Results 201 to 210 of about 183,897 (254)
Accurate multi-population imputation of MICA, MICB, HLA-E, HLA-F and HLA-G alleles from genome SNP data. [PDF]
Tammi S +5 more
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Mtb-Specific HLA-E-Restricted T Cells Are Induced during Mtb Infection but Not after BCG Administration in Non-Human Primates and Humans. [PDF]
Voogd L +14 more
europepmc +1 more source
Obtaining Gene-Modified HLA-E-Expressing Feeder Cells for Stimulation of Natural Killer Cells. [PDF]
Alekseeva NA +8 more
europepmc +1 more source
SARS-CoV-2 infection induces adaptive NK cell responses by spike protein-mediated induction of HLA-E expression. [PDF]
Hasan MZ +9 more
europepmc +1 more source
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HLA‐E and immunobiology of pregnancy
Tissue Antigens, 2006AbstractRecently, it has been suggested that non‐classical antigens such as human leukocyte antigen (HLA)‐G and HLA‐E may interact with KIR receptors of NK cells which results into downregulation of immune response and helps in the maintenance of pregnancy.
P, Tripathi, S, Naik, S, Agrawal
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HLA-E and HLA-E-Bound Peptides: Recognition by Subsets of NK and T Cells
Current Pharmaceutical Design, 2009In humans, major histocompatibility complex (MHC) class I molecules comprise the classical (class Ia) human leukocyte antigens (HLA)-A, -B, and -C, and the non-classical (class Ib) HLA-E, -F, -G and -H (HFE) molecules. The best-characterized MHC class Ib molecule is HLA-E. HLA-E was first described as a non-polymorphic ligand of the CD94/NKG2 receptors
PIETRA, GABRIELLA +3 more
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The involvement of HLA-E and -F in pregnancy
Journal of Reproductive Immunology, 2006The human MHC class I genes, HLA-E, -F and -G are referred to as non-classical or class Ib genes and are distinguished from their close relatives (the classical HLA class I genes) by expression patterns and low allelic polymorphism. To date, most studies that relate these molecules to the immunology of pregnancy have concerned only HLA-G.
Akiko, Ishitani +2 more
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2012
Human leukocyte antigen-E (HLA-E) is a non-classical HLA class I gene that shows a limited degree of polymorphism compared to the classical HLA genes. The HLA-E molecule can bind peptides derived from the leader sequence of various HLA class I alleles and some viral homologues, including CMV.
Nina, Lauterbach +2 more
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Human leukocyte antigen-E (HLA-E) is a non-classical HLA class I gene that shows a limited degree of polymorphism compared to the classical HLA genes. The HLA-E molecule can bind peptides derived from the leader sequence of various HLA class I alleles and some viral homologues, including CMV.
Nina, Lauterbach +2 more
openaire +2 more sources
Tissue Antigens, 2015
AbstractHuman Leukocyte Antigen (HLA)‐E is a low‐polymorphic non‐classical HLA class I molecule which plays a crucial role in immune surveillance by presentation of peptides to T and natural killer (NK) cells. HLA‐E polymorphism is related to HLA‐E surface expression and is associated with patient outcome after stem cell transplantation.
Lauterbach, N. +6 more
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AbstractHuman Leukocyte Antigen (HLA)‐E is a low‐polymorphic non‐classical HLA class I molecule which plays a crucial role in immune surveillance by presentation of peptides to T and natural killer (NK) cells. HLA‐E polymorphism is related to HLA‐E surface expression and is associated with patient outcome after stem cell transplantation.
Lauterbach, N. +6 more
openaire +3 more sources
Human Immunology, 2000
The interaction of HLA-E with CD94/NKG2A is dependant on the binding of HLA class I signal sequence derived peptides to HLA-E. In the caucasoid population two HLA-E alleles are observed at equal frequencies. Here we study the functional differences between the two HLA-E molecules with regard to cell surface expression, peptide binding, and potential to
S, Maier +3 more
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The interaction of HLA-E with CD94/NKG2A is dependant on the binding of HLA class I signal sequence derived peptides to HLA-E. In the caucasoid population two HLA-E alleles are observed at equal frequencies. Here we study the functional differences between the two HLA-E molecules with regard to cell surface expression, peptide binding, and potential to
S, Maier +3 more
openaire +2 more sources

