TY - JOUR
T1 - Modulation of the Immune Response to Severe Acute Respiratory Syndrome Coronavirus 2 Vaccination by Nonsteroidal Anti-Inflammatory Drugs
AU - Skarke, Carsten
AU - Lordan, Ronan
AU - Barekat, Kayla
AU - Naik, Amruta
AU - Mathew, Divij
AU - Ohtani, Takuya
AU - Greenplate, Allison R.
AU - Grant, Gregory R.
AU - Lahens, Nicholas F.
AU - Gouma, Sigrid
AU - Troisi, Elizabeth
AU - Sengupta, Arjun
AU - Weljie, Aalim M.
AU - Meng, Wenzhao
AU - Luning Prak, Eline T.
AU - Lundgreen, Kendall
AU - Bates, Paul
AU - Meng, Hu
AU - FitzGerald, Garret A.
N1 - Publisher Copyright:
Copyright © 2023 by The Author(s).
PY - 2023/8/1
Y1 - 2023/8/1
N2 - Evidence is scarce to guide the use of nonsteroidal anti-inflammatory drugs (NSAIDs) to mitigate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine–related adverse effects, given the possibility of blunting the desired immune response. In this pilot study, we deeply phenotyped a small number of volunteers who did or did not take NSAIDs concomitant with SARS-CoV-2 immunizations to seek initial information on the immune response. A SARS-CoV-2 vaccine–specific receptor binding domain (RBD) IgG antibody response and efficacy in the evoked neutralization titers were evident irrespective of concomitant NSAID consumption. Given the sample size, only a large and consistent signal of immunomodulation would have been detectable, and this was not apparent. However, the information gathered may inform the design of a definitive clinical trial. Here we report a series of divergent omics signals that invites additional hypotheses testing.
AB - Evidence is scarce to guide the use of nonsteroidal anti-inflammatory drugs (NSAIDs) to mitigate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine–related adverse effects, given the possibility of blunting the desired immune response. In this pilot study, we deeply phenotyped a small number of volunteers who did or did not take NSAIDs concomitant with SARS-CoV-2 immunizations to seek initial information on the immune response. A SARS-CoV-2 vaccine–specific receptor binding domain (RBD) IgG antibody response and efficacy in the evoked neutralization titers were evident irrespective of concomitant NSAID consumption. Given the sample size, only a large and consistent signal of immunomodulation would have been detectable, and this was not apparent. However, the information gathered may inform the design of a definitive clinical trial. Here we report a series of divergent omics signals that invites additional hypotheses testing.
UR - https://www.scopus.com/pages/publications/85165222156
U2 - 10.1124/jpet.122.001415
DO - 10.1124/jpet.122.001415
M3 - Article
C2 - 37105582
AN - SCOPUS:85165222156
SN - 0022-3565
VL - 386
SP - 198
EP - 204
JO - Journal of Pharmacology and Experimental Therapeutics
JF - Journal of Pharmacology and Experimental Therapeutics
IS - 2
ER -