: 31823416 DOI: 10.1111/sji.12830
Source DB: PubMed Journal: Scand J Immunol ISSN: 0300-9475 Impact factor: 3.487