Artikel ; Online: Immunogenomics of Killer Cell Immunoglobulin-Like Receptor (KIR) and HLA Class I: Coevolution and Consequences for Human Health.
The journal of allergy and clinical immunology. In practice
2022 Band 10, Heft 7, Seite(n) 1763–1775
Abstract: Interactions of killer cell immunoglobin-like receptors (KIR) with human leukocyte antigens (HLA) class I regulate effector functions of key cytotoxic cells of innate and adaptive immunity. The extreme diversity of this interaction is genetically ... ...
Abstract | Interactions of killer cell immunoglobin-like receptors (KIR) with human leukocyte antigens (HLA) class I regulate effector functions of key cytotoxic cells of innate and adaptive immunity. The extreme diversity of this interaction is genetically determined, having evolved in the ever-changing environment of pathogen exposure. Diversity of KIR and HLA genes is further facilitated by their independent segregation on separate chromosomes. That fetal implantation relies on many of the same types of immune cells as infection control places certain constraints on the evolution of KIR interactions with HLA. Consequently, specific inherited combinations of receptors and ligands may predispose to specific immune-mediated diseases, including autoimmunity. Combinatorial diversity of KIR and HLA class I can also differentiate success rates of immunotherapy directed to these diseases. Progress toward both etiopathology and predicting response to therapy is being achieved through detailed characterization of the extent and consequences of the combinatorial diversity of KIR and HLA. Achieving these goals is more tractable with the development of integrated analyses of molecular evolution, function, and pathology that will establish guidelines for understanding and managing risks. Here, we present what is known about the coevolution of KIR with HLA class I and the impact of their complexity on immune function and homeostasis. |
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Mesh-Begriff(e) | Evolution, Molecular ; Genes, MHC Class I/genetics ; Genes, MHC Class I/immunology ; HLA Antigens/genetics ; HLA Antigens/immunology ; Health ; Histocompatibility Antigens Class I/genetics ; Histocompatibility Antigens Class I/immunology ; Humans ; Immunogenetic Phenomena/genetics ; Killer Cells, Natural/immunology ; Receptors, KIR/genetics ; Receptors, KIR/immunology |
Chemische Substanzen | HLA Antigens ; Histocompatibility Antigens Class I ; Receptors, KIR |
Sprache | Englisch |
Erscheinungsdatum | 2022-05-10 |
Erscheinungsland | United States |
Dokumenttyp | Journal Article ; Research Support, N.I.H., Extramural |
ZDB-ID | 2843237-X |
ISSN | 2213-2201 ; 2213-2198 |
ISSN (online) | 2213-2201 |
ISSN | 2213-2198 |
DOI | 10.1016/j.jaip.2022.04.036 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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