Ko Jae-Hoon, Joo Eun-Jeong, Park Su-Jin, Baek Jin Yang, Kim Won Duk, Jee Jaehwan, Kim Chul Joong, Jeong Chul, Kim Yae-Jean, Shon Hye Jin, Kang Eun-Suk, Choi Young Ki, Peck Kyong Ran
Division of Infectious Diseases, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul 06351, Korea.
Division of Infectious Diseases, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 03181, Korea.
J Clin Med. 2020 Jul 17;9(7):2268. doi: 10.3390/jcm9072268.
To investigate antibody production in asymptomatic and mild COVID-19 patients.
Sera from asymptomatic to severe COVID-19 patients were collected. Microneutralization (MN), fluorescence immunoassay (FIA), and enzyme-linked immunosorbent assay (ELISA) were performed.
A total of 70 laboratory-confirmed COVID-19 patients were evaluated, including 15 asymptomatic/anosmia, 49 mild symptomatic, and 6 pneumonia patients. The production of the neutralizing antibody was observed in 100% of pneumonia, 93.9% of mild symptomatic, and 80.0% of asymptomatic/anosmia groups. All the patients in the pneumonia group showed high MN titer (≥1:80), while 36.7% of mild symptomatic and 20.0% of asymptomatic/anosmia groups showed high titer ( < 0.001). Anti-SARS-CoV-2 antibodies could be more sensitively detected by FIA IgG (98.8%) and ELISA (97.6%) in overall. For the FIA IgG test, all patients in the pneumonia group exhibited a high COI value (≥15.0), while 89.8% of mild symptomatic and 73.3% of asymptomatic/anosmia groups showed a high value ( = 0.049). For the ELISA test, all patients in the pneumonia group showed a high optical density (OD) ratio (≥3.0), while 65.3% of mild symptomatic and 53.3% of asymptomatic/anosmia groups showed a high ratio ( = 0.006).
Most asymptomatic and mild COVID-19 patients produced the neutralizing antibody, although the titers were lower than pneumonia patients. ELISA and FIA sensitively detected anti-SARS-CoV-2 antibodies.
研究无症状和轻症新冠患者的抗体产生情况。
收集从无症状到重症新冠患者的血清。进行了微量中和试验(MN)、荧光免疫分析(FIA)和酶联免疫吸附测定(ELISA)。
共评估了70例实验室确诊的新冠患者,包括15例无症状/嗅觉丧失患者、49例轻症患者和6例肺炎患者。在100%的肺炎患者、93.9%的轻症患者和80.0%的无症状/嗅觉丧失患者组中观察到中和抗体的产生。肺炎组所有患者的MN滴度均较高(≥1:80),而轻症组36.7%和无症状/嗅觉丧失组20.0%的患者滴度较高(<0.001)。总体而言,FIA IgG(98.8%)和ELISA(97.6%)能更灵敏地检测出抗SARS-CoV-2抗体。对于FIA IgG检测,肺炎组所有患者的COI值均较高(≥15.0),而轻症组89.8%和无症状/嗅觉丧失组73.3%的患者COI值较高(P = 0.049)。对于ELISA检测,肺炎组所有患者的光密度(OD)比值均较高(≥3.0),而轻症组65.3%和无症状/嗅觉丧失组53.3%的患者OD比值较高(P = 0.006)。
大多数无症状和轻症新冠患者产生了中和抗体,尽管其滴度低于肺炎患者。ELISA和FIA能灵敏地检测出抗SARS-CoV-2抗体。