第三剂BNT162b2疫苗在肝脏移植和健康青少年中的安全性和有效性

Palittiya Sintusek, Supranee Buranapraditkun, Siriporn Khunsri, Thanunrat Thongmee, Preeyaporn Vichaiwattana, Warunee Polsawat, Yong Poovorawan
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摘要

目的:根据我们之前的研究,2剂量的bnt162b2疫苗对Omicron变体的效果较差。本研究旨在评估3剂量bnt162b2疫苗在肝移植(LT)和健康青少年中的安全性和有效性。方法:LT和符合纳入标准的健康青少年接受第三剂BNT162b2疫苗(30µg)。评估抗受体结合域免疫球蛋白和t细胞对严重急性呼吸综合征冠状病毒2尖峰肽的特异性反应,在第三次给药前3个月(访- 1),第三次给药后0(访0),1(访1)和2个月(访2)。抗核衣壳免疫球蛋白和中和抗体在第0次和第1次就诊时进行评估。监测不良事件(ae)。结果:11名LT和14名健康青少年(14.64(13.2,15.7)岁,其中男性占44.2%)在访诊时抗受体结合域免疫球蛋白几何平均滴度分别为1412.47(95%可信区间[CI], 948.18-2041.11)和1235.79 (95% CI, 901.07-1705.73) U/mL,但分别上升至38 587.76 (95% CI, 24 628.03-60 460.18)和29 222.38 (95% CI, 16 291.72-52 401.03) U/mL (P <0.05)。这与中和抗体(42.29%和95.37% vs 44.65%和91.68%)一致,P <0.001),以及随访0和随访1时LT和健康青少年的干扰素γ分泌细胞。对于严重的ae,一名患有自身免疫重叠综合征的LT女孩在接种疫苗后5个月死于急性肝衰竭。结论:在LT和健康青少年中,接种3剂量bnt162b2疫苗后,体液和细胞免疫反应都很高。然而,在患有自身免疫性疾病的LT青少年中,怀疑存在严重的ae。
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Safety and Efficacy of a Third Dose of the BNT162b2 Vaccine in Liver-Transplanted and Healthy Adolescents
Objectives: According to our previous study, the 2-dose-BNT162b2 vaccination is less effective against the Omicron variant. This study aimed to assess the safety and efficacy of a 3-dose-BNT162b2 vaccination in liver-transplanted (LT) and healthy adolescents. Methods: LT and healthy adolescents who met the inclusion criteria received a third dose of the BNT162b2 vaccine (30 µg). Antireceptor-binding domain immunoglobulin and T-cell-specific responses to severe acute respiratory syndrome coronavirus 2 spike peptides were assessed 3 months before the third dose (Visit −1) and 0 (Visit 0), 1 (Visit 1), and 2 months (Visit 2) after the third dose. Antinucleocapsid immunoglobulin and neutralizing antibodies were assessed at Visits 0 and 1. Adverse events (AEs) were monitored. Results: Eleven LT and 14 healthy adolescents aged 14.64 (13.2, 15.7) years (44.2% male) had antireceptor-binding domain immunoglobulin geometric mean titers of 1412.47 (95% confidence interval [CI], 948.18–2041.11) and 1235.79 (95% CI, 901.07–1705.73) U/mL at Visit −1 but increased to 38 587.76 (95% CI, 24 628.03–60 460.18) and 29 222.38 (95% CI, 16 291.72–52 401.03) U/mL ( P < 0.05) at Visit 1, respectively. This was consistent with neutralizing antibodies (42.29% and 95.37% vs 44.65% and 91.68%, P < 0.001) and interferon-γ-secreting cells in LT and healthy adolescents at Visit 0 versus Visit 1, respectively. For serious AEs, an LT girl with autoimmune overlap syndrome died 5 months postvaccination from acute liver failure. Conclusions: In both LT and healthy adolescents, humoral and cellular immune responses were high after the 3-dose-BNT162b2 vaccination. However, serious AEs were suspected in LT adolescents with autoimmune diseases.
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