Review Article

Current and Emerging Evidence for Toll-Like Receptor Activation in Sjögren’s Syndrome

Table 3

Systemic TLR dysregulation in human SS.

Cell typeTLRResultsRefs

PBMCs2(i) PBMCs from pSS patients are more responsive to TLR2, TLR4, and TLR6 agonists than those from healthy controls
(ii) TLR2, TLR4, and TLR6 agonists show additive effect in induction of IL-23 and IL-17 secretion in cultured PBMCs from pSS patients
[49]
PBMCs5(i) Reduced protein expression[63]
PBMCs7(i) Increased gene expression[78]
PBMCs7(i) Increased protein expression[63]
B cells7(i) Stimulation with TLR7 agonist (CL264) causes elevated IFNα secretion[80]
CD14+ monocytes7(i) Increased expression of TLR7 in pSS patients with a positive type I IFN signature[77]
PBMCs8(i) Elevated gene expression[63]
moDCs7/8(i) Increased maturation in moDCs derived from pSS patients following stimulation with TLR7/8 agonist (CL097)[82]
B cells7, 9(i) Stimulation of naïve B cells from pSS patients with TLR7 (imiquimod) or TLR9 (CpG) agonists causes increased plasma cell differentiation and class switching compared to controls[81]
CD14+ monocytes9(i) Decreased TLR9 expression in monocytes from both type I IFN-positive and IFN-negative pSS patients[77]
PBMCs9(i) Decreased gene expression[63]
PBMCs9(i) Increased gene expression[78]
PBMCs9(i) Enhanced secretion of IL-8, IL-15, IL-1RA, MCP-1, and IL-2R upon stimulation with TLR9 agonist CpG
(ii) TLR9 agonist (CpG) decreased CD80 and CD25 expression
[80]