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Ligation of CD40 on dendritic cells triggers production of high levels of interleukin-12 and enhances T cell stimulatory capacity: T-T help via APC activation.

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TLDR
It is found that ligation of CD40 by CD40L triggers the production of extremely high levels of bioactive IL-12, which is the most potent stimulus in upregulating the expression of ICAM-1, CD80, and CD86 molecules on DCs.
Abstract
We investigated the possibility that T helper cells might enhance the stimulatory function of dendritic cells (DCs). We found that ligation of CD40 by CD40L triggers the production of extremely high levels of bioactive IL-12. Other stimuli such as microbial agents, TNF-alpha or LPS are much less effective or not at all. In addition, CD40L is the most potent stimulus in upregulating the expression of ICAM-1, CD80, and CD86 molecules on DCs. These effects of CD40 ligation result in an increased capacity of DCs to trigger proliferative responses and IFN-gamma production by T cells. These findings reveal a new role for CD40-CD40L interaction in regulating DC function and are relevant to design therapeutic strategies using cultured DCs.

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Journal ArticleDOI

Dendritic cells and the control of immunity

TL;DR: Once a neglected cell type, dendritic cells can now be readily obtained in sufficient quantities to allow molecular and cell biological analysis and the realization that these cells are a powerful tool for manipulating the immune system is realized.
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Interleukin-12 and the regulation of innate resistance and adaptive immunity

TL;DR: The understanding of the relative roles of IL-12 and other factors in TH1-type maturation of both CD4+ and CD8+ T cells is discussed here, including the participation in this process ofIL-23 and IL-27, two recently discovered members of the new family of heterodimeric cytokines.
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Tolerogenic dendritic cells.

TL;DR: It is suggested that several clinical situations, including autoimmunity and certain infectious diseases, can be influenced by the antigen-specific tolerogenic role of DCs.
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T-cell help for cytotoxic T lymphocytes is mediated by CD40–CD40L interactions

TL;DR: In this paper, it was shown that signalling through CD40 can replace CD4+ T-helper cells in priming of helper-dependent CD8+ CTL responses.
Journal ArticleDOI

A conditioned dendritic cell can be a temporal bridge between a CD4 + T-helper and a T-killer cell

TL;DR: It is found that the three cells need not meet simultaneously but that the helper cell can first engage and ‘condition’ the dendritic cell, which then becomes empowered to stimulate a killer cell.
References
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Journal ArticleDOI

Dendritic cells as antigen presenting cells in vivo.

TL;DR: The specialized features of dendritic cells as antigen-presenting cells in selecting rare clones of antigen-specific T cells and activating them in vivo are described.
Journal ArticleDOI

Myeloma based expression system for production of large mammalian proteins.

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Uptake of microparticle‐adsorbed protein antigen by bone marrow‐derived dendritic cells results in up‐regulation of interleukin‐1α and interleukin‐12 p40/p35 and triggers prolonged, efficient antigen presentation

TL;DR: Using dendritic cells generated in vitro by culture of mouse bone marrow in the presence of low doses of recombinant mouse granulocyte/macrophage colony‐stimulating factor, it is found that discrete maturation stages of these cells can be distinguished which were correlated with defined functional capabilities.
Journal ArticleDOI

CD40 ligand-independent B cell activation revealed by CD40 ligand-deficient T cell clones: evidence for distinct activation requirements for antibody formation and B cell proliferation.

TL;DR: The capacity of CD40 ligand (CD40L)‐negative T cell clones to activate human B cells is reported, and the signal provided by the negative clones is synergistic with that derived from a CD40L transfectant, and restores B cell proliferation to normal levels, showing that CD40 L‐negativeT cell clones are not inherently inhibitory for B cells.
Journal ArticleDOI

Dendritic cells as antigen-presenting cells in vivo

TL;DR: The specialized features of dendritic cells as antigen‐presenting cells in selecting rare clones of antigen‐specific T cells and activating them in vivo are described.
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