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. 2012 Jun 22;9:126. doi: 10.1186/1743-422X-9-126

Table 1.

Interaction of HCV proteins with PRRs

HCV Proteins PRRs Interaction of HCV proteins with PRRs Escape from innate immune system Escape from adaptive immune system
Core
TLR2
Induction of TLR2 homotolerance
Serum derived or recombinant core does not recognize TLR2
Inline graphic
 
 
Induction of TLR2 crosstolerance with TLR4
Monomeric Core recognize core
 
 
 
TLR1 or TLR6 are used as coreceptors with TLR2
Net Effect = Delayed Immune Response
 
NS3/4A
TLR3
Block TRIF and Cadif (adapter proteins) in down-stream signaling pathways of TLR3 and RIG-1 respectively
TLR3 and RIG-1 pathways are not activated until sufficient amount of dsRNA is produced, thus delaying innate immune response
Inline graphic
 
RIG-1
 
 
 
 
TLR2
 
 
 
 
 
TLR1 or TLR6 are used as coreceptors with TLR2
 
 
NS5A
TLR4
Increases TLR4 expressions
Block MyD88 (adapter protein) of TLR4 signaling pathway
Inline graphic
 
 
 
Also downregulates the expression of NFkB, MD2, CD14 and IRF3
 
 
 
 
Increases secretion of IL6, IFNβ, TGFβ and IL10
 
      Suppresses IL12 secretion