Functional insights into autoantibodies targeting muscarinic acetylcholine receptors in Sjögren's disease.

OBJECTIVES

G protein-coupled receptors (GPCRs) participate in various pathophysiological processes in Sjögren's disease (SjD); in particular, autoantibodies against muscarinic acetylcholine receptor 3 (M3R) inhibit the secretion of saliva and tears by exocrine glands. We aimed to identify autoantibodies targeting other muscarinic receptors in SjD and assess their potential functional relevance to signalling pathways.

METHODS

Autoantibodies against all muscarinic acetylcholine receptor subtypes were investigated in the serum of patients with SjD (n = 347) using enzyme-linked immunosorbent assays (ELISAs). Healthy controls (HCs; n = 50), patients with non-Sjögren's sicca syndrome (NSS; n = 44), and patients with other autoimmune diseases (AIDs; n = 67) served as controls. To analyse the functional role of muscarinic receptor autoantibodies against muscarinic acetylcholine receptors 1 to 3 and 5 (M1R, M2R, M3R, and M5R, respectively), purified immunoglobulin (Ig) G fractions from patients with SjD (n = 10) and HCs (n = 10) were examined in Chinese hamster ovary (CHO) cells transfected with the specific receptor using calcium mobilisation and cyclic adenosine monophosphate (cAMP) accumulation assays.

RESULTS

IgG autoantibodies against M1R to M5R were significantly increased in patients with SjD compared with HCs (p ≤ .05) and detected in up to 30% of patients. A combination of anti-M2R, anti-M3R, and anti-M5R identified up to 31% of Ro/SSA-negative SjD cases, with 96% and 75% specificity for SjD vs HCs and SjD vs NSS, respectively. Functionally, purified IgG from SjD serum reduced calcium flux by up to 30% in M1R-, M3R-, and M5R-expressing CHO cells, whereas its effects on cAMP accumulation in M2R-transfected cells were absent.

CONCLUSIONS

The association between autoantibodies targeting M1R to M5R in patients with SjD and their functional quantification provides strong evidence that autoantibodies against all muscarinic receptor isotypes may have pathogenic relevance in SjD.