Open AccessLow prevalence of antibodies to glucose‐6‐phosphate isomerase in patients with rheumatoid arthritis and a spectrum of other chronic autoimmune disorders
Author(s) -
Matsumoto Isao,
Lee David M.,
GoldbachMansky Raphaela,
Sumida Takayuki,
Hitchon Carol A.,
Schur Peter H.,
Anderson Ronald J.,
Coblyn Jonathan S.,
Weinblatt Michael E.,
Brenner Michael,
Duclos Bernard,
Pasquali JeanLouis,
ElGabalawy Hani,
Mathis Diane,
Benoist Christophe
Publication year - 2003
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.10898
Subject(s) - medicine , rheumatoid arthritis , antibody , arthritis , immunology , autoantibody , titer , autoimmune disease , psoriatic arthritis , population , antibody titer , environmental health
Objective Arthritis in the K/BxN mouse model results from pathogenic immunoglobulins that recognize glucose‐6‐phosphate isomerase (GPI), a glycolytic enzyme residing in the cytoplasm of all cells. Antibodies directed against GPI can, alone, transfer arthritis to healthy recipients. Previous experiments have revealed significant titers of anti‐GPI antibodies in the serum of many patients with rheumatoid arthritis (RA). We evaluated the generality of these observations in cohorts of patients with 12 different arthritic and chronic autoimmune diseases and in population‐matched healthy control subjects. Methods Anti‐GPI antibodies were assayed in 811 individual serum samples by enzyme‐linked immunosorbent assay with 2 forms of GPI, recombinant and native. Results were confirmed by immunoblotting. Results Several patients had significantly elevated anti‐GPI antibody titers, but without the prevalence or the specificity reported previously. Only 15% of RA patients had anti‐GPI antibodies (range 12–29% in different cohorts), with a higher prevalence in patients with active disease. Psoriatic arthritis, undifferentiated arthritis, and spondylarthropathy patients also displayed anti‐GPI antibodies at similar frequencies (12–25%). Similar titers were detected in a proportion (5–10%) of control subjects or patients with Crohn's disease or sarcoidosis. Very high titers were found in rare cases of RA and systemic lupus erythematosus. Conclusion No disease‐specific pattern of antibody positivity to GPI was apparent. While the antibody‐mediated mechanism at play in the mouse model may exemplify a generic mechanism for some forms of arthritis in humans, GPI itself does not appear to be a target common to the majority of RA patients.