Antibody Responses after SARS-CoV-2 Vaccination in Patients with Liver Diseases.
Antibody Responses after SARS-CoV-2 Vaccination in Patients with Liver Diseases.
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DOI:
10.3390/v14020207
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发表时间:
2022-01-21
期刊:
影响因子:
--
通讯作者:
Androutsakos T
中科院分区:
文献类型:
--
作者:
Bakasis AD;Bitzogli K;Mouziouras D;Pouliakis A;Roumpoutsou M;Goules AV;Androutsakos T
The novel mRNA-based vaccines against SARS-CoV-2 display encouraging safety and efficacy profiles. However, there is a paucity of data regarding their immunogenicity and safety in patients with liver diseases (PWLD), especially in those with cirrhosis. We prospectively assessed anti-SARS-CoV-2 S-spike IgG antibodies and neutralizing activity in fully vaccinated PWLD (n = 87) and controls (n = 40). Seroconversion rates were 97.4% (37/38) in cirrhotic PWLD, 87.8% (43/49) in non-cirrhotic PWLD and 100% (40/40) in controls. Adequate neutralizing activity was detected in 92.1% (35/38), 87.8% (43/49) and 100% (40/40) of cirrhotics, non-cirrhotics and controls, respectively. On multivariable analysis, immunosuppressive treatment was negatively correlated with anti-SARS-CoV-2 antibody titers (coefficient (SE): −2.716 (0.634), p < 0.001) and neutralizing activity (coefficient (SE): −24.379 (4.582), p < 0.001), while age was negatively correlated only with neutralizing activity (coefficient (SE): −0.31(0.14), p = 0.028). A total of 52 responder PWLD were reassessed approximately 3 months post-vaccination and no differences were detected in humoral responses between cirrhotic and non-cirrhotic PWLD. No significant side effects were noted post vaccination, while no symptomatic breakthrough infections were reported during a 6-month follow up. Overall, our study shows that m-RNA-based SARS-CoV-2 vaccines are safe and efficacious in PWLD. However, PWLD under immunosuppressive treatment and those of advanced age should probably be more closely monitored after vaccination.
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影响因子:
27.4
作者:
Haberman RH;Herati R;Simon D;Samanovic M;Blank RB;Tuen M;Koralov SB;Atreya R;Tascilar K;Allen JR;Castillo R;Cornelius AR;Rackoff P;Solomon G;Adhikari S;Azar N;Rosenthal P;Izmirly P;Samuels J;Golden B;Reddy SM;Neurath MF;Abramson SB;Schett G;Mulligan MJ;Scher JU
通讯作者:
Scher JU
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:
7.8
作者:
Ferrari D;Clementi N;Criscuolo E;Ambrosi A;Corea F;Di Resta C;Tomaiuolo R;Mancini N;Locatelli M;Plebani M;Banfi G
通讯作者:
Banfi G
影响因子:
25.7
作者:
Rabinowich L;Grupper A;Baruch R;Ben-Yehoyada M;Halperin T;Turner D;Katchman E;Levi S;Houri I;Lubezky N;Shibolet O;Katchman H
通讯作者:
Katchman H
影响因子:
6.4
作者:
McCashland, TM;Preheim, LC;Gentry-Nielsen, MJ
通讯作者:
Gentry-Nielsen, MJ