Trajectory of IgG to SARS-CoV-2 After Vaccination With BNT162b2 or mRNA-1273 in an Employee Cohort and Comparison With Natural Infection.
Trajectory of IgG to SARS-CoV-2 After Vaccination With BNT162b2 or mRNA-1273 in an Employee Cohort and Comparison With Natural Infection.
复制标题
DOI:
10.3389/fimmu.2022.850987
复制
发表时间:
2022
影响因子:
7.3
通讯作者:
Wilson JM
中科院分区:
文献类型:
--
作者:
Keshavarz B;Richards NE;Workman LJ;Patel J;Muehling LM;Canderan G;Murphy DD;Brovero SG;Ailsworth SM;Eschenbacher WH;McGowan EC;Mann BJ;Nelson MR;Kadl A;Woodfolk JA;Platts-Mills TAE;Wilson JM
Three COVID-19 vaccines have received FDA-authorization and are in use in the United States, but there is limited head-to-head data on the durability of the immune response elicited by these vaccines. Using a quantitative assay we studied binding IgG antibodies elicited by BNT162b2, mRNA-1273 or Ad26.COV2.S in an employee cohort over a span out to 10 months. Age and sex were explored as response modifiers. Of 234 subjects in the vaccine cohort, 114 received BNT162b2, 114 received mRNA-1273 and six received Ad26.COV2.S. IgG levels measured between seven to 20 days after the second vaccination were similar in recipients of BNT162b2 and mRNA-127 and were ~50-fold higher than in recipients of Ad26.COV2.S. However, by day 21 and at later time points IgG levels elicited by BNT162b2 were lower than mRNA-1273. Accordingly, the IgG decay curve was steeper for BNT162b2 than mRNA-1273. Age was a significant modifier of IgG levels in recipients of BNT162b2, but not mRNA-1273. After six months, IgG levels elicited by BNT162b2, but not mRNA-1273, were lower than IgG levels in patients who had been hospitalized with COVID-19 six months earlier. Similar findings were observed when comparing vaccine-elicited antibodies with steady-state IgG targeting seasonal human coronaviruses. Differential IgG decay could contribute to differences observed in clinical protection over time between BNT162b2 and mRNA-1273.
登录
查看更多内容
DOI:
10.1056/nejmoa2034577
发表时间:
2020-12-31
期刊:
The New England journal of medicine
影响因子:
--
作者:
Polack FP;Thomas SJ;Kitchin N;Absalon J;Gurtman A;Lockhart S;Perez JL;Pérez Marc G;Moreira ED;Zerbini C;Bailey R;Swanson KA;Roychoudhury S;Koury K;Li P;Kalina WV;Cooper D;Frenck RW Jr;Hammitt LL;Türeci Ö;Nell H;Schaefer A;Ünal S;Tresnan DB;Mather S;Dormitzer PR;Şahin U;Jansen KU;Gruber WC;C4591001 Clinical Trial Group
通讯作者:
C4591001 Clinical Trial Group
DOI:
10.1016/s2213-2600(21)00407-0
发表时间:
2021-12
期刊:
The Lancet. Respiratory medicine
影响因子:
--
作者:
Milne G;Hames T;Scotton C;Gent N;Johnsen A;Anderson RM;Ward T
通讯作者:
Ward T
DOI:
10.1093/infdis/jiab593
发表时间:
2022-04-01
期刊:
The Journal of infectious diseases
影响因子:
--
作者:
Naranbhai V;Garcia-Beltran WF;Chang CC;Berrios Mairena C;Thierauf JC;Kirkpatrick G;Onozato ML;Cheng J;St Denis KJ;Lam EC;Kaseke C;Tano-Menka R;Yang D;Pavlovic M;Yang W;Kui A;Miller TE;Astudillo MG;Cahill JE;Dighe AS;Gregory DJ;Poznansky MC;Gaiha GD;Balazs AB;Iafrate AJ
通讯作者:
Iafrate AJ
DOI:
10.15585/mmwr.mm7038e1
发表时间:
2021-09-24
期刊:
MMWR. Morbidity and mortality weekly report
影响因子:
--
作者:
Self WH;Tenforde MW;Rhoads JP;Gaglani M;Ginde AA;Douin DJ;Olson SM;Talbot HK;Casey JD;Mohr NM;Zepeski A;McNeal T;Ghamande S;Gibbs KW;Files DC;Hager DN;Shehu A;Prekker ME;Erickson HL;Gong MN;Mohamed A;Henning DJ;Steingrub JS;Peltan ID;Brown SM;Martin ET;Monto AS;Khan A;Hough CL;Busse LW;Ten Lohuis CC;Duggal A;Wilson JG;Gordon AJ;Qadir N;Chang SY;Mallow C;Rivas C;Babcock HM;Kwon JH;Exline MC;Halasa N;Chappell JD;Lauring AS;Grijalva CG;Rice TW;Jones ID;Stubblefield WB;Baughman A;Womack KN;Lindsell CJ;Hart KW;Zhu Y;Mills L;Lester SN;Stumpf MM;Naioti EA;Kobayashi M;Verani JR;Thornburg NJ;Patel MM;IVY Network
通讯作者:
IVY Network
影响因子:
120.7
作者:
Stephenson, Kathryn E.;Le Gars, Mathieu;Barouch, Dan H.
通讯作者:
Barouch, Dan H.