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10.1016/j.coi.2021.04.005

http://scihub22266oqcxt.onion/10.1016/j.coi.2021.04.005
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suck abstract from ncbi


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pmid34004375      Curr+Opin+Immunol 2021 ; 72 (ä): 126-134
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  • Membrane cofactor protein (MCP; CD46): deficiency states and pathogen connections #MMPMID34004375
  • Liszewski MK; Atkinson JP
  • Curr Opin Immunol 2021[Oct]; 72 (ä): 126-134 PMID34004375show ga
  • Membrane cofactor protein (MCP; CD46), a ubiquitously expressed complement regulatory protein, serves as a cofactor for serine protease factor I to cleave and inactivate C3b and C4b deposited on host cells. However, CD46 also plays roles in human reproduction, autophagy, modulating T cell activation and effector functions and is a member of the newly identified intracellular complement system (complosome). CD46 also is a receptor for 11 pathogens ('pathogen magnet'). While CD46 deficiencies contribute to inflammatory disorders, its overexpression in cancers and role as a receptor for some adenoviruses has led to its targeting by oncolytic agents and adenoviral-based therapeutic vectors, including coronavirus disease of 2019 (COVID-19) vaccines. This review focuses on recent advances in identifying disease-causing CD46 variants and its pathogen connections.
  • |Animals[MESH]
  • |Autophagy[MESH]
  • |COVID-19 Vaccines/*immunology[MESH]
  • |COVID-19/*immunology[MESH]
  • |Complement Activation[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Lymphocyte Activation[MESH]
  • |Membrane Cofactor Protein/genetics/*metabolism[MESH]
  • |Oncolytic Virotherapy[MESH]
  • |Polymorphism, Genetic[MESH]
  • |Reproduction[MESH]
  • |SARS-CoV-2/*physiology[MESH]


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