Longitudinal profile of immunoglobulin G (IgG), IgM, and TgA antibodies against the severe acute respiratory syndrome (SARS) coronavirus nucleocapsid protein in patients with pneumonia due to the SARS coronavirus

被引:130
作者
Woo, PCY
Lau, SKP
Wong, BHL
Chan, KH
Chu, CM
Tsoi, HW
Huang, Y
Peiris, JSM
Yuen, KY
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
[2] United Christian Hosp, Dept Med, Div Resp Med, Hong Kong, Hong Kong, Peoples R China
关键词
D O I
10.1128/CDLI.11.4.665-668.2004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
By using a recombinant severe acute respiratory syndrome coronavirus (SARS-CoV) nucleocapsid protein-based enzyme-linked immunosorbent assay (ELISA) and serum specimens serially collected (from day 0 to day 240 after symptom onset) from patients with pneumonia due to SARS-CoV, we analyzed the longitudinal profiles of immunoglobulin G (IgG), IgM, and IgA antibodies against the SARS-CoV nucleocapsid protein in patients with pneumonia due to SARS-CoV. For IgG, the median optical density at 450 nm (OD450) turned positive at day 17 and a biphasic response was observed. At day 240, all patients were still positive for anti-nucleocapsid protein IgG antibody. For IgM, the median OD450 turned positive at day 20.5, peaked at about day 80, and fell to below the baseline level at about day 180. At day 240, 36% of the patients were still positive for anti-nucleocapsid protein IgM antibody. For IgA, the median OD450 turned positive at day 17, peaked at about day 50, and fell to below the baseline level at about day 180. At day 240, 36% of the patients were still positive for anti-nucleocapsid protein IgA antibody. The time of seroconversion detected by the recombinant SARS-CoV nucleocapsid protein-based ELISA and that detected by indirect immunofluorescence assay were similar. The median times of seroconversion for IgG, IgM, and IgA detected by the indirect immunofluorescence assay were 17 days (17 days by ELISA), 16.5 days (20.5 days by ELISA), and 17.5 days (17 days by ELISA), respectively, after disease onset. One, four, and one of the six patients who died did not produce any IgG, IgM, and IgA antibodies against the nucleocapsid protein of SARS-CoV, respectively, although these antibodies were detected in all six patients by the indirect immunofluorescence assay. Further studies should be performed to see whether SARS-CoV nucleocapsid protein antibody positivity has any prognostic significance.
引用
收藏
页码:665 / 668
页数:4
相关论文
共 12 条
  • [1] ENZYME-LINKED-IMMUNOSORBENT-ASSAY FOR DETECTING ANTIBODIES TO BORNA-DISEASE VIRUS-SPECIFIC PROTEINS
    BRIESE, T
    HATALSKI, CG
    KLICHE, S
    PARK, YS
    LIPKIN, WI
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (02) : 348 - 351
  • [2] Detection of antibodies specific to an antigenic cell wall galactomannoprotein for serodiagnosis of Aspergillus fumigatus aspergillosis
    Chan, CM
    Woo, PCY
    Leung, ASP
    Lau, SKP
    Che, XY
    Cao, L
    Yuen, KY
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (06) : 2041 - 2045
  • [3] Isolation and characterization of viruses related to the SARS coronavirus from animals in Southern China
    Guan, Y
    Zheng, BJ
    He, YQ
    Liu, XL
    Zhuang, ZX
    Cheung, CL
    Luo, SW
    Li, PH
    Zhang, LJ
    Guan, YJ
    Butt, KM
    Wong, KL
    Chan, KW
    Lim, W
    Shortridge, KF
    Yuen, KY
    Peiris, JSM
    Poon, LLM
    [J]. SCIENCE, 2003, 302 (5643) : 276 - 278
  • [4] A novel coronavirus associated with severe acute respiratory syndrome
    Ksiazek, TG
    Erdman, D
    Goldsmith, CS
    Zaki, SR
    Peret, T
    Emery, S
    Tong, SX
    Urbani, C
    Comer, JA
    Lim, W
    Rollin, PE
    Dowell, SF
    Ling, AE
    Humphrey, CD
    Shieh, WJ
    Guarner, J
    Paddock, CD
    Rota, P
    Fields, B
    DeRisi, J
    Yang, JY
    Cox, N
    Hughes, JM
    LeDuc, JW
    Bellini, WJ
    Anderson, LJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (20) : 1953 - 1966
  • [5] Profile of specific antibodies to the SARS-associated coronavirus
    Li, G
    Chen, XJ
    Xu, AL
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (05) : 508 - 509
  • [6] Current concepts: The severe acute respiratory syndrome
    Peiris, JSM
    Yuen, KY
    Osterhaus, ADME
    Stohr, K
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (25) : 2431 - 2441
  • [7] Coronavirus as a possible cause of severe acute respiratory syndrome
    Peiris, JSM
    Lai, ST
    Poon, LLM
    Guan, Y
    Yam, LYC
    Lim, W
    Nicholls, J
    Yee, WKS
    Yan, WW
    Cheung, MT
    Cheng, VCC
    Chan, KH
    Tsang, DNC
    Yung, RWH
    Ng, TK
    Yuen, KY
    [J]. LANCET, 2003, 361 (9366) : 1319 - 1325
  • [8] Clinical progression and viral load in a community outbreak of coronavirus-associated SARS pneumonia: a prospective study
    Peiris, JSM
    Chu, CM
    Cheng, VCC
    Chan, KS
    Hung, IFN
    Poon, LLM
    Law, KI
    Tang, BSF
    Hon, TYW
    Chan, CS
    Chan, KH
    Ng, JSC
    Zheng, BJ
    Ng, WL
    Lai, RWM
    Guan, Y
    Yuen, KY
    [J]. LANCET, 2003, 361 (9371) : 1767 - 1772
  • [9] Detection of specific antibodies to severe acute respiratory syndrome (SARS) coronavirus nucleocapsid protein for serodiagnosis of SARS coronavirus pneumonia
    Woo, PCY
    Lau, SKP
    Wong, BHL
    Tsoi, H
    Fung, AMY
    Chan, KH
    Tam, VKP
    Peiris, JSM
    Yuen, K
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (05) : 2306 - 2309
  • [10] Relative rates of non-pneumonic SARS coronavirus infection and SARS coronavirus pneumonia
    Woo, PCY
    Lau, SKP
    Tsoi, HW
    Chan, KH
    Wong, BHL
    Che, XY
    Tam, VKP
    Tam, SCF
    Cheng, VCC
    Hung, IFN
    Wong, SSY
    Zheng, BJ
    Guan, Y
    Yuen, KY
    [J]. LANCET, 2004, 363 (9412) : 841 - 845