Hiki Makoto, Tabe Yoko, Ai Tomohiko, Matsue Yuya, Harada Norihiro, Sugimoto Kiichi, Matsushita Yasushi, Matsushita Masakazu, Wakita Mitsuru, Misawa Shigeki, Idei Mayumi, Miida Takashi, Tamura Naoto, Takahashi Kazuhisa, Naito Toshio
Department of Emergency Medicine, Juntendo University Faculty of Medicine, Tokyo, Japan.
Department of Cardiovascular Biology and Medicine, Juntendo University Faculty of Medicine, Tokyo, Japan.
PLoS One. 2021 Apr 6;16(4):e0249449. doi: 10.1371/journal.pone.0249449. eCollection 2021.
To determine the seroprevalence of anti-SARS-CoV-2 IgG and IgM antibodies in symptomatic Japanese COVID-19 patients.
Serum samples (n = 114) from 34 COVID-19 patients with mild to critical clinical manifestations were examined. The presence and titers of IgG antibody for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) were determined by a chemiluminescent microparticle immunoassay (CMIA) using Alinity i SARS-CoV-2 IgG and by an immunochromatographic (IC) IgM/IgG antibody assay using the Anti-SARS-CoV-2 Rapid Test.
IgG was detected by the CMIA in 40%, 88%, and 100% of samples collected within 1 week, 1-2 weeks, and 2 weeks after symptom onset in severe and critical cases, and 0%, 38%, and 100% in mild/moderate cases, respectively. In severe and critical cases, the positive IgG detection rate with the IC assay was 60% within one week and 63% between one and two weeks. In mild/moderate cases, the positive IgG rate was 17% within one week and 63% between one and two weeks; IgM was positive in 80% and 75% of severe and critical cases, and 42% and 88% of mild/moderate cases, respectively. On the CMIA, no anti-SARS-CoV-2 IgG antibodies were detected in COVID-19 outpatients with mild symptoms within 10 days from onset, whereas 50% of samples from severe inpatients were IgG-positive in the same period. The IC assay detected higher IgM positivity earlier from symptom onset in severe and critical cases than in mild/moderate cases.
A serologic anti-SARS-CoV-2 antibody analysis can complement PCR for diagnosing COVID-19 14 days after symptom onset.
确定有症状的日本新冠肺炎患者中抗SARS-CoV-2 IgG和IgM抗体的血清阳性率。
检测了34例有轻至重症临床表现的新冠肺炎患者的血清样本(n = 114)。采用Alinity i SARS-CoV-2 IgG化学发光微粒子免疫分析(CMIA)和抗SARS-CoV-2快速检测免疫层析(IC)IgM/IgG抗体检测法,测定严重急性呼吸综合征冠状病毒2(SARS-CoV-2)IgG抗体的存在情况和滴度。
在重症和危重症病例中,症状出现后1周内、1 - 2周和2周内采集的样本中,CMIA检测到IgG的比例分别为40%、88%和100%,在轻/中症病例中分别为0%、38%和100%。在重症和危重症病例中,IC检测法在1周内IgG阳性检出率为60%,1至2周内为63%。在轻/中症病例中,1周内IgG阳性率为17%,1至2周内为63%;IgM在重症和危重症病例中的阳性率分别为80%和75%,在轻/中症病例中分别为42%和88%。CMIA检测显示,症状出现10天内的轻症新冠肺炎门诊患者未检测到抗SARS-CoV-2 IgG抗体,而同期重症住院患者样本中有50%为IgG阳性。IC检测法在重症和危重症病例中比轻/中症病例更早从症状出现时检测到更高的IgM阳性率。
症状出现14天后,血清学抗SARS-CoV-2抗体分析可作为诊断新冠肺炎的PCR检测的补充。