Characterising the SARS-CoV-2 nucleocapsid (N) protein antibody response

被引:0
|
作者
Noble, C. C. A. [1 ,2 ]
Mcdonald, E. [2 ]
Nicholson, S. [3 ]
Biering-Sorensen, S. [2 ]
Pittet, L. F. [1 ,2 ,4 ,5 ]
Byrne, A. L. [6 ,7 ,8 ]
Croda, J. [9 ,10 ,11 ]
Dalcolmo, M. [12 ]
Lacerda, M. V. G. [13 ,14 ,15 ]
Lucas, M. [16 ,17 ,18 ,19 ]
Lynn, D. J. [20 ,21 ]
Aymerich, C. Prat [22 ,23 ]
Richmond, P. C. [19 ,24 ,25 ]
Warris, A. [26 ,27 ]
Curtis, N. [1 ,2 ,28 ]
Messina, N. L. [1 ,2 ]
机构
[1] Univ Melbourne, Dept Paediat, Parkville, Vic, Australia
[2] Murdoch Childrens Res Inst, Infect Dis Grp, 50 Flemington Rd, Parkville, Vic 3052, Australia
[3] Royal Melbourne Hosp, Peter Doherty Inst Infect & Immun, Victorian Infect Dis Reference Lab, Parkville, Vic, Australia
[4] Geneva Univ Hosp, Immunol Vaccinol Rheumatol & Infect Dis Unit, Geneva, Switzerland
[5] Fac Med, Geneva, Switzerland
[6] St Vincents Hosp Sydney, Darlinghurst, NSW, Australia
[7] Socios Salud, Partners Hlth, San Isidro, Peru
[8] Thorac Soc Australia & New Zealand, NSW ACT Branch, Chatswood, Australia
[9] Yale Sch Publ Hlth, Dept Epidemiol Microbial Dis, New Haven, CT USA
[10] Fundacao Oswaldo Cruz, Fiocruz Mato Grosso Do Sul, Campo Grande, Brazil
[11] Univ Fed Mato Grosso Do Sul, Campo Grande, Brazil
[12] ENSP FIOCRUZ, Ctr Referencia Prof Helio Fraga, Fundacao Oswaldo Cruz, Rio De Janeiro, Brazil
[13] Fundacao Med Trop Dr Heitor Vieira Dourado, Manaus, Brazil
[14] Fundacao Oswaldo Cruz, Inst Leonidas & Maria Deane, Minist Hlth, Manaus, Brazil
[15] Univ Texas Med Branch, Dermatol, Galveston, TX USA
[16] Queen Elizabeth II Med Ctr, Dept Immunol, Pathwest, Nedlands, WA, Australia
[17] Perth Childrens Hosp, Dept Immunol, Nedlands, WA, Australia
[18] Sir Charles Gairdner Hosp, Dept Immunol, Nedlands, WA, Australia
[19] Univ Western Australia, Sch Med, Perth, WA, Australia
[20] South Australian Hlth & Med Res Inst, Precis Med Theme, Adelaide, SA, Australia
[21] Flinders Univ S Australia, Flinders Hlth & Med Res Inst, Bedford Pk, SA, Australia
[22] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[23] European Clin Res Alliance Infect Dis, ECRAID, Utrecht, Netherlands
[24] Telethon Kids Inst, Wesfarmers Ctr Vaccines & Infect Dis, Nedlands, WA, Australia
[25] Perth Childrens Hosp, Dept Immunol & Gen Paediat, Nedlands, WA, Australia
[26] Univ Exeter, Med Res Council, Ctr Med Mycol, Exeter, England
[27] Great Ormond St Hosp Sick Children, Dept Infect Dis, London, England
[28] Royal Childrens Hosp Melbourne, Infect Dis, Parkville, Vic, Australia
基金
英国医学研究理事会; 瑞士国家科学基金会; 比尔及梅琳达.盖茨基金会;
关键词
SARS-CoV-2; COVID-19; Nucleocapsid protein; Antibody; Anti-N; Seroconversion; Vaccination; CoronaVac; VACCINE;
D O I
10.1016/j.jinf.2025.106436
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: SARS-CoV-2 nucleocapsid (N) protein antibodies can be used to identify the serological response to natural infection in those who have previously received a COVID-19 spike-based vaccine. Anti-N antibody responses can also be induced by inactivated whole SARS-CoV-2 virus vaccines, such as CoronaVac. We aimed to characterise antibody responses to the N protein following COVID-19 and following vaccination with CoronaVac. Methods: Using participants from an international randomised controlled trial, we investigated the evolution of anti-N antibody responses over time in two separate groups: adults following COVID-19, and in adults following vaccination with CoronaVac. Results: In 212 participants who had COVID-19, the anti-N seroconversion rate was 96.9% in those infected following an incomplete course of COVID-19 (spike-based) vaccinations and 88.2% in those infected following a complete course. Anti-N antibody indices were highly variable between participants, and higher in participants who had more severe COVID-19 symptoms, were aged >= 60 years, were unvaccinated, had comorbidities and those resident in Brazil. Most participants remained seropositive after 12 months. In 317 separate participants, the anti-N seroconversion rate was 63.5% following CoronaVac vaccination, with variable antibody indices. Conclusions: Anti-N responses to COVID-19 and CoronaVac are highly variable but persistent. A prior complete course of COVID-19 spike-based vaccination reduced both anti-N seroconversion and antibody indices following COVID-19. (c) 2025 The Author(s). Published by Elsevier Ltd on behalf of The British Infection Association. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:9
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