Vaccine-induced seroconversion in participants in the North Carolina COVID-19 community Research Partnership.
Vaccine-induced seroconversion in participants in the North Carolina COVID-19 community Research Partnership.
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DOI:
10.1016/j.vaccine.2022.09.021
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发表时间:
2022-10-06
期刊:
影响因子:
5.5
通讯作者:
Berry, Andrea A.
中科院分区:
文献类型:
--
作者:
Friedman-Klabanoff, Deanna J.;Tjaden, Ashley H.;Santacatterina, Michele;Munawar, Iqra;Sanders, John W.;Herrington, David M.;Wierzba, Thomas F.;Berry, Andrea A.
Well-regulated clinical trials have shown FDA-approved COVID-19 vaccines to be immunogenic and highly efficacious. We evaluated seroconversion rates in adults reporting ≥ 1 dose of an mRNA COVID-19 vaccine in a cohort study of nearly 8000 adults residing in North Carolina to validate immunogenicity using a novel approach: at-home, participant administered point-of-care testing. Overall, 91.4% had documented seroconversion within 75 days of first vaccination (median: 31 days). Participants who were older and male participants were less likely to seroconvert (adults aged 41–65: adjusted hazard ratio [aHR] 0.69 [95% confidence interval (CI): 0.64, 0.73], adults aged 66–95: aHR 0.55 [95% CI: 0.50, 0.60], compared to those 18–40; males: aHR 0.92 [95% CI: 0.87, 0.98], compared to females). Participants with evidence of prior infection were more likely to seroconvert than those without (aHR 1.50 [95% CI: 1.19, 1.88]) and those receiving BNT162b2 were less likely to seroconvert compared to those receiving mRNA-1273 (aHR 0.84 [95% CI: 0.79, 0.90]). Reporting at least one new symptom after first vaccination did not affect time to seroconversion, but participants reporting at least one new symptom after second vaccination were more likely to seroconvert (aHR 1.11 [95% CI: 1.05, 1.17]). This data demonstrates the high community-level immunogenicity of COVID-19 vaccines, albeit with notable differences in older adults, and feasibility of using at-home, participant administered point-of-care testing for community cohort monitoring. Trial registration: ClinicalTrials.gov NCT04342884.
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影响因子:
5.5
作者:
Shachor-Meyouhas Y;Hussein K;Szwarcwort-Cohen M;Weissman A;Mekel M;Dabaja-Younis H;Hyams G;Horowitz NA;Kaplan M;Halberthal M
通讯作者:
Halberthal M
影响因子:
5.5
作者:
Tani N;Chong Y;Kurata Y;Gondo K;Oishi R;Goto T;Minami J;Onozawa K;Nagano S;Shimono N;Ikematsu H;Kuwano H
通讯作者:
Kuwano H
DOI:
10.2807/1560-7917.es.2021.26.6.2100096
发表时间:
2021-03
期刊:
Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin
影响因子:
--
作者:
Abu Jabal K;Ben-Amram H;Beiruti K;Batheesh Y;Sussan C;Zarka S;Edelstein M
通讯作者:
Edelstein M
DOI:
10.1093/infdis/jiab314
发表时间:
2021-09-01
期刊:
The Journal of infectious diseases
影响因子:
--
作者:
Demonbreun AR;Sancilio A;Velez ME;Ryan DT;Pesce L;Saber R;Vaught LA;Reiser NL;Hsieh RR;D'Aquila RT;Mustanski B;McDade TW;McNally EM
通讯作者:
McNally EM
DOI:
10.1056/nejmoa2027906
发表时间:
2020-12-17
期刊:
The New England journal of medicine
影响因子:
--
作者:
Walsh EE;Frenck RW Jr;Falsey AR;Kitchin N;Absalon J;Gurtman A;Lockhart S;Neuzil K;Mulligan MJ;Bailey R;Swanson KA;Li P;Koury K;Kalina W;Cooper D;Fontes-Garfias C;Shi PY;Türeci Ö;Tompkins KR;Lyke KE;Raabe V;Dormitzer PR;Jansen KU;Şahin U;Gruber WC
通讯作者:
Gruber WC