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Longitudinal Comparison of Three T-Cell Assays and Three Antibody Assays Against SARS-CoV-2 Following Homologous mRNA-1273/mRNA-1273/mRNA-1273 and Heterologous ChAdOx1/ChAdOx1/BNT162b2 Vaccination: A Prospective Cohort in Naïve Healthcare Workers.

作者信息

Lee Hyeyoung, Ko Geon Young, Lee Jihyun, Bae Hyunjoo, Ryu Ji Hyeong, Jung Jin, Kang Hyunhye, Lee Raeseok, Lee Dong-Gun, Oh Eun-Jee

机构信息

Department of Laboratory Medicine, International St. Mary's Hospital, College of Medicine, Catholic Kwandong University, Incheon 22711, Republic of Korea.

Department of Medical Sciences, Graduate School of The Catholic University of Korea, Seoul 06591, Republic of Korea.

出版信息

Vaccines (Basel). 2024 Nov 29;12(12):1350. doi: 10.3390/vaccines12121350.


DOI:10.3390/vaccines12121350
PMID:39772013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11679843/
Abstract

: Cellular and humoral immunity are key to the immune response against SARS-CoV-2, but the comparability and correlation across different assays remain underexplored. This study compares three T-cell and three antibody assays in two vaccine groups. : This prospective longitudinal cohort study involved 46 naïve healthcare workers: a total of 11 in the homologous mRNA-1273 group (three doses) and 35 in the heterologous ChAd group (two ChAd doses followed by a BNT booster). Blood samples were collected at five time points. Cellular immunity was assessed using ELISPOT and two commercial interferon-gamma release assays: (IGRA)-QuantiFERON SARS-CoV-2 (QF) and Covi-FERON ELISA (CoVF). Humoral immunity was evaluated using total and IgG antibody assays and a surrogate virus neutralization test. : The mRNA-1273 group exhibited stronger and more consistent responses than the ChAd group. The correlations between ELISPOT and IGRA varied from weak to moderate (ρ = 0.300-0.410), while QF-IGRA and CoVF-IGRA showed stronger correlations (ρ = 0.700-0.737). The ELISPOT assay showed substantial agreement with QF [Ag2]-IGRA (k = 0.697-0.774) and CoVF [O-sp]-IGRA (k = 0.641-0.718), and an 80.4% agreement rate (k = 0.608) was found between the QF [Ag2]- and CoVF [O-sp]-IGRA tests. Three antibody assays demonstrated very strong correlations with each other and substantial to near-perfect agreement with ELISPOT (k = 0.866-0.949), QF [Ag2]-IGRA (k = 0.807-0.831), and CoVF [O-sp]-IGRA (k = 0.753-0.777). : SARS-CoV-2-specific cellular and antibody responses vary by platform and vaccine type, highlighting the importance of measuring both T-cell and B-cell responses using multiple assays to comprehensively assess immune status.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/65bb6275e4be/vaccines-12-01350-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/34721681bdf8/vaccines-12-01350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/926a5bdf0b82/vaccines-12-01350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/5c4fcf51efa2/vaccines-12-01350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/398fc6ae8a24/vaccines-12-01350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/dc0fd6ce0f60/vaccines-12-01350-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/3852f462e563/vaccines-12-01350-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/65bb6275e4be/vaccines-12-01350-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/34721681bdf8/vaccines-12-01350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/926a5bdf0b82/vaccines-12-01350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/5c4fcf51efa2/vaccines-12-01350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/398fc6ae8a24/vaccines-12-01350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/dc0fd6ce0f60/vaccines-12-01350-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/3852f462e563/vaccines-12-01350-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee41/11679843/65bb6275e4be/vaccines-12-01350-g007.jpg

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Longitudinal Comparison of Three T-Cell Assays and Three Antibody Assays Against SARS-CoV-2 Following Homologous mRNA-1273/mRNA-1273/mRNA-1273 and Heterologous ChAdOx1/ChAdOx1/BNT162b2 Vaccination: A Prospective Cohort in Naïve Healthcare Workers.

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本文引用的文献

[1]
Vaccine-induced humoral response of BNT162b2 and mRNA-1273 against BA.1, BA.5, and XBB.1.5. (sub)variants 6 months after a homologous booster: is immunogenicity equivalent?

Heliyon. 2024-8-10

[2]
Application of Interferon-γ Release Assay in the Assessment of T-Cell Immunity to SARS-CoV-2 Antigens in the Cohort of Pediatric Patients with Juvenile Idiopathic Arthritis.

Children (Basel). 2024-6-16

[3]
SARS-CoV-2-specific T cell responses: a comparative analysis between QuantiFERON SARS-CoV-2, T-SPOT.COVID, and an in-house Omicron ELISpot.

J Virol Methods. 2024-6

[4]
Evaluation of Long-Term Adaptive Immune Responses Specific to SARS-CoV-2: Effect of Various Vaccination and Omicron Exposure.

Vaccines (Basel). 2024-3-13

[5]
Prolonged SARS-CoV-2 T Cell Responses in a Vaccinated COVID-19-Naive Population.

Vaccines (Basel). 2024-3-4

[6]
A quest for universal anti-SARS-CoV-2 T cell assay: systematic review, meta-analysis, and experimental validation.

NPJ Vaccines. 2024-1-2

[7]
Longitudinal Analysis of SARS-CoV-2-Specific Cellular and Humoral Immune Responses and Breakthrough Infection following BNT162b2/BNT162b2/BNT162b2 and ChAdOx1/ChAdOx1/BNT162b2 Vaccination: A Prospective Cohort in Naive Healthcare Workers.

Vaccines (Basel). 2023-10-19

[8]
Comparison of Four T-cell Assays and Two Binding Antibody Assays in SARS-CoV-2 Vaccinees With or Without Omicron Breakthrough Infection.

Ann Lab Med. 2023-11-1

[9]
Waning cellular immune responses and predictive factors in maintaining cellular immunity against SARS-CoV-2 six months after BNT162b2 mRNA vaccination.

Sci Rep. 2023-6-13

[10]
Improved Performance of the QuantiFERON-SARS-CoV-2 Assay with the Extended Set.

Viruses. 2023-5-17

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