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中重度肝脂肪变性对 BNT162b2 和科兴疫苗接种者中和抗体应答的影响。

Effect of moderate-to-severe hepatic steatosis on neutralising antibody response among BNT162b2 and CoronaVac recipients.

机构信息

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.

出版信息

Clin Mol Hepatol. 2022 Jul;28(3):553-564. doi: 10.3350/cmh.2022.0082. Epub 2022 May 11.

Abstract

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.

METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

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。

方法

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])。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f9/9293606/cfad64661430/cmh-2022-0082f1.jpg

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