4.6 Article

CD40L-Stimulated B Lymphocytes Are Polarized toward APC Functions after Exposure to IL-4 and IL-21

Journal

JOURNAL OF IMMUNOLOGY
Volume 207, Issue 1, Pages 77-89

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.2001173

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Funding

  1. Natural Sciences and Engineering Research Council of Canada [RGPIN-2016-05376]
  2. Quebec Cell, Tissue and Gene Therapy Network - TheCell (a thematic network - Le Fonds de Recherche du Quebec - Sante [FRQS])
  3. Institut du Cancer de Montreal through Canderel scholarships
  4. FRQS
  5. Canadian Institutes of Health Research
  6. Roses of Hope Foundation

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The research revealed that IL-21 and Combo IL-4 CD40-B cells have high proliferative capacity, promoting T cell activation and proliferation, while IL-21 CD40-B cells tended to differentiate into antibody-secreting plasma cells. Stimulation of B cells with CD40L, IL-4, and IL-21 allows for the fast generation of high numbers of efficient antigen-presenting cells, offering potential tools for cancer immunotherapy and other clinical applications.
B lymphocytes have multiple functions central to humoral immunity, including Ag presentation to T cells, cytokine secretion, and differentiation into Ab-secreting plasma cells. In vitro expansion of human B cells by continuous IL-4 stimulation and engagement of their CD40 receptor by CD40L has allowed the use of these IL-4-CD40-B cells in research for the induction of Ag-specific T cell immune responses. However, in vivo, follicular helper T cells also influence B cell activity through the secretion of IL-21. The impact of both cytokines on multiple B cell functions is not clearly defined. To further understand these cytokines in CD40-B cell biology, we stimulated CD40-B cells with IL-4 or IL-21 or both (Combo) and characterized the proliferation, subsets, and functions of these cells. We demonstrate that IL-21- and Combo-CD40-B cells are highly proliferative cells that can be rapidly expanded to high numbers. We show that IL-21-CD40-B cells polarize to Ab-secreting plasma cells, whereas IL-4- and Combo-CD40-B cells are mostly activated mature B cells that express molecules associated with favorable APC functions. We further demonstrate that both IL-4- and Combo-CD40-B cells are efficient in promoting T cell activation and proliferation compared with IL-21-CD40-B cells. Thus, our study provides a better appreciation of CD40-B cell plasticity and biology. In addition, the stimulation of B cells with CD40L, IL-4, and IL-21 allows for the fast generation of high numbers of efficient APC, therefore providing a prospective tool for research and clinical applications such as cancer immunotherapy.

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