Legacy and emerging per- and polyfluoroalkyl substances suppress the neutrophil respiratory burst

Per- and polyfluoroalkyl substances (PFASs) are used in a multitude of processes and products, including nonstick coatings, food wrappers, and fire-fighting foams. These chemicals are environmentally-persistent, ubiquitous, and can be detected in the serum of 98% of Americans. Despite evidence that...

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Published inJournal of immunotoxicology Vol. 20; no. 1; p. 2176953
Main Authors Phelps, Drake W., Palekar, Anika I., Conley, Haleigh E., Ferrero, Giuliano, Driggers, Jacob H., Linder, Keith E., Kullman, Seth W., Reif, David M., Sheats, M. Katie, DeWitt, Jamie C., Yoder, Jeffrey A.
Format Journal Article
LanguageEnglish
Published England Taylor & Francis 01.12.2023
Taylor & Francis Ltd
Taylor & Francis Group
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Summary:Per- and polyfluoroalkyl substances (PFASs) are used in a multitude of processes and products, including nonstick coatings, food wrappers, and fire-fighting foams. These chemicals are environmentally-persistent, ubiquitous, and can be detected in the serum of 98% of Americans. Despite evidence that PFASs alter adaptive immunity, few studies have investigated their effects on innate immunity. The report here presents results of studies that investigated the impact of nine environmentally-relevant PFASs [e.g. perfluorooctanoic acid (PFOA), perfluorooctane sulfonic acid potassium salt (PFOS-K), perfluorononanoic acid (PFNA), perfluorohexanoic acid (PFHxA), perfluorohexane sulfonic acid (PFHxS), perfluorobutane sulfonic acid (PFBS), ammonium perfluoro(2-methyl-3-oxahexanoate) (GenX), 7H-perfluoro-4-methyl-3,6-dioxa-octane sulfonic acid (Nafion byproduct 2), and perfluoromethoxyacetic acid sodium salt (PFMOAA-Na)] on one component of the innate immune response, the neutrophil respiratory burst. The respiratory burst is a key innate immune process by which microbicidal reactive oxygen species (ROS) are rapidly induced by neutrophils in response to pathogens; defects in the respiratory burst can increase susceptibility to infection. The study here utilized larval zebrafish, a human neutrophil-like cell line, and primary human neutrophils to ascertain whether PFAS exposure inhibits ROS production in the respiratory burst. It was observed that exposure to PFHxA and GenX suppresses the respiratory burst in zebrafish larvae and a human neutrophil-like cell line. GenX also suppressed the respiratory burst in primary human neutrophils. This report is the first to demonstrate that these PFASs suppress neutrophil function and support the utility of employing zebrafish larvae and a human cell line as screening tools to identify chemicals that may suppress human immune function.
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Author Contributions
DWP and JAY contributed to study conception. DWP, MKS, SWK, JCD and JAY contributed to study design. Material preparation and data collection were performed by DWP, AIP, HEC, GF, JHD, KEL and MKS. Data analyses were performed by DWP and DMR aided in statistical analysis. The first manuscript draft was written by DWP. All authors commented on previous versions of the manuscript, and read and approved the final manuscript. SWK, JCD, MKS and JAY secured funding for this study. JAY supervised the completion of the project.
ISSN:1547-691X
1547-6901
1547-6901
DOI:10.1080/1547691X.2023.2176953