Detection of Anti-SARS-CoV-2 Nucleocapsid and Spike Antibodies in Patients with Coronavirus Disease 2019 in Japan

Author:

Furukawa Hiroshi1ORCID,Oka Shomi1,Higuchi Takashi12,Yamaguchi Miho3,Uchiyama Shota3,Koiwa Tomohiro3,Nakama Moriyuki4,Minegishi Masaaki4,Nagai Hideaki3,Tohma Shigeto1

Affiliation:

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

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

3. Department of Respiratory Medicine, National Hospital Organization Tokyo National Hospital, Kiyose, Japan

4. Department of Clinical Laboratory, National Hospital Organization Tokyo National Hospital, Kiyose, Japan

Abstract

OBJECTIVES Coronavirus Disease 2019 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Serological testing for anti-SARS-CoV-2 nucleocapsid (N) antibodies (Abs) and anti-SARS-CoV-2 spike (S) Abs is performed to detect prior COVID-19 infection. It is still controversial which antibodies are the most sensitive and specific, and which can be detected earliest after infection. Here, we evaluated the results of serological tests of anti-SARS-CoV-2 N and S Abs in Japan. METHODS Symptomatic COVID-19 patients (n = 84) and control patients with rheumatoid arthritis (n = 93) were recruited at Tokyo National Hospital. Anti-SARS-CoV-2 N and S Abs were measured by commercial electrochemiluminescence immunoassays. RESULTS The fraction of patients positive for anti-SARS-CoV-2 N and S Abs was highest >14 days after symptom onset. The frequency of anti-SARS-CoV-2 S Ab positivity at this time (80.4%) tended to be slightly but not significantly lower than anti-SARS-CoV-2 N Ab positivity (84.8%). Optimized cut-off levels for anti-SARS-CoV-2 N and S Ab positivity were lower than the manufacturer's recommended cut-off levels. Using multiple linear regression analyzes with anti-SARS-CoV-2 N and S Abs, we created an Ab-index with high sensitivity. CONCLUSION To increase the sensitivity of serological diagnostic tests for COVID-19, it is suggested that both anti-SARS-CoV-2 N and S Abs should be measured and cut-off levels decreased.

Funder

Teijin Pharma Limited

Abbott Japan Co., Ltd.

Astellas Pharma Inc.

Merck Sharp and Dohme Inc.

Pfizer Japan Inc.

Takeda Pharmaceutical Company

Bristol-Myers Squibb Co.

Chugai Pharmaceutical Co., Ltd.

Eisai Co., Ltd.

Mitsubishi Tanabe Pharma Corporation

National Hospital Organization

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine

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