Artigo Acesso aberto Produção Nacional Revisado por pares

Immunogenicity, safety, and antiphospholipid antibodies after SARS-CoV-2 vaccine in patients with primary antiphospholipid syndrome

2022; SAGE Publishing; Volume: 31; Issue: 8 Linguagem: Inglês

10.1177/09612033221102073

ISSN

1477-0962

Autores

Flávio Signorelli, Gustavo Guimarães Moreira Balbi, Nádia Emi Aikawa, Clóvis A. Silva, Léonard de Vinci Kanda Kupa, Ana Cristina de Medeiros Ribeiro, Emily Figueiredo Neves Yuki, Sandra Gofinet Pasoto, Carla GS Saad, Eduardo Ferreira Borba, Luciana Parente Costa Seguro, Tatiana do Nascimento Pedrosa, Vitor Antônio de Angeli Oliveira, Ana Luisa Cerqueira de Sant’Ana Costa, Carolina Torres Ribeiro, Roseli Eliana Beseggio Santos, Danieli Andrade, Eloísa Bonfá,

Tópico(s)

SARS-CoV-2 and COVID-19 Research

Resumo

Coronavirus disease 19 (COVID-19) has an increased risk of coagulopathy with high frequency of antiphospholipid antibodies (aPL). Recent reports of thrombosis associated with adenovirus-based vaccines raised concern that SARS-CoV-2 immunization in primary antiphospholipid syndrome (PAPS) patients may trigger clotting complications. Our objectives were to assess immunogenicity, safety, and aPL production in PAPS patients, after vaccinating with Sinovac-CoronaVac, an inactivated virus vaccine against COVID-19.This prospective controlled phase-4 study of PAPS patients and a control group (CG) consisted of a two-dose Sinovac-CoronaVac (D0/D28) and blood collection before vaccination (D0), at D28 and 6 weeks after second dose (D69) for immunogenicity/aPL levels. Outcomes were seroconversion (SC) rates of anti-SARS-CoV-2 S1/S2 IgG and/or neutralizing antibodies (NAb) at D28/D69 in naïve participants. Safety and aPL production were also assessed.We included 44 PAPS patients (31 naïve) and 132 CG (108 naïve) with comparable age (p=0.982) and sex (p>0.999). At D69, both groups had high and comparable SC (83.9% vs. 93.5%, p=0.092), as well as NAb positivity (77.4% vs. 78.7%, p=0.440), and NAb-activity (64.3% vs. 60.9%, p=0.689). Thrombotic events up to 6 months or other moderate/severe side effects were not observed. PAPS patients remained with stable aPL levels throughout the study at D0 vs. D28 vs. D69: anticardiolipin (aCL) IgG (p=0.058) and IgM (p=0.091); anti-beta-2 glycoprotein I (aβ2GPI) IgG (p=0.513) and IgM (p=0.468).We provided novel evidence that Sinovac-CoronaVac has high immunogenicity and safety profile in PAPS. Furthermore, Sinovac-CoronaVac did not trigger thrombosis nor induced changes in aPL production.

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