Another View of T Cell Antigen Recognition: Cooperative Engagement of Glycolipid Antigens by Va14Ja18 Natural TCR
Journal of Immunology, ISSN: 0022-1767, Vol: 171, Issue: 9, Page: 4539-4551
2003
- 76Citations
- 19Captures
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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
- Citations76
- Citation Indexes76
- 76
- CrossRef70
- Captures19
- Readers19
- 19
Article Description
Va14Ja18 natural T (iNKT) cells rapidly elicit a robust effector response to different glycolipid Ags, with distinct functional outcomes. Biochemical parameters controlling iNKT cell function are partly defined. However, the impact of iNKT cell receptor β-chain repertoire and how α-galactosylceramide (α-GalCer) analogues induce distinct functional responses have remained elusive. Using altered glycolipid ligands, we discovered that the Vb repertoire of iNKT cells impacts recognition and Ag avidity, and that stimulation with suboptimal avidity Ag results in preferential expansion of high-affinity iNKT cells. iNKT cell proliferation and cytokine secretion, which correlate with iNKT cell receptor down-regulation, are induced within narrow biochemical thresholds. Multimers of CD1d1-αGalCer- and αGalCer analogue-loaded complexes demonstrate cooperative engagement of the Va14Ja18 iNKT cell receptor whose structure and/ or organization appear distinct from conventional αβ TCR. Our findings demonstrate that iNKT cell functions are controlled by affinity thresholds for glycolipid Ags and reveal a novel property of their Ag receptor apparatus that may have an important role in iNKT cell activation.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=10744225154&origin=inward; http://dx.doi.org/10.4049/jimmunol.171.9.4539; http://www.ncbi.nlm.nih.gov/pubmed/14568927; https://journals.aai.org/jimmunol/article/171/9/4539/78269/Another-View-of-T-Cell-Antigen-Recognition; https://dx.doi.org/10.4049/jimmunol.171.9.4539; http://europepmc.org/abstract/med/14568927; http://www.jimmunol.org/cgi/doi/10.4049/jimmunol.171.9.4539; http://www.jimmunol.org/content/171/9/4539; http://www.jimmunol.org/content/171/9/4539.abstract; http://www.jimmunol.org/content/171/9/4539.full.pdf; http://www.jimmunol.org/lookup/doi/10.4049/jimmunol.171.9.4539; https://www.jimmunol.org/content/171/9/4539; https://www.jimmunol.org/content/171/9/4539.abstract; https://www.jimmunol.org/content/jimmunol/171/9/4539.full.pdf; http://www.jimmunol.org/cgi/content/full/171/9/4539
Oxford University Press (OUP)
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