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. 2023 Jun 30;45(7):5534–5557. doi: 10.3390/cimb45070350

Table 1.

Types of TLRs described as associated with CD and UC. CS: cell surface; IC: intracellular; Mø: Monocytes/macrophages; B: B lymphocytes; MCs: mast cells; N: neutrophils; DCs: dendritic cells; IECs: intestinal epithelial cells. Data reported in table were collected from [45,46,47].

TLR Adapter Compartments Ligands Cell Types Main Alterations in IBD
TLR1 MyD88/TRIAP CS Di- and tri-acylated lipopeptides Mø, B, MCs No variation in IBD
TLR2 MyD88/TRIAP CS Bacterial lipoproteins or lipopeptides Mø, B, MCs Increased in active UC
TLR3 TRIF IC Double-stranded RNA (viral infection) Mø, B, MCs, N, Myeloid DCs, IECs Increased in active UC and CD
TLR4 MyD88/TRIAP, TRIF/TRAM CS LPS, free fatty acids Mø, B, MCs, N, Myeloid DCs, IECs Increased in UC and CD
TLR5 MyD88 CS Bacterial flagellins Mø, Myeloid DCs, IECs Decreased in CD
TLR6 MyD88/TRAF6 and NF-κB pathway CS Di- and tri-acylated lipopeptides Mø, B, MCs Increased in UC
TLR7 MyD88 IC/Endosomal Single stranded RNA (viral inflammation) Increased in UC
TLR8 MyD88 IC/endosomal RNA degradation products specific to microorganism (GU-rich single stranded RNA) Mø, DCs Increased in UC
TLR9 MyD88/TRAF6 IC Nucleid acid Mø, B, plasmacytoid DCs Increased in UC