4-1BB-ligand is regulated on human dendritic cells and induces the production of IL-12
Cellular Immunology, ISSN: 0008-8749, Vol: 226, Issue: 1, Page: 37-44
2003
- 62Citations
- 31Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations62
- Citation Indexes62
- 62
- CrossRef53
- Captures31
- Readers31
- 31
Article Description
Co-stimulation via 4-1BB and its ligand 4-1BB ligand (4-1BB-L) plays an important role in cytotoxic and pro-inflammatory immune responses. 4-1BB-L is generally described on activated antigen-presenting cells but there is limited information on its expression and function in human dendritic cells (DC). We herein compared purified CD1a+CD14− DC issued from monocytes or from hematopoietic progenitor cells (HPC). These DC expressed 4-1BB-L mRNA transcripts with highest cell surface levels on HPC-derived DC cultured with IL-1. Pro-inflammatory activation, particularly CD40 ligand+IL-1, up-regulated 4-1BB-L on DC. We confirmed reverse signaling via 4-1BB-L as immobilized 4-1BB in conjunction with CD40-L, enhanced IL-12β mRNA and the secretion of IL-12 p70 in various APC, including monocytes. Altogether, DC may differ in T cell co-stimulation properties due to variable and regulated levels of 4-1BB-L. Data illustrate reciprocal stimulations between T cells and APC via up-regulated receptor/ligands and production of key cytokines that consolidate cellular immune responses.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0008874903002673; http://dx.doi.org/10.1016/j.cellimm.2003.11.003; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=1642432076&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/14746806; https://linkinghub.elsevier.com/retrieve/pii/S0008874903002673; https://dx.doi.org/10.1016/j.cellimm.2003.11.003
Elsevier BV
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