Circulating antibodies against rat parotid gland M3 muscarinic receptors in primary Sjögren's syndrome

• Published in: Clinical and experimental immunology 1996-06, Vol.104 (3), p.454-459
• Main Authors: Bacman, S., Sterin‐Borda, L., JosÉ Camusso, J., Arana, R., Hubscher, O., Borda, E.
• Format: Article
• Language: English
• Subjects: Adolescent; Adrenergic beta-Agonists - pharmacology; Adult; Animals; antibodies; Antibodies, Blocking - immunology; Atropine - pharmacology; Biological and medical sciences; Carbachol - pharmacology; Carbamates - pharmacology; Cyclic AMP - metabolism; Cyclic GMP - metabolism; Dose-Response Relationship, Drug; Female; Humans; Immunoglobulin G - analysis; Immunoglobulin G - immunology; Isoproterenol - pharmacology; Medical sciences; Muscarinic Antagonists - immunology; Muscarinic Antagonists - pharmacology; muscarinic receptors; Original; Parasympatholytics - pharmacology; parotid gland; Parotid Gland - immunology; Phenylcarbamates; Phosphatidylinositols - metabolism; Piperidines - pharmacology; Pirenzepine - analogs & derivatives; Pirenzepine - pharmacology; primary Sjögren's syndrome; Protease Inhibitors - pharmacology; Quinuclidinyl Benzilate - immunology; Rats; Rats, Wistar; Receptors, Muscarinic - immunology; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis; Sjogren's Syndrome - blood; Sjogren's Syndrome - immunology
• ISSN: 0009-9104; 1365-2249
• DOI: 10.1046/j.1365-2249.1996.42748.x

In this study we demonstrate that IgG present in the sera of patients with primary Sjögren's syndrome (PSS) could bind and activate muscarinic acetylcholine receptors (mAChRs) of rat parotid gland. These antibodies were able to inhibit in a non‐competitive manner the binding of 3H‐quinuclidinyl benzilate (QNB) to  mAChRs of purified rat parotid gland membranes. Moreover, IgG from PSS could modify biological effects mediated by  mAChR activation; i.e. decrease cAMP, increase phosphoinositide turnover without affecting cGMP. Atropine and 4‐DAMP blocked all of these effects, and carbachol mimicked them, confirming the M3 subtype  mAChRs mediated PSS IgG action. Neither binding nor biological effect were obtained with IgG from sera of normal women. The prevalence of cholinergic antibody was 100% in PSS, and was independent of Ro/SS‐A and La/SS‐B antibodies. It could be concluded that antibody against  mAChRs may be another serum factor to be considered in the pathophysiology of the development of PSS.