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Transfer of Respiratory Syncytial Virus Prefusion F Protein Antibody in Low Birthweight Infants.
Kachikis, Alisa B; Rumfelt, Kalee; Pike, Mindy; Sosa, Monica; Stolarczuk, Jennifer E; Cho, Hye; Eckert, Linda O; Martin, Emily T; Englund, Janet A.
Affiliation
  • Kachikis AB; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, USA.
  • Rumfelt K; Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, Michigan, USA.
  • Pike M; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, USA.
  • Sosa M; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, USA.
  • Stolarczuk JE; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, USA.
  • Cho H; School of Medicine, SUNY Upstate Medical University, Syracuse, New York, USA.
  • Eckert LO; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, USA.
  • Martin ET; Department of Global Health, University of Washington, Seattle, Washington, USA.
  • Englund JA; Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, Michigan, USA.
Open Forum Infect Dis ; 11(7): ofae314, 2024 Jul.
Article in En | MEDLINE | ID: mdl-39040482
ABSTRACT

Background:

Respiratory syncytial virus (RSV)-associated lower respiratory tract infection contributes significantly to morbidity/mortality worldwide in low birthweight (LBW) infants (<2500 g). Studies have demonstrated decreased maternal immunoglobulin G (IgG) transfer of various antibodies to LBW infants. We aimed to evaluate naturally acquired RSV anti-prefusion F protein (anti-preF) antibody transfer in pregnancies with LBW versus normal birthweight (NBW) infants.

Methods:

In this cohort study conducted among pregnant individuals and their infants, we tested paired maternal and singleton infant cord samples for RSV anti-preF IgG via an electrochemiluminescence immunoassay, using linear regression to evaluate associations between LBW and anti-preF IgG. Covariates included seasonality, insurance, small-for-gestational-age birthweight, and gestational age at delivery.

Results:

We tested maternal/cord RSV anti-preF IgG from 54 and 110 pregnancies with LBW and NBW infants, respectively. Of LBW infants, 22 (40.7%) were born both preterm and with small-for-gestational-age birthweight. The median (interquartile range) gestational age at delivery and birthweight were 34.0 (31.7-37.1) weeks and 1902 (1393-2276) g for LBW infants versus 39.1 (38.3-39.9) weeks and 3323 (3109-3565) g for NBW infants (both P < .001). In unadjusted comparisons, preterm infants had significantly lower cord anti-preF IgG levels and cord-maternal IgG ratios compared with full-term infants, while LBW infants had significantly lower cord-maternal IgG ratios than NBW infants (all P < .01). After adjustment for covariates, there was no difference in cord-maternal IgG ratios (ß =-0.29 [95% confidence interval, -.63 to .05]) between LBW and NBW infants.

Conclusions:

We documented robust transfer of maternal RSV anti-preF IgG in pregnancies with both LBW and NBW infants. Further studies are needed to assess immune protection in at-risk infants.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Open Forum Infect Dis Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Open Forum Infect Dis Year: 2024 Document type: Article