NK cell frequencies, function and correlates to vaccine outcome in BNT162b2 mRNA anti-SARS-CoV-2 vaccinated healthy and immunocompromised individuals
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Published:2022-02-08
Issue:1
Volume:28
Page:
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ISSN:1076-1551
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Container-title:Molecular Medicine
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language:en
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Short-container-title:Mol Med
Author:
Cuapio Angelica, Boulouis Caroline, Filipovic Iva, Wullimann David, Kammann Tobias, Parrot Tiphaine, Chen Puran, Akber Mira, Gao Yu, Hammer Quirin, Strunz Benedikt, Pérez Potti André, Rivera Ballesteros Olga, Lange Joshua, Muvva Jagadeeswara Rao, Bergman Peter, Blennow Ola, Hansson Lotta, Mielke Stephan, Nowak Piotr, Söderdahl Gunnar, Österborg Anders, Smith C. I. Edvard, Bogdanovic Gordana, Muschiol Sandra, Hellgren Fredrika, Loré Karin, Sobkowiak Michal J., Gabarrini Giorgio, Healy Katie, Sällberg Chen Margaret, Alici Evren, Björkström Niklas K., Buggert Marcus, Ljungman Per, Sandberg Johan K., Aleman Soo, Ljunggren Hans-GustafORCID
Abstract
AbstractAdaptive immune responses have been studied extensively in the course of mRNA vaccination against COVID-19. Considerably fewer studies have assessed the effects on innate immune cells. Here, we characterized NK cells in healthy individuals and immunocompromised patients in the course of an anti-SARS-CoV-2 BNT162b2 mRNA prospective, open-label clinical vaccine trial. See trial registration description in notes. Results revealed preserved NK cell numbers, frequencies, subsets, phenotypes, and function as assessed through consecutive peripheral blood samplings at 0, 10, 21, and 35 days following vaccination. A positive correlation was observed between the frequency of NKG2C+ NK cells at baseline (Day 0) and anti-SARS-CoV-2 Ab titers following BNT162b2 mRNA vaccination at Day 35. The present results provide basic insights in regards to NK cells in the context of mRNA vaccination, and have relevance for future mRNA-based vaccinations against COVID-19, other viral infections, and cancer.Trial registration: The current study is based on clinical material from the COVAXID open-label, non-randomized prospective clinical trial registered at EudraCT and clinicaltrials.gov (no. 2021–000175-37). Description: https://clinicaltrials.gov/ct2/show/NCT04780659?term=2021-000175-37&draw=2&rank=1.
Funder
Knut och Alice Wallenbergs Stiftelse Nordstjernan AB Region Stockholm Swedish Research Council Karolinska Institutet Karolinska Institute
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine
Reference32 articles.
1. Arunachalam PS, Scott MKD, Hagan T, Li C, Feng Y, Wimmers F, et al. Systems vaccinology of the BNT162b2 mRNA vaccine in humans. Nature. 2021;596(7872):410–6. 2. Baden LR, El Sahly HM, Essink B, Kotloff K, Frey S, Novak R, et al. Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine. N Engl J Med. 2021;384(5):403–16. 3. Bergman P, Blennow O, Hansson L, Mielke S, Nowak P, Chen P, et al. Safety and efficacy of the mRNA BNT162b2 vaccine against SARS-CoV-2 in five groups of immunocompromised patients and healthy controls in a prospective open-label clinical trial. EBioMedicine. 2021;74:103705. 4. Bjorkstrom NK, Lindgren T, Stoltz M, Fauriat C, Braun M, Evander M, et al. Rapid expansion and long-term persistence of elevated NK cell numbers in humans infected with hantavirus. J Exp Med. 2011;208(1):13–21. 5. Bjorkstrom NK, Strunz B, Ljunggren HG. Natural killer cells in antiviral immunity. Nat Rev Immunol. 2021;22:112–123. https://doi.org/10.1038/s41577-021-00558-3.
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