False-positive detection of IgM anti-severe acute respiratory syndrome coronavirus 2 antibodies in patients with rheumatoid arthritis: Possible effects of IgM or IgG rheumatoid factors on immunochromatographic assay results

Author:

Oka Shomi12,Higuchi Takashi13,Furukawa Hiroshi12ORCID,Shimada Kota45,Hashimoto Atsushi46,Matsui Toshihiro24,Tohma Shigeto12

Affiliation:

1. Department of Rheumatology, National Hospital Organization Tokyo National Hospital, Kiyose, Japan

2. Clinical Research Center for Allergy and Rheumatology, National Hospital Organization Sagamihara National Hospital, Sagamihara, Japan

3. Department of Nephrology, Ushiku Aiwa General Hospital, Ushiku, Japan

4. Department of Rheumatology, National Hospital Organization Sagamihara National Hospital, Sagamihara, Japan

5. Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Fuchu, Japan

6. Department of Internal Medicine, Sagami Seikyou Hospital, Sagamihara, Japan

Abstract

Objectives: The severe acute respiratory syndrome coronavirus 2 causes coronavirus disease 2019. A serological test is conducted to determine prior infection by severe acute respiratory syndrome coronavirus 2. We investigated whether the results of anti-severe acute respiratory syndrome coronavirus 2 antibody tests are modified in patients with rheumatoid arthritis. Methods: Patients in Japan with rheumatoid arthritis were recruited at Sagamihara Hospital from July 2014 to October 2015 ( n = 38; 2014 cohort) and at Tokyo Hospital from June to October 2020 ( n = 93; 2020 cohort). Anti-severe acute respiratory syndrome coronavirus 2 antibodies were measured by electrochemiluminescence immunoassay or immunochromatographic assay. Results: Anti-severe acute respiratory syndrome coronavirus 2 antibodies were not detected in any of the samples from rheumatoid arthritis patients tested by electrochemiluminescence immunoassay. Anti-severe acute respiratory syndrome coronavirus 2 antibodies were detected by immunochromatographic assay in the 3 (7.9%) serum samples in the 2014 cohort and 15 (16.1%) serum samples in the 2020 cohort. The IgM rheumatoid factor levels were increased in rheumatoid arthritis patients with IgM anti-severe acute respiratory syndrome coronavirus 2 antibodies detected by immunochromatographic assay (mean ± standard deviation (IU/ml), 1223.0 ± 1308.7 versus 503.6 ± 1947.2; P = 0.0101). The levels of IgG rheumatoid factor were also upregulated in rheumatoid arthritis patients with IgM anti-severe acute respiratory syndrome coronavirus 2 antibodies detected by immunochromatographic assay (4.0 ± 0.7 versus 2.4 ± 0.9; P = 0.0013). Conclusion: The results of IgM anti-severe acute respiratory syndrome coronavirus 2 antibody testing by immunochromatographic assay are modified by IgM or IgG rheumatoid factors in rheumatoid arthritis patients.

Funder

National Hospital Organization

Eisai Co., Ltd.

Bristol-Myers Squibb Co.

Takeda Pharmaceutical Company

Merck Sharp and Dohme Inc.

Abbott Japan Co., Ltd.

Chugai Pharmaceutical Co., Ltd.

Teijin Pharma Limited

Astellas Pharma Inc.

Pfizer Japan Inc.

Mitsuibishi Tanabe Pharma Corporation

Publisher

SAGE Publications

Subject

General Medicine

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