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10.1002/jmv.27265

http://scihub22266oqcxt.onion/10.1002/jmv.27265
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34375002!ä!34375002

suck abstract from ncbi

pmid34375002      J+Med+Virol 2021 ; 93 (11): 6116-6123
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  • Viral proteins recognized by different TLRs #MMPMID34375002
  • Zhou R; Liu L; Wang Y
  • J Med Virol 2021[Nov]; 93 (11): 6116-6123 PMID34375002show ga
  • Virus invasion activates the host's innate immune response, inducing the production of numerous cytokines and interferons to eliminate pathogens. Except for viral DNA/RNA, viral proteins are also targets of pattern recognition receptors. Membrane-bound receptors such as Toll-like receptor (TLR)1, TLR2, TLR4, TLR6, and TLR10 relate to the recognition of viral proteins. Distinct TLRs perform both protective and detrimental roles for a specific virus. Here, we review viral proteins serving as pathogen-associated molecular patterns and their corresponding TLRs. These viruses are all enveloped, including respiratory syncytial virus, hepatitis C virus, measles virus, herpesvirus human immunodeficiency virus, and coronavirus, and can encode proteins to activate innate immunity in a TLR-dependent way. The TLR-viral protein relationship plays an important role in innate immunity activation. A detailed understanding of their pathways contributes to a novel direction for vaccine development.
  • |*Immunity, Innate[MESH]
  • |Animals[MESH]
  • |HIV/immunology/metabolism/pathogenicity[MESH]
  • |Hepacivirus/immunology/metabolism/pathogenicity[MESH]
  • |Herpesviridae/immunology/metabolism/pathogenicity[MESH]
  • |Humans[MESH]
  • |Measles virus/immunology/metabolism/pathogenicity[MESH]
  • |Pathogen-Associated Molecular Pattern Molecules/chemistry/*metabolism[MESH]
  • |Respiratory Syncytial Viruses/immunology/metabolism/pathogenicity[MESH]
  • |SARS-CoV-2/immunology/metabolism/pathogenicity[MESH]
  • |Toll-Like Receptors/*immunology/*metabolism[MESH]
  • |Viral Proteins/chemistry/*metabolism[MESH]
  • |Virus Diseases/*immunology/virology[MESH]


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