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mRNA 疫苗接种诱导针对 SARS-CoV-2 的多功能肺驻留记忆 T 细胞的能力有限,与感染相比。

Limited induction of polyfunctional lung-resident memory T cells against SARS-CoV-2 by mRNA vaccination compared to infection.

机构信息

Infectious Diseases Department, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.

Thoracic Surgery and Lung Transplantation Department, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.

出版信息

Nat Commun. 2023 Apr 5;14(1):1887. doi: 10.1038/s41467-023-37559-w.

DOI:10.1038/s41467-023-37559-w
PMID:37019909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10074357/
Abstract

Resident memory T cells (T) present at the respiratory tract may be essential to enhance early SARS-CoV-2 viral clearance, thus limiting viral infection and disease. While long-term antigen-specific T are detectable beyond 11 months in the lung of convalescent COVID-19 patients, it is unknown if mRNA vaccination encoding for the SARS-CoV-2 S-protein can induce this frontline protection. Here we show that the frequency of CD4 T cells secreting IFNγ in response to S-peptides is variable but overall similar in the lung of mRNA-vaccinated patients compared to convalescent-infected patients. However, in vaccinated patients, lung responses present less frequently a T phenotype compared to convalescent infected individuals and polyfunctional CD107a IFNγ T are virtually absent in vaccinated patients. These data indicate that mRNA vaccination induces specific T cell responses to SARS-CoV-2 in the lung parenchyma, although to a limited extend. It remains to be determined whether these vaccine-induced responses contribute to overall COVID-19 control.

摘要

呼吸道内存在的驻留记忆 T 细胞(T 细胞)可能对于增强早期 SARS-CoV-2 病毒清除至关重要,从而限制病毒感染和疾病。虽然在 COVID-19 恢复期患者的肺部中可检测到超过 11 个月的长期抗原特异性 T 细胞,但尚不清楚编码 SARS-CoV-2 S 蛋白的 mRNA 疫苗是否可以诱导这种一线保护。在这里,我们表明,与恢复期感染患者相比,mRNA 疫苗接种患者肺部中针对 S 肽产生 IFNγ 的 CD4 T 细胞的频率存在差异,但总体上相似。然而,与恢复期感染个体相比,在接种疫苗的患者中,肺部反应中 T 细胞表型出现的频率较低,并且在接种疫苗的患者中几乎不存在多功能 CD107a IFNγ T 细胞。这些数据表明,mRNA 疫苗可在肺实质中诱导针对 SARS-CoV-2 的特异性 T 细胞反应,但程度有限。尚需确定这些疫苗诱导的反应是否有助于整体 COVID-19 控制。

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