Hongbing Yang, Margarida Rei, Simon Brackenridge, Elena Brenna, Hong Sun, Shaheed Abdulhaqq, Michael K P Liu, Weiwei Ma, Prathiba Kurupati, Xiaoning Xu, Vincenzo Cerundolo, Edward Jenkins, Simon J Davis, Jonah B Sacha, Klaus Früh, Louis J Picker, Persephone Borrow, Geraldine M Gillespie, Andrew J McMichael. Sci Immunol 2021
Times Cited: 15
Times Cited: 15
Times Cited
Times Co-cited
Similarity
Broadly targeted CD8⁺ T cell responses restricted by major histocompatibility complex E.
Scott G Hansen, Helen L Wu, Benjamin J Burwitz, Colette M Hughes, Katherine B Hammond, Abigail B Ventura, Jason S Reed, Roxanne M Gilbride, Emily Ainslie, David W Morrow,[...]. Science 2016
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Modulation of MHC-E transport by viral decoy ligands is required for RhCMV/SIV vaccine efficacy.
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Cytomegaloviral determinants of CD8+ T cell programming and RhCMV/SIV vaccine efficacy.
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HLA-E allelic variants. Correlating differential expression, peptide affinities, crystal structures, and thermal stabilities.
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Cytomegalovirus vectors violate CD8+ T cell epitope recognition paradigms.
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Human CD8+ T-cells recognizing peptides from Mycobacterium tuberculosis (Mtb) presented by HLA-E have an unorthodox Th2-like, multifunctional, Mtb inhibitory phenotype and represent a novel human T-cell subset.
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Alternative peptide repertoire of HLA-E reveals a binding motif that is strikingly similar to HLA-A2.
Margit H Lampen, Chopie Hassan, Marjolein Sluijter, Annemieke Geluk, Karin Dijkman, Jennifer M Tjon, Arnoud H de Ru, Sjoerd H van der Burg, Peter A van Veelen, Thorbald van Hall. Mol Immunol 2013
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Peptide Binding to HLA-E Molecules in Humans, Nonhuman Primates, and Mice Reveals Unique Binding Peptides but Remarkably Conserved Anchor Residues.
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Detailed and atypical HLA-E peptide binding motifs revealed by a novel peptide exchange binding assay.
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Mycobacterium tuberculosis peptides presented by HLA-E molecules are targets for human CD8 T-cells with cytotoxic as well as regulatory activity.
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Profound early control of highly pathogenic SIV by an effector memory T-cell vaccine.
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HLA-E is a major ligand for the natural killer inhibitory receptor CD94/NKG2A.
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Immune clearance of highly pathogenic SIV infection.
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Structural basis for a major histocompatibility complex class Ib-restricted T cell response.
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HLA-E-restricted recognition of cytomegalovirus-derived peptides by human CD8+ cytolytic T lymphocytes.
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Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding.
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The unconventional role of HLA-E: The road less traveled.
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Detailed characterization of human Mycobacterium tuberculosis specific HLA-E restricted CD8+ T cells.
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MHC-E-Restricted CD8+ T Cells Target Hepatitis B Virus-Infected Human Hepatocytes.
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The human major histocompatibility complex class Ib molecule HLA-E binds signal sequence-derived peptides with primary anchor residues at positions 2 and 9.
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A live-attenuated RhCMV/SIV vaccine shows long-term efficacy against heterologous SIV challenge.
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Epstein-Barr virus peptide presented by HLA-E is predominantly recognized by CD8(bright) cells in multiple sclerosis patients.
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HIV-1 infection leads to increased HLA-E expression resulting in impaired function of natural killer cells.
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The Role of MHC-E in T Cell Immunity Is Conserved among Humans, Rhesus Macaques, and Cynomolgus Macaques.
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HCMV triggers frequent and persistent UL40-specific unconventional HLA-E-restricted CD8 T-cell responses with potential autologous and allogeneic peptide recognition.
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A conserved energetic footprint underpins recognition of human leukocyte antigen-E by two distinct αβ T cell receptors.
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HLA-E-restricted HIV-1-specific CD8+ T cell responses in natural infection.
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Effector memory T cell responses are associated with protection of rhesus monkeys from mucosal simian immunodeficiency virus challenge.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.