
Vaccines, Год журнала: 2025, Номер 13(4), С. 396 - 396
Опубликована: Апрель 9, 2025
Background: In response to the SARS-CoV-2 pandemic, a massive vaccination campaign was launched. Nonetheless, concerns arose regarding some peculiar groups of patients, including those affected by Systemic Lupus Erythematosus (SLE), because immune-suppressive drugs routinely administered patients and risk possible disease flares. Since effects third booster in SLE have been poorly assessed, this study aims evaluate immunogenicity safety BNT162b2 vaccine dose, together with immunosuppressive drugs. Methods: A monocentric cohort age- sex-matched healthy controls (HCs) (all vaccinated three homologous doses) were consecutively enrolled 6 months (T1) after their shot. Vaccine evaluated analyzing humoral cellular immune responses at T1 12 (T2). assessing adverse events related (T0) comparing activity among T0, T1, T2. Effects assessed stratifying according therapy vaccination: (1) receiving (IS) or (2) not (Non-IS). Results: At comparable between HC subjects, while significantly higher (p = 0.01). No differences found T2 cohorts. Similarly, both T2, IS Non-IS comparable. Moreover, lupus flares limited mostly mild, no life-threatening reported. Conclusions: The is safe induces an response, which persistent ongoing
Язык: Английский