Department of Medicine, Queen Mary Hospital, School of Clinical Medicine, The University of Hong Kong, Hong Kong.
Department of Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Clin Mol Hepatol. 2022 Jul;28(3):553-564. doi: 10.3350/cmh.2022.0082. Epub 2022 May 11.
BACKGROUND/AIMS: Studies of hepatic steatosis (HS) effect on COVID-19 vaccine immunogenicity are lacking. We aimed to compare immunogenicity of BNT162b2 and CoronaVac among moderate/severe HS and control subjects.
Two hundred ninety-five subjects who received BNT162b2 or CoronaVac vaccines from five vaccination centers were categorized into moderate/severe HS (controlled attenuation parameter ≥268 dB/m on transient elastography) (n=74) or control (n=221) groups. Primary outcomes were seroconversion rates of neutralising antibody by live virus Microneutralization (vMN) assay (titer ≥10) at day21 (BNT162b2) or day28 (CoronaVac) and day56 (both). Secondary outcome was highest-tier titer response (top 25% of vMN titer; cutoff: 160 [BNT162b2] and 20 [CoronaVac]) at day 56.
For BNT162b2 (n=228, 77.3%), there was no statistical differences in seroconversion rates (day21: 71.7% vs. 76.6%; day56: 100% vs. 100%) or vMN geometric mean titer (GMT) (day21: 13.2 vs. 13.3; day56: 91.9 vs. 101.4) among moderate/severe HS and control groups respectively. However, lower proportion of moderate/severe HS patients had highest-tier response (day56: 5.0% vs. 15.5%; P=0.037). For CoronaVac (n=67, 22.7%), there was no statistical differences in seroconversion rates (day21: 7.1% vs. 15.1%; day56: 64.3% vs. 83.0%) or vMN GMT (5.3 vs. 5.8,) at day28. However, moderate/severe HS patients had lower vMN GMT (9.1 vs. 14.8, P=0.021) at day 56 with lower proportion having highest-tier response (21.4% vs. 52.8%, P=0.036).
While there was no difference in seroconversion rate between moderate/severe HS and control groups after two doses of vaccine, a lower proportion of moderate/severe HS patients achieved highest-tier response for either BNT162b2 or CoronaVac.
背景/目的:目前缺乏关于肝脂肪变性(HS)对 COVID-19 疫苗免疫原性影响的研究。我们旨在比较中重度 HS 患者和对照组接受 BNT162b2 和 CoronaVac 疫苗的免疫原性。
295 名在五家接种中心接受 BNT162b2 或 CoronaVac 疫苗的受试者被分为中重度 HS 组(瞬时弹性成像受控衰减参数≥268 dB/m)(n=74)或对照组(n=221)。主要结局为在第 21 天(BNT162b2)或第 28 天(CoronaVac)和第 56 天(两者)的活病毒微量中和(vMN)检测(滴度≥10)的中和抗体血清转化率。次要结局为第 56 天的最高滴度反应(最高 25%的 vMN 滴度;截止值:160[BNT162b2]和 20[CoronaVac])。
对于 BNT162b2(n=228,77.3%),在血清转化率(第 21 天:71.7% vs. 76.6%;第 56 天:100% vs. 100%)或 vMN 几何平均滴度(GMT)(第 21 天:13.2 vs. 13.3;第 56 天:91.9 vs. 101.4)方面,中重度 HS 组和对照组之间均无统计学差异。然而,中重度 HS 患者中具有最高滴度反应的比例较低(第 56 天:5.0% vs. 15.5%;P=0.037)。对于 CoronaVac(n=67,22.7%),在血清转化率(第 21 天:7.1% vs. 15.1%;第 56 天:64.3% vs. 83.0%)或 vMN GMT(5.3 vs. 5.8)方面,第 28 天均无统计学差异。然而,中重度 HS 患者在第 56 天的 vMN GMT 较低(9.1 vs. 14.8,P=0.021),且具有最高滴度反应的比例较低(21.4% vs. 52.8%,P=0.036)。
尽管在接种两剂疫苗后,中重度 HS 组和对照组的血清转化率无差异,但对于 BNT162b2 或 CoronaVac,中重度 HS 患者中具有最高滴度反应的比例较低。