AUTHOR=Graydon Elizabeth K. , Conner Tonia L. , Dunham Kim , Olsen Cara , Goguet Emilie , Coggins Si’Ana A. , Rekedal Marana , Samuels Emily , Jackson-Thompson Belinda , Moser Matthew , Lindrose Alyssa , Hollis-Perry Monique , Wang Gregory , Maiolatesi Santina , Alcorta Yolanda , Reyes Anatalio , Wong Mimi , Ramsey Kathy , Davies Julian , Parmelee Edward , Ortega Orlando , Sanchez Mimi , Moller Sydney , Inglefield Jon , Tribble David , Burgess Timothy , O’Connell Robert , Malloy Allison M. W. , Pollett Simon , Broder Christopher C. , Laing Eric D. , Anderson Stephen K. , Mitre Edward TITLE=Natural killer cells and BNT162b2 mRNA vaccine reactogenicity and durability JOURNAL=Frontiers in Immunology VOLUME=14 YEAR=2023 URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2023.1225025 DOI=10.3389/fimmu.2023.1225025 ISSN=1664-3224 ABSTRACT=Introduction

Natural killer (NK) cells can both amplify and regulate immune responses to vaccination. Studies in humans and animals have observed NK cell activation within days after mRNA vaccination. In this study, we sought to determine if baseline NK cell frequencies, phenotype, or function correlate with antibody responses or inflammatory side effects induced by the Pfizer-BioNTech COVID-19 vaccine (BNT162b2).

Methods

We analyzed serum and peripheral blood mononuclear cells (PBMCs) from 188 participants in the Prospective Assessment of SARS-CoV-2 Seroconversion study, an observational study evaluating immune responses in healthcare workers. Baseline serum samples and PBMCs were collected from all participants prior to any SARS-CoV-2 infection or vaccination. Spike-specific IgG antibodies were quantified at one and six months post-vaccination by microsphere-based multiplex immunoassay. NK cell frequencies and phenotypes were assessed on pre-vaccination PBMCs from all participants by multi-color flow cytometry, and on a subset of participants at time points after the 1st and 2nd doses of BNT162b2. Inflammatory side effects were assessed by structured symptom questionnaires, and baseline NK cell functionality was quantified by an in vitro killing assay on participants that reported high or low post-vaccination symptom scores.

Results

Key observations include: 1) circulating NK cells exhibit evidence of activation in the week following vaccination, 2) individuals with high symptom scores after 1st vaccination had higher pre-vaccination NK cytotoxicity indices, 3) high pre-vaccination NK cell numbers were associated with lower spike-specific IgG levels six months after two BNT162b2 doses, and 4) expression of the inhibitory marker NKG2A on immature NK cells was associated with higher antibody responses 1 and 6 months post-vaccination.

Discussion

These results suggest that NK cell activation by BNT162b2 vaccination may contribute to vaccine-induced inflammatory symptoms and reduce durability of vaccine-induced antibody responses.