A common inhibitory receptor for major histocompatibility complex class I molecules on human lymphoid and myelomonocytic cells
Journal of Experimental Medicine, ISSN: 0022-1007, Vol: 186, Issue: 11, Page: 1809-1818
1997
- 836Citations
- 189Captures
- 8Mentions
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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
- Citations836
- Citation Indexes831
- 831
- CrossRef735
- Patent Family Citations4
- Patent Families4
- Policy Citations1
- Policy Citation1
- Captures189
- Readers189
- 189
- Mentions8
- References8
- Wikipedia8
Article Description
Natural killer (NK) cell-mediated lysis is negatively regulated by killer cell inhibitory receptors specific for major histocompatibility complex (MHC) class I molecules. In this study, we characterize a novel inhibitory MHC class I receptor of the immunoglobulin-superfamily, expressed not only by subsets of NK and T cells, but also by B cells, monocytes, macrophages, and dendritic cells. This receptor, called Ig-like transcript (ILT)2, binds MHC class I molecules and delivers a negative signal that inhibits killing by NK and T cells, as well as Ca mobilization in B cells and myelomonocytic cells triggered through the B cell antigen receptor and human histocompatibility leukocyte antigens (HLA)-DR, respectively. In addition, myelomonocytic cells express receptors homologous to ILT2, which are characterized by extensive polymorphism and might recognize distinct HLA class I molecules. These results suggest that diverse leukocyte lineages have adopted recognition of self-MHC class I molecules as a common strategy to control cellular activation during an immune response.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0030819308&origin=inward; http://dx.doi.org/10.1084/jem.186.11.1809; http://www.ncbi.nlm.nih.gov/pubmed/9382880; https://rupress.org/jem/article/186/11/1809/25363/A-Common-Inhibitory-Receptor-for-Major; http://www.jem.org/lookup/doi/10.1084/jem.186.11.1809; http://jem.rupress.org/content/186/11/1809
Rockefeller University Press
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