TY - JOUR
T1 - Principles of intracellular viral recognition
AU - Saito, Takeshi
AU - Gale, Michael
PY - 2007/2
Y1 - 2007/2
N2 - In mammalian cells, the products of microbial infection are recognized by pathogen recognition receptor (PRR) proteins. Virus recognition is mediated in part by PRRs that comprise a subset of Toll-like receptors or a family of RNA helicases, the latter of which contain caspase activation and recruitment domains, both of which induce interferons α and β and antiviral immune defenses. Recent studies show that PRR engagement of specific pathogen-associated molecular patterns (PAMPs) within viral products, including viral proteins and nucleic acid, is facilitated by the discrete subcellular distribution of PRRs to sites that intersect with processes of virus entry and replication. PAMP structure and the subcellular context of PRR distribution form a basis of self versus nonself discrimination during the antiviral response. Understanding the virus/host interface of PRR function and PAMP recognition will advance therapeutic strategies for immune response regulation.
AB - In mammalian cells, the products of microbial infection are recognized by pathogen recognition receptor (PRR) proteins. Virus recognition is mediated in part by PRRs that comprise a subset of Toll-like receptors or a family of RNA helicases, the latter of which contain caspase activation and recruitment domains, both of which induce interferons α and β and antiviral immune defenses. Recent studies show that PRR engagement of specific pathogen-associated molecular patterns (PAMPs) within viral products, including viral proteins and nucleic acid, is facilitated by the discrete subcellular distribution of PRRs to sites that intersect with processes of virus entry and replication. PAMP structure and the subcellular context of PRR distribution form a basis of self versus nonself discrimination during the antiviral response. Understanding the virus/host interface of PRR function and PAMP recognition will advance therapeutic strategies for immune response regulation.
UR - https://www.scopus.com/pages/publications/33846100059
UR - https://www.scopus.com/inward/citedby.url?scp=33846100059&partnerID=8YFLogxK
U2 - 10.1016/j.coi.2006.11.003
DO - 10.1016/j.coi.2006.11.003
M3 - Review article
C2 - 17118636
AN - SCOPUS:33846100059
SN - 0952-7915
VL - 19
SP - 17
EP - 23
JO - Current Opinion in Immunology
JF - Current Opinion in Immunology
IS - 1
ER -