TY - JOUR
T1 - Cross-sectional associations of maternal PFAS exposure on SARS-CoV-2 IgG antibody levels during pregnancy
AU - Kaur, Kirtan
AU - Lesseur, Corina
AU - Chen, Lixian
AU - Andra, Syam S.
AU - Narasimhan, Srinivasan
AU - Pulivarthi, Divya
AU - Midya, Vishal
AU - Ma, Yula
AU - Ibroci, Erona
AU - Gigase, Frederieke
AU - Lieber, Molly
AU - Lieb, Whitney
AU - Janevic, Teresa
AU - De Witte, Lotje D.
AU - Bergink, Veerle
AU - Rommel, Anna Sophie
AU - Chen, Jia
N1 - Funding Information:
The authors thank the Gen C team, especially Sophie Orn, for collecting and processing biospecimens; Dr. Florian Krammer and his laboratory members for the COVID-19 antibody assay and results; the Chen lab members for their lab support and data feedback (Drs. James Wetmur, Hachem Saddiki and Qian Li); the HHEARS's program manager; Tracy Spangler for assisting in the application process; and the CDC's COVID-19 response and epidemiology task force and Pregnancy and Infant Linked Outcomes Team (PILOT).
Funding Information:
This project was partially supported by the CDC (BAA 75D30120C08186) for the Gen C study. The NIEHS Human Health Exposure Analysis Resource (HHEAR) NIH 2U2CES026561 funded the PFAS measurements, which were carried out within the Senator Frank R. Lautenberg Environmental Health Sciences Laboratory at the Icahn School of Medicine at Mount Sinai. The NIEHS T32HD049311 funded K. Kaur.
Publisher Copyright:
© 2022
PY - 2023/2/15
Y1 - 2023/2/15
N2 - Background: Perfluoroalkylated substances (PFAS) are man-made, persistent organic compounds with immune-modulating potentials. Given that pregnancy itself represents an altered state of immunity, PFAS exposure-related immunotoxicity is an important environmental factor to consider in SARS-CoV-2 infection during pregnancy as it may further affect humoral immune responses. Aim: To investigate the relationship between maternal plasma PFAS concentrations and SARS-CoV-2 antibody levels in a NYC-based pregnancy cohort. Methods: Maternal plasma was collected from 72 SARS-CoV-2 IgG + participants of the Generation C Study, a birth cohort established at the beginning of the COVID-19 pandemic in New York City. Maternal SARS-CoV-2 anti-spike IgG antibody levels were measured using ELISA. A panel of 16 PFAS congeners were measured in maternal plasma using a targeted UHPLC-MS/MS-based assay. Spearman correlations and linear regressions were employed to explore associations between maternal IgG antibody levels and plasma PFAS concentrations. Weighted quantile sum (WQS) regression was also used to evaluate mixture effects of PFAS. Models were adjusted for maternal age, gestational age at which SARS-CoV-2 IgG titer was measured, COVID-19 vaccination status prior to IgG titer measurement, maternal race/ethnicity, parity, type of insurance and pre-pregnancy BMI. Results: Our study population is ethnically diverse with an average maternal age of 32 years. Of the 16 PFAS congeners measured, nine were detected in more than 60% samples. Importantly, all nine congeners were negatively correlated with SARS-CoV-2 anti-spike IgG antibody levels; n-PFOA and PFHxS, PFHpS, and PFHxA reached statistical significance (p < 0.05) in multivariable analyses. When we examined the mixture effects using WQS, a quartile increase in the PFAS mixture-index was significantly associated with lower maternal IgG antibody titers (beta [95% CI] = −0.35 [-0.52, −0.17]). PFHxA was the top contributor to the overall mixture effect. Conclusions: Our study results support the notion that PFAS, including short-chain emerging PFAS, act as immunosuppressants during pregnancy. Whether such compromised immune activity leads to downstream health effects, such as the severity of COVID-19 symptoms, adverse obstetric outcomes or neonatal immune responses remains to be investigated.
AB - Background: Perfluoroalkylated substances (PFAS) are man-made, persistent organic compounds with immune-modulating potentials. Given that pregnancy itself represents an altered state of immunity, PFAS exposure-related immunotoxicity is an important environmental factor to consider in SARS-CoV-2 infection during pregnancy as it may further affect humoral immune responses. Aim: To investigate the relationship between maternal plasma PFAS concentrations and SARS-CoV-2 antibody levels in a NYC-based pregnancy cohort. Methods: Maternal plasma was collected from 72 SARS-CoV-2 IgG + participants of the Generation C Study, a birth cohort established at the beginning of the COVID-19 pandemic in New York City. Maternal SARS-CoV-2 anti-spike IgG antibody levels were measured using ELISA. A panel of 16 PFAS congeners were measured in maternal plasma using a targeted UHPLC-MS/MS-based assay. Spearman correlations and linear regressions were employed to explore associations between maternal IgG antibody levels and plasma PFAS concentrations. Weighted quantile sum (WQS) regression was also used to evaluate mixture effects of PFAS. Models were adjusted for maternal age, gestational age at which SARS-CoV-2 IgG titer was measured, COVID-19 vaccination status prior to IgG titer measurement, maternal race/ethnicity, parity, type of insurance and pre-pregnancy BMI. Results: Our study population is ethnically diverse with an average maternal age of 32 years. Of the 16 PFAS congeners measured, nine were detected in more than 60% samples. Importantly, all nine congeners were negatively correlated with SARS-CoV-2 anti-spike IgG antibody levels; n-PFOA and PFHxS, PFHpS, and PFHxA reached statistical significance (p < 0.05) in multivariable analyses. When we examined the mixture effects using WQS, a quartile increase in the PFAS mixture-index was significantly associated with lower maternal IgG antibody titers (beta [95% CI] = −0.35 [-0.52, −0.17]). PFHxA was the top contributor to the overall mixture effect. Conclusions: Our study results support the notion that PFAS, including short-chain emerging PFAS, act as immunosuppressants during pregnancy. Whether such compromised immune activity leads to downstream health effects, such as the severity of COVID-19 symptoms, adverse obstetric outcomes or neonatal immune responses remains to be investigated.
KW - COVID19
KW - Immunotoxicity
KW - PFAS
KW - Pregnancy
KW - SARS-CoV-2 IgG
UR - http://www.scopus.com/inward/record.url?scp=85144283800&partnerID=8YFLogxK
U2 - 10.1016/j.envres.2022.115067
DO - 10.1016/j.envres.2022.115067
M3 - Article
C2 - 36528042
AN - SCOPUS:85144283800
SN - 0013-9351
VL - 219
JO - Environmental Research
JF - Environmental Research
M1 - 115067
ER -