Evaluation of the QuantiFERON SARS-CoV-2 interferon-ɣ release assay in mRNA-1273 vaccinated health care workers
•44 % of vaccinees had INF-ɣ levels above 015 IU/mL in response to stimulation.•100 % of vaccinees showed INF-ɣ levels above 0015 IU/mL in response to stimulation.•More studies are needed to set an appropriate cut-off for this convenient assay. Current studies focus on cellular and humoral immunity...
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| Vydané v: | Journal of virological methods Ročník 298; s. 114295 |
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| Jazyk: | English |
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Elsevier B.V
01.12.2021
Published by Elsevier B.V |
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| Abstract | •44 % of vaccinees had INF-ɣ levels above 015 IU/mL in response to stimulation.•100 % of vaccinees showed INF-ɣ levels above 0015 IU/mL in response to stimulation.•More studies are needed to set an appropriate cut-off for this convenient assay.
Current studies focus on cellular and humoral immunity induced by novel SARS-CoV-2 vaccines. Non-responders to vaccinations are not uncommonly encountered in clinical medicine (e.g. in the field of hepatitis B). Whereas vaccine-induced humoral immunity against SARS-CoV-2 is compromised by emerging Variants of Concern (VOCs), cellular immunity against SARS-CoV-2 is emerging as resilient against VOCs. Thus commercially available test kits for diagnostic laboratories designed to evaluate cellular immune responses to SARS-CoV-2 are urgently needed. Here we evaluated the novel QuantiFERON SARS-CoV-2 assay (Qiagen) measuring INF-ɣ release induced by two spike-derived peptide pools (Ag1 and Ag2) in a cohort of health care workers vaccinated with the mRNA-1273 vaccine and confirmed humoral response. Our study indicates the usefulness of this novel assay for routine laboratories to evaluate cellular immunity against SARS-CoV-2 in response to mRNA-1273 vaccination. |
|---|---|
| AbstractList | Current studies focus on cellular and humoral immunity induced by novel SARS-CoV-2 vaccines. Non-responders to vaccinations are not uncommonly encountered in clinical medicine (e.g. in the field of hepatitis B). Whereas vaccine-induced humoral immunity against SARS-CoV-2 is compromised by emerging Variants of Concern (VOCs), cellular immunity against SARS-CoV-2 is emerging as resilient against VOCs. Thus commercially available test kits for diagnostic laboratories designed to evaluate cellular immune responses to SARS-CoV-2 are urgently needed. Here we evaluated the novel QuantiFERON SARS-CoV-2 assay (Qiagen) measuring INF-ɣ release induced by two spike-derived peptide pools (Ag1 and Ag2) in a cohort of health care workers vaccinated with the mRNA-1273 vaccine and confirmed humoral response. Our study indicates the usefulness of this novel assay for routine laboratories to evaluate cellular immunity against SARS-CoV-2 in response to mRNA-1273 vaccination. Current studies focus on cellular and humoral immunity induced by novel SARS-CoV-2 vaccines. Non-responders to vaccinations are not uncommonly encountered in clinical medicine (e.g. in the field of hepatitis B). Whereas vaccine-induced humoral immunity against SARS-CoV-2 is compromised by emerging Variants of Concern (VOCs), cellular immunity against SARS-CoV-2 is emerging as resilient against VOCs. Thus commercially available test kits for diagnostic laboratories designed to evaluate cellular immune responses to SARS-CoV-2 are urgently needed. Here we evaluated the novel QuantiFERON SARS-CoV-2 assay (Qiagen) measuring INF-ɣ release induced by two spike-derived peptide pools (Ag1 and Ag2) in a cohort of health care workers vaccinated with the mRNA-1273 vaccine and confirmed humoral response. Our study indicates the usefulness of this novel assay for routine laboratories to evaluate cellular immunity against SARS-CoV-2 in response to mRNA-1273 vaccination.Current studies focus on cellular and humoral immunity induced by novel SARS-CoV-2 vaccines. Non-responders to vaccinations are not uncommonly encountered in clinical medicine (e.g. in the field of hepatitis B). Whereas vaccine-induced humoral immunity against SARS-CoV-2 is compromised by emerging Variants of Concern (VOCs), cellular immunity against SARS-CoV-2 is emerging as resilient against VOCs. Thus commercially available test kits for diagnostic laboratories designed to evaluate cellular immune responses to SARS-CoV-2 are urgently needed. Here we evaluated the novel QuantiFERON SARS-CoV-2 assay (Qiagen) measuring INF-ɣ release induced by two spike-derived peptide pools (Ag1 and Ag2) in a cohort of health care workers vaccinated with the mRNA-1273 vaccine and confirmed humoral response. Our study indicates the usefulness of this novel assay for routine laboratories to evaluate cellular immunity against SARS-CoV-2 in response to mRNA-1273 vaccination. •44 % of vaccinees had INF-ɣ levels above 015 IU/mL in response to stimulation.•100 % of vaccinees showed INF-ɣ levels above 0015 IU/mL in response to stimulation.•More studies are needed to set an appropriate cut-off for this convenient assay. Current studies focus on cellular and humoral immunity induced by novel SARS-CoV-2 vaccines. Non-responders to vaccinations are not uncommonly encountered in clinical medicine (e.g. in the field of hepatitis B). Whereas vaccine-induced humoral immunity against SARS-CoV-2 is compromised by emerging Variants of Concern (VOCs), cellular immunity against SARS-CoV-2 is emerging as resilient against VOCs. Thus commercially available test kits for diagnostic laboratories designed to evaluate cellular immune responses to SARS-CoV-2 are urgently needed. Here we evaluated the novel QuantiFERON SARS-CoV-2 assay (Qiagen) measuring INF-ɣ release induced by two spike-derived peptide pools (Ag1 and Ag2) in a cohort of health care workers vaccinated with the mRNA-1273 vaccine and confirmed humoral response. Our study indicates the usefulness of this novel assay for routine laboratories to evaluate cellular immunity against SARS-CoV-2 in response to mRNA-1273 vaccination. |
| ArticleNumber | 114295 |
| Author | Imöhl, Matthias Klingel, Hanna Kleines, Michael Haase, Gerhard Krüttgen, Alexander Haefner, Helga |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34555429$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.3201/eid2701.203611 10.1016/j.jinf.2021.03.010 10.1056/NEJMoa2001017 10.1016/j.jviromet.2020.113978 10.1016/j.jiac.2021.08.016 10.1038/s41586-020-2012-7 10.4161/hv.6.9.12420 10.1056/NEJMoa2028436 10.1172/JCI149335 10.1093/ndt/gfab064 10.1016/j.jviromet.2021.114122 10.1016/j.tube.2017.11.014 10.3389/fimmu.2021.676932 10.1038/s41586-021-03653-6 10.1016/j.humimm.2021.05.003 10.1097/MD.0000000000015228 |
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| SubjectTerms | 2019-nCoV Vaccine mRNA-1273 Antibodies, Viral cell-mediated immunity Cellular immunity COVID-19 COVID-19 Vaccines Health Personnel health services hepatitis B Humans humoral immunity Interferon-gamma Release Tests medicine peptides RNA, Messenger - genetics SARS-CoV-2 Serology Severe acute respiratory syndrome coronavirus 2 Vaccination vaccines |
| Title | Evaluation of the QuantiFERON SARS-CoV-2 interferon-ɣ release assay in mRNA-1273 vaccinated health care workers |
| URI | https://dx.doi.org/10.1016/j.jviromet.2021.114295 https://www.ncbi.nlm.nih.gov/pubmed/34555429 https://www.proquest.com/docview/2576649233 https://www.proquest.com/docview/2636622967 https://pubmed.ncbi.nlm.nih.gov/PMC8452154 |
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