Humoral Immune Response in IBD Patients Three and Six Months after Vaccination with the SARS-CoV-2 mRNA Vaccines mRNA-1273 and BNT162b2.
Humoral Immune Response in IBD Patients Three and Six Months after Vaccination with the SARS-CoV-2 mRNA Vaccines mRNA-1273 and BNT162b2.
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DOI:
10.3390/biomedicines10010171
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发表时间:
2022-01-13
期刊:
影响因子:
4.7
通讯作者:
Nowacki TM
中科院分区:
文献类型:
--
作者:
Vollenberg R;Tepasse PR;Kühn JE;Hennies M;Strauss M;Rennebaum F;Schomacher T;Boeckel G;Lorentzen E;Bokemeyer A;Nowacki TM
Severe acute respiratory syndrome coronovirus-2 (SARS-CoV-2) is the cause of the coronavirus disease 2019 (COVID-19) pandemic. Vaccination is considered the core approach to containing the pandemic. There is currently insufficient evidence on the efficacy of these vaccines in immunosuppressed inflammatory bowel disease (IBD) patients. The aim of this study was to investigate the humoral response in immunosuppressed IBD patients after COVID-19 mRNA vaccination. In this prospective study, IgG antibody levels (AB) against the SARS-CoV-2 receptor-binding domain (spike-protein) were quantitatively determined. For assessing the potential neutralizing capacity, a SARS-CoV-2 surrogate neutralization test (sVNT) was employed in IBD patients (n = 95) and healthy controls (n = 38). Sera were examined prior to the first/second vaccination and 3/6 months after second vaccination. Patients showed lower sVNT (%) and IgG-S (AU/mL) AB both before the second vaccination (sVNT p < 0.001; AB p < 0.001) and 3 (sVNT p = 0.002; AB p = 0.001) and 6 months (sVNT p = 0.062; AB p = 0.061) after the second vaccination. Although seroconversion rates (sVNT, IgG-S) did not differ between the two groups 3 months after second vaccination, a significant difference was seen 6 months after second vaccination (sVNT p = 0.045). Before and three months after the second vaccination, patients treated with anti-tumor necrosis factor (TNF) agents showed significantly lower AB than healthy subjects. In conclusion, an early booster shot vaccination should be discussed for IBD patients on anti-TNF therapy.
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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
影响因子:
13.8
作者:
Nasserie T;Hittle M;Goodman SN
通讯作者:
Goodman SN
影响因子:
29.4
作者:
Pozdnyakova V;Botwin GJ;Sobhani K;Prostko J;Braun J;Mcgovern DPB;Melmed GY;Appel K;Banty A;Feldman E;Ha C;Kumar R;Lee S;Rabizadeh S;Stein T;Syal G;Targan S;Vasiliauskas E;Ziring D;Debbas P;Hampton M;Mengesha E;Stewart JL;Frias EC;Cheng S;Ebinger J;Figueiredo JC;Boland B;Charabaty A;Chiorean M;Cohen E;Flynn A;Valentine J;Fudman D;Horizon A;Hou J;Hwang C;Lazarev M;Lum D;Fausel R;Reddy S;Mattar M;Metwally M;Ostrov A;Parekh N;Raffals L;Sheibani S;Siegel C;Wolf D;Younes Z
通讯作者:
Younes Z
影响因子:
28.3
作者:
Gorbalenya, Alexander E.;Baker, Susan C.;Ziebuhr, John
通讯作者:
Ziebuhr, John
影响因子:
11.1
作者:
Deer RR;Rock MA;Vasilevsky N;Carmody L;Rando H;Anzalone AJ;Basson MD;Bennett TD;Bergquist T;Boudreau EA;Bramante CT;Byrd JB;Callahan TJ;Chan LE;Chu H;Chute CG;Coleman BD;Davis HE;Gagnier J;Greene CS;Hillegass WB;Kavuluru R;Kimble WD;Koraishy FM;Köhler S;Liang C;Liu F;Liu H;Madhira V;Madlock-Brown CR;Matentzoglu N;Mazzotti DR;McMurry JA;McNair DS;Moffitt RA;Monteith TS;Parker AM;Perry MA;Pfaff E;Reese JT;Saltz J;Schuff RA;Solomonides AE;Solway J;Spratt H;Stein GS;Sule AA;Topaloglu U;Vavougios GD;Wang L;Haendel MA;Robinson PN
通讯作者:
Robinson PN