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在朱拉隆功医院评估 ChAdox1 nCov-19(AZD1222)疫苗在实体瘤癌症患者中的免疫原性。

Immunogenicity evaluation of ChAdox1 nCov-19 (AZD1222) vaccine in solid cancer patients in Chulabhorn Hospital.

机构信息

Division of Medical Oncology, Chulabhorn Hospital, Chulabhorn Royal Academy, Bangkok, Thailand.

Princess Srisavangavadhana College of Medicine, Chulabhorn Royal Academy, Bangkok, Thailand.

出版信息

Hum Vaccin Immunother. 2022 Nov 30;18(6):2104058. doi: 10.1080/21645515.2022.2104058. Epub 2022 Aug 17.

DOI:10.1080/21645515.2022.2104058
PMID:35976687
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9746434/
Abstract

INTRODUCTION

Cancer patients are more vulnerable to coronavirus disease 2019 (COVID-19) owing to their compromised immune status. However, data regarding COVID-19 vaccine safety and immune response in cancer patients are scarce.

METHOD

This prospective, age- and sex-matched, single-center cohort study included 61 cancer patients and 122 healthy control participants. Seropositivity was defined as anti-S IgG titer >0.8 units/ml. Primary end point was seroconversion rate of immunoglobulin (Ig)G antibodies against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S) protein (anti-S IgG) in cancer patients vs. healthy control participants following the second dose of COVID-19 vaccine ChAdOx1 nCoV-19 (AZD1222).

RESULTS

After the second-dose vaccination, there was no difference in seropositivity rate between groups (57 [93.44%] patients with cancer vs. 121 [99.18%] control participants; geometric mean ratio [GMR]: 0.39; 95%CI: 0.01-10.46; -value = 0.571). In contrast, after the first-dose vaccination, the seropositivity rate was significantly lower in the cancer patients than in the control participants (50/61 [81.97%] vs. 121/122 [99.18%]; GMR: 0.07; 95%CI: 0.01-0.71; p = 0.025). The median anti-S IgG titer after the first-and second dose vaccination were not significantly different between groups. Female sex was significantly associated with a higher anti-S IgG titer. 5FU- and taxane-based chemotherapy regimens were associated with a lower IgG titer. Side effects of vaccination were tolerable.

CONCLUSIONS

The anti-S IgG seropositivity rate after completing the second vaccine dose did not differ between the cancer patients and control participants. However, the anti-S IgG seropositivity rate after the first-dose vaccination was lower in cancer patients.

摘要

简介

由于免疫功能受损,癌症患者更容易感染 2019 年冠状病毒病(COVID-19)。然而,关于癌症患者 COVID-19 疫苗安全性和免疫反应的数据仍然有限。

方法

本前瞻性、年龄和性别匹配的单中心队列研究纳入了 61 例癌症患者和 122 例健康对照者。血清阳性定义为抗-S IgG 滴度>0.8 单位/ml。主要终点是癌症患者和健康对照者在接种第二剂 COVID-19 疫苗 ChAdOx1 nCoV-19(AZD1222)后针对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突(S)蛋白的免疫球蛋白(IgG)抗体的血清转化率(抗-S IgG)。

结果

在第二剂疫苗接种后,两组的血清阳性率没有差异(57 [93.44%] 例癌症患者与 121 [99.18%] 例对照参与者;几何均数比[GMR]:0.39;95%CI:0.01-10.46;p 值=0.571)。相反,在第一剂疫苗接种后,癌症患者的血清阳性率明显低于对照组(50/61 [81.97%] 与 121/122 [99.18%];GMR:0.07;95%CI:0.01-0.71;p=0.025)。两组之间第一剂和第二剂疫苗接种后的抗-S IgG 滴度中位数没有显著差异。女性性别与更高的抗-S IgG 滴度显著相关。5FU 和紫杉烷类化疗方案与较低的 IgG 滴度相关。疫苗接种的副作用可耐受。

结论

完成第二剂疫苗接种后,癌症患者和对照组的抗-S IgG 血清阳性率没有差异。然而,癌症患者在接种第一剂疫苗后,抗-S IgG 血清阳性率较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a4/9746434/baaebd6002e5/KHVI_A_2104058_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a4/9746434/baaebd6002e5/KHVI_A_2104058_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a4/9746434/baaebd6002e5/KHVI_A_2104058_F0001_OC.jpg

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