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亚洲脸红基因变体增强新冠疫苗的细胞免疫原性:日本普通人群的前瞻性观察

Asian Flush Gene Variant Enhances Cellular Immunogenicity of COVID-19 Vaccine: Prospective Observation in the Japanese General Population.

作者信息

Bogahawaththa Sudarma, Hara Megumi, Furukawa Takuma, Iwasaka Chiharu, Sawada Takeshi, Yamada Goki, Tokiya Mikiko, Kitagawa Kyoko, Miyake Yasunobu, Kido Mizuho Aoki, Hirota Yoshio, Matsumoto Akiko

机构信息

Laboratory of Biochemistry, Department of Applied Biochemistry and Food Science, Faculty of Agriculture, Saga University, Honjo, Saga 840-8502, Japan.

Department of Social and Environmental Medicine, Saga University, Nabeshima, Saga 840-8501, Japan.

出版信息

Vaccines (Basel). 2024 Sep 5;12(9):1015. doi: 10.3390/vaccines12091015.

DOI:10.3390/vaccines12091015
PMID:39340045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11435883/
Abstract

We previously reported a reduced humoral immune response to the COVID-19 vaccines. Subsequently, we observed a lower susceptibility to COVID-19 in individuals carrying the rs671 variant through a web-based retrospective survey. Based on these findings, we hypothesized that rs671 variant was beneficial for cellular immunity against COVID-19. Using the IFN-γ enzyme-linked immunospot (ELISPOT) assay, we assessed cellular immunity before and after COVID-19 vaccination in two subcohorts of a previously reported cohort. Subcohort 1 (26 participants) had six repeated observations at baseline after one to three doses, whereas subcohort 2 (19 participants) had two observations before and after the third dose. ELISPOT counts at six months after the second dose increased from baseline in carriers of the rs671 variant but not in non-carriers. A positive effect of rs671 on ELISPOT counts was estimated using a mixed model (183 observations from 45 participants), including the random effect of subcohort, repeated measures, and fixed effects of vaccine type, age, sex, height, lifestyle, steroid use, and allergic disease. There was no association between ELISPOT counts and specific IgG levels, suggesting a limitation in estimating protective potential by humoral response. Our sequential observational studies suggest a beneficial effect of the rs671 variant in SARS-CoV-2 infection via enhanced cellular immune response, providing a potential basis for optimizing preventive measures and drug development.

摘要

我们之前报道过对新冠疫苗的体液免疫反应降低。随后,我们通过一项基于网络的回顾性调查观察到,携带rs671变体的个体对新冠病毒的易感性较低。基于这些发现,我们推测rs671变体对针对新冠病毒的细胞免疫有益。我们使用干扰素-γ酶联免疫斑点(ELISPOT)试验,在先前报道队列的两个亚组中评估了新冠疫苗接种前后的细胞免疫。亚组1(26名参与者)在接种一至三剂疫苗后的基线时有6次重复观察,而亚组2(19名参与者)在第三剂疫苗接种前后各有2次观察。rs671变体携带者在第二剂疫苗接种后六个月的ELISPOT计数较基线有所增加,而非携带者则没有。使用混合模型(来自45名参与者的183次观察)估计了rs671对ELISPOT计数的积极影响,该模型包括亚组的随机效应、重复测量,以及疫苗类型、年龄、性别、身高、生活方式、类固醇使用和过敏性疾病的固定效应。ELISPOT计数与特异性IgG水平之间没有关联,这表明通过体液反应估计保护潜力存在局限性。我们的系列观察性研究表明,rs671变体通过增强细胞免疫反应对新冠病毒感染具有有益作用,为优化预防措施和药物开发提供了潜在依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659d/11435883/90e1bca10347/vaccines-12-01015-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659d/11435883/86682aaafb68/vaccines-12-01015-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659d/11435883/650885a5184e/vaccines-12-01015-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659d/11435883/90e1bca10347/vaccines-12-01015-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659d/11435883/86682aaafb68/vaccines-12-01015-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659d/11435883/650885a5184e/vaccines-12-01015-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659d/11435883/90e1bca10347/vaccines-12-01015-g003.jpg

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Infection burden and ALDH2 rs671, East Asian genetic diversity: A reply.感染负担与乙醛脱氢酶2基因rs671、东亚遗传多样性:一则回应
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