Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/48669
Title: Increment of immunogenicity after third dose of a homologous inactivated SARS-CoV-2 vaccine in a large population of patients with autoimmune rheumatic diseases
Authors: AIKAWA, Nadia EmiKUPA, Leonard de Vinci KandaMEDEIROS-RIBEIRO, Ana CristinaSAAD, Carla Goncalves SchahinYUKI, Emily Figueiredo NevesPASOTO, Sandra GofinetROJO, Priscila TagliaferroPEREIRA, Rosa Maria RodriguesSHINJO, Samuel KatsuyukiSAMPAIO-BARROS, Percival DegravaANDRADE, Danieli Castro OliveiraHALPERN, Ari Stiel RaduFULLER, RicardoSOUZA, Fernando Henrique CarlosGUEDES, Lissiane Karine NoronhaASSAD, Ana Paula LuppinoMORAES, Julio Cesar Bertacini deLOPES, Michelle Remiao UgoliniMARTINS, Victor Adriano de OliveiraBETANCOURT, LorenaRIBEIRO, Carolina TorresSALES, Lucas PeixotoBERTOGLIO, Isabela MariaBONOLDI, Virginia Lucia NazarioMELLO, Renata Lys PinheiroBALBI, Gustavo Guimaraes MoreiraSARTORI, Ana Marli ChristovamANTONANGELO, LeilaSILVA, Clovis ArturBONFA, Eloisa
Citation: ANNALS OF THE RHEUMATIC DISEASES, v.81, n.7, p.1036-1043, 2022
Abstract: Objective To determine the immunogenicity of the third dose of CoronaVac vaccine in a large population of patients with autoimmune rheumatic diseases (ARD) and the factors associated with impaired response. Methods Adult patients with ARD and age-balanced/sex-balanced controls (control group, CG) previously vaccinated with two doses of CoronaVac received the third dose at D210 (6 months after the second dose). The presence of anti-SARS-CoV-2 S1/S2 IgG and neutralising antibodies (NAb) was evaluated previously to vaccination (D210) and 30 days later (D240). Patients with controlled disease suspended mycophenolate mofetil (MMF) for 7 days or methotrexate (MTX) for 2 weekly doses after vaccination. Results ARD (n=597) and CG (n=199) had comparable age (p=0.943). Anti-S1/S2 IgG seropositivity rates significantly increased from D210 (60%) to D240 (93%) (p<0.0001) in patients with ARD. NAb positivity also increased: 38% (D210) vs 81.4% (D240) (p<0.0001). The same pattern was observed for CG, with significantly higher frequencies for both parameters at D240 (p<0.05). Multivariate logistic regression analyses in the ARD group revealed that older age (OR=0.98, 95% CI 0.96 to 1.0, p=0.024), vasculitis diagnosis (OR=0.24, 95% CI 0.11 to 0.53, p<0.001), prednisone >= 5 mg/day (OR=0.46, 95% CI 0.27 to 0.77, p=0.003), MMF (OR=0.30, 95% CI 0.15 to 0.61, p<0.001) and biologics (OR=0.27, 95% CI 0.16 to 0.46, p<0.001) were associated with reduced anti-S1/S2 IgG positivity. Similar analyses demonstrated that prednisone >= 5 mg/day (OR=0.63, 95% CI 0.44 to 0.90, p=0.011), abatacept (OR=0.39, 95% CI 0.20 to 0.74, p=0.004), belimumab (OR=0.29, 95% CI 0.13 to 0.67, p=0.004) and rituximab (OR=0.11, 95% CI 0.04 to 0.30, p<0.001) were negatively associated with NAb positivity. Further evaluation of COVID-19 seronegative ARD at D210 demonstrated prominent increases in positivity rates at D240 for anti-S1/S2 IgG (80.5%) and NAb (59.1%) (p<0.0001). Conclusions We provide novel data on a robust response to the third dose of CoronaVac in patients with ARD, even in those with prevaccination COVID-19 seronegative status. Drugs implicated in reducing immunogenicity after the regular two-dose regimen were associated with non-responsiveness after the third dose, except for MTX.
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