CD1: antigen presentation and T cell function.

By M. Brigl, M. Brenner. Annual Review of Immunology, 2004

1,114 citations recorded by the source corpus.

Subfields: Immunology

View Paper: https://www.semanticscholar.org/paper/0ca6d474868bdc7d92bf5176a2eda95d42ccece8

How researchers see this paper

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In Immunology

1. M. Kronenberg
2. A. Bendelac
3. L. Teyton
4. K. Hoebe
5. B. Beutler
6. P. Savage
7. A. O’Garra
8. A. Peschel

Citations in the corpus

• Recognition of bacterial glycosphingolipids by natural killer T cells (2005, background): “jpg" NDATA ITEM> ]> Natural killer T (NKT) cells constitute a highly conserved T lymphocyte subpopulation that has the potential to regulate many types of immune responses through the rapid secretion of cytokine”
• Natural killer T cells recognize diacylglycerol antigens from pathogenic bacteria (2006, background): “Because V α 14 i NKT cells have been shown to participate in the protection of mice from bacterial infection”
• The biology of NKT cells. (2007, background): “CD1a, -b, and -c differ in their location in different endosomal compartments, in early recycling to late endosome and lysosome, and also in the architecture of their lipid-binding grooves, which suggests that each is specialized to capture different lipids in different endosomal compartments (44).”
• Teichoic acids and related cell-wall glycopolymers in Gram-positive physiology and host interactions (2008, background): “The CD1 family of molecules is able to present glycolipid antigens to CD1-restricted T cell”
• The emerging field of lipidomics (2005, background): “Many different classes of lipids, including phosphoinositols, sphingomyelin, mycolates, isoprenoids and lipoproteins, are known to bind to CD1 protein”
• The immune response in tuberculosis. (2013, background): “tuberculosis intersects the loading pathways of the CD1 molecules (213, 214).”
• Human Mucosal Associated Invariant T Cells Detect Bacterially Infected Cells (2010, background): “Furthermore, CD1-restricted T cells may be less frequent in the CD8 population [15].”