COVID-19 Vaccination in Multiple Sclerosis and Inflammatory Diseases: Effects from Disease-Modifying Therapy, Long-Term Seroprevalence and Breakthrough Infections.
COVID-19 Vaccination in Multiple Sclerosis and Inflammatory Diseases: Effects from Disease-Modifying Therapy, Long-Term Seroprevalence and Breakthrough Infections.
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DOI:
10.3390/vaccines10050695
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发表时间:
2022-04-28
期刊:
影响因子:
7.8
通讯作者:
Weinstock-Guttman, Bianca
中科院分区:
文献类型:
--
作者:
Jakimovski, Dejan;Zakalik, Karen;Awan, Samreen;Kavak, Katelyn S.;Pennington, Penny;Hojnacki, David;Kolb, Channa;Lizarraga, Alexis A.;Eckert, Svetlana P.;Sarrosa, Rosila;Vineetha, Kamath;Edwards, Keith;Weinstock-Guttman, Bianca
Background: To determine the effect of disease-modifying therapies (DMT) on humoral postvaccine seroconversion, long-term humoral response, and breakthrough COVID-19 infections in persons with multiple sclerosis (PwMS) and other neuroinflammatory disorders. Methods: A total of 757 PwMS and other neuroinflammatory disorders were recruited in two MS centers and vaccinated with one of the FDA-approved vaccines (BNT162b2, mRNA-1273, Ad26.COV2.S). The primary outcomes are the rate of humoral postvaccine seroconversion and anti-severe acute respiratory syndrome coronavirus 2 (anti-SARS-CoV-2) immunoglobulin G (IgG) differences between patients on different DMTs. Secondary measures include breakthrough infections and humoral response after six months. Other outcomes include differences in vaccine response between SARS-CoV-2 vaccines and the effects of age and comorbidities on the vaccine response. Results: A total of 465 (68.4%) PwMS and 55 (74.3%) patients with neuroinflammatory diseases were seropositive at 4–12 weeks after vaccination. A significant difference in seroconversion based on the DMT used at the time of vaccination (p < 0.001) was observed, with the lowest rates seen in patients treated with anti-CD20 antibodies (23.2%) and sphingosine-1-phosphate modulators (S1P) (30.8%). In seropositive patients, there was a significant decrease in anti-SARS IgG from mean 20.0 to 4.7 at six months (p = 0.004). Thirty-nine patients had breakthrough infection, but only two seronegative patients required hospitalization. mRNA vaccines resulted in significantly greater seroconversion compared to Ad26.COV2.S (p < 0.001). Older age and presence of cardiovascular comorbidities were associated with lower anti-SARS IgG (p = 0.021 and p = 0.003, respectively) Conclusions: PwMS and neuroinflammatory disorders treated with anti-CD20 and S1P medications have lower humoral response after anti-SARS-CoV-2 vaccination, even after booster dose. Waning of the humoral response puts vaccinated PwMS at a greater risk of COVID-19 breakthrough.
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影响因子:
11.1
作者:
Sormani MP;Inglese M;Schiavetti I;Carmisciano L;Laroni A;Lapucci C;Da Rin G;Serrati C;Gandoglia I;Tassinari T;Perego G;Brichetto G;Gazzola P;Mannironi A;Stromillo ML;Cordioli C;Landi D;Clerico M;Signoriello E;Frau J;Ferrò MT;Di Sapio A;Pasquali L;Ulivelli M;Marinelli F;Callari G;Iodice R;Liberatore G;Caleri F;Repice AM;Cordera S;Battaglia MA;Salvetti M;Franciotta D;Uccelli A;CovaXiMS study group on behalf of the Italian Covid-19 Alliance in MS
通讯作者:
CovaXiMS study group on behalf of the Italian Covid-19 Alliance in MS
影响因子:
4
作者:
Schiavetti I;Ponzano M;Signori A;Bovis F;Carmisciano L;Sormani MP
通讯作者:
Sormani MP
影响因子:
48
作者:
Thompson, Alan J.;Banwell, Brenda L.;Cohen, Jeffrey A.
通讯作者:
Cohen, Jeffrey A.
DOI:
10.1056/nejmoa2109072
发表时间:
2021-10-14
期刊:
The New England journal of medicine
影响因子:
--
作者:
Bergwerk M;Gonen T;Lustig Y;Amit S;Lipsitch M;Cohen C;Mandelboim M;Levin EG;Rubin C;Indenbaum V;Tal I;Zavitan M;Zuckerman N;Bar-Chaim A;Kreiss Y;Regev-Yochay G
通讯作者:
Regev-Yochay G
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