Impaired Antibody Response to the BNT162b2 Messenger RNA Coronavirus Disease 2019 Vaccine in Patients With Systemic Lupus Erythematosus and Rheumatoid Arthritis.
Impaired Antibody Response to the BNT162b2 Messenger RNA Coronavirus Disease 2019 Vaccine in Patients With Systemic Lupus Erythematosus and Rheumatoid Arthritis.
复制标题
DOI:
10.1002/acr2.11299
复制
发表时间:
2021-09
影响因子:
3.4
通讯作者:
Troldborg A
中科院分区:
文献类型:
--
作者:
Ammitzbøll C;Bartels LE;Bøgh Andersen J;Risbøl Vils S;Elbaek Mistegård C;Dahl Johannsen A;From Hermansen ML;Kragh Thomsen M;Erikstrup C;Hauge EM;Troldborg A
With a vaccine effectiveness of 95% for preventing coronavirus disease 2019 (COVID‐19), Pfizer‐BioNTech BNT162b2 (BNT162b2) was the first vaccine against severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) to be approved. However, immunosuppressive therapy was an exclusion criterion in the phase 3 trial that led to approval. Thus, extrapolation of the trial results to patients with rheumatic diseases treated with immunosuppressive drugs warrants caution. Patients with systemic lupus erythematosus (SLE; n = 61) and rheumatoid arthritis (RA; n = 73) were included from the COPANARD (Corona Pandemic Autoimmune Rheumatic Disease) cohort, followed since the beginning of the COVID‐19 pandemic. Patients received the BNT162b2 vaccine between December 2020 and April 2021. All patients had total antibodies against SARS‐CoV‐2 measured before vaccination and 1 week after the second vaccination (VITROS Immunodiagnostic Products). Of 134 patients (median age, 70 years), 77% were able to mount a detectable serological response to the vaccine. Among patients treated with rituximab, only 24% had detectable anti–SARS‐CoV‐2 antibodies in their serum after vaccination. The time since the last rituximab treatment did not seem to influence the vaccine response. No significant difference was observed between patients with RA or SLE when adjusting for treatment, and no correlation between antibody levels and age was detected (r = −0.12; P = 0.18). Antibody measurements against SARS‐CoV‐2 in patients with RA and SLE after two doses of the BNT162b2 vaccine demonstrated that 23% of patients could not mount a detectable serological response to the vaccine. B cell–depleting therapy (BCDT) is of specific concern, and our findings call for particular attention to the patients receiving BCDT.
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
影响因子:
82.9
作者:
Ebinger JE;Fert-Bober J;Printsev I;Wu M;Sun N;Prostko JC;Frias EC;Stewart JL;Van Eyk JE;Braun JG;Cheng S;Sobhani K
通讯作者:
Sobhani K
影响因子:
27.4
作者:
Park, Jin Kyun;Lee, Yun Jong;Lee, Eun Bong
通讯作者:
Lee, Eun Bong
影响因子:
6.2
作者:
Marques CDL;Kakehasi AM;Pinheiro MM;Mota LMH;Albuquerque CP;Silva CR;Santos GPJ;Reis-Neto ET;Matos P;Devide G;Dantas A;Giorgi RD;Marinho AO;Valadares LDA;Melo AKG;Ribeiro FM;Ferreira GA;Santos FPS;Ribeiro SLE;Andrade NPB;Yazbek MA;Souza VA;Paiva ES;Azevedo VF;Freitas ABSB;Provenza JR;Toledo RA;Fontenelle S;Carneiro S;Xavier R;Pileggi GCS;Reis APMG
通讯作者:
Reis APMG
影响因子:
3.9
作者:
Bachiller-Corral, Javier;Boteanu, Alina;Vazquez-Diaz, Monica
通讯作者:
Vazquez-Diaz, Monica