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Clostridioides difficile Immunity During Pregnancy and Passive Antibody Transfer to Neonates from Cord Blood and
Alban Le Monnier1,2,3, Claire de Curraize1,4, Valérie Seffer4
1Service de Biologie, Unité de Microbiologie, Centre Hospitalier de Versailles, 78150 Le Chesnay-Rocquencourt, France.
Insights
Maternal antibodies specific to Clostridioides difficile (C. difficile) are transferred to neonates via the placenta and breast milk, offering protection against C. difficile-associated disease. This study found no significant antibody boost in pregnant women with C. difficile infection.
Area of Science:
- Immunology
- Maternal-fetal medicine
- Microbiology
Background:
- Passive transplacental immunity is vital for protecting newborns from infections.
- Infants are colonized by Clostridioides difficile (C. difficile) but do not develop disease, suggesting protective mechanisms.
- Pregnant women face an increased risk of C. difficile infection (CDI).
Purpose of the Study:
- To characterize the humoral immune response specific to C. difficile toxins (TcdA, TcdB) and surface proteins (FliD, Cwp84) in pregnant women and their neonates.
- To investigate the transfer of C. difficile-specific antibodies from mother to neonate through the placenta and breast milk.
- To assess the antibody response in pregnant women diagnosed with CDI.
Main Methods:
- Quantitative ELISA was used to measure anti-C. difficile antibodies (IgG, IgA, IgM) in maternal serum, cord blood, and breast milk from 58 healthy pregnant women and their newborns.
- Sera from peripartum women with CDI were analyzed retrospectively.
- Antibody concentrations were correlated with maternal colonization status and compared between healthy pregnant women and those with CDI.
Main Results:
- High seroprevalence of IgG specific to C. difficile antigens was found in healthy pregnant women.
- A strong positive correlation between maternal and cord blood IgG levels indicated efficient transplacental transfer of C. difficile-specific antibodies.
- High IgA seroprevalence in breast milk and correlation with maternal serum levels suggested preferential transfer of specific IgG antibodies, providing a protective barrier.
Conclusions:
- Antibody-mediated maternal protection likely explains why neonates are protected from C. difficile-associated disease.
- Transplacental and breast milk transfer of C. difficile-specific antibodies are key mechanisms for neonatal immunity.
- Pregnant women with CDI did not show a significant boost in specific antibody concentrations, suggesting pre-existing immunity or other protective factors.
Abstract:
Passive transplacental immunity is crucial for neonatal protection from infections. Following Clostridioides difficile (C. difficile) infection, infants do not develop disease, although C. difficile colonization is highly prevalent in infants. This work aimed to characterize humoral immunity specific to C. difficile toxins TcdA and TcdB and to surface proteins FliD and Cwp84, well-known colonizing factors, in pregnant women and their neonates. Anti-C. difficile antibodies were measured in maternal serum, cord blood, and breast milk from 58 healthy pregnant women and their newborns, enrolled in a prospective study, using a quantitative ELISA. Anti-C. difficile antibodies were also measured in pregnant women with C. difficile infection (CDI) in a retrospective peripartum case series. We found a high seroprevalence of IgG specific to the four antigens in healthy pregnant women, regardless of colonization by C. difficile. However, pregnant women exhibited lower concentrations of TcdA-specific IgG antibodies compared to age-matched non-pregnant women. A strong positive correlation between maternal and cord blood IgG specific to TcdA, TcdB, FliD, and Cwp84 was observed, suggesting a transplacental transfer of C. difficile-specific IgG antibodies to neonates. In breast milk, a high seroprevalence of IgA specific to the two toxins was detected, and positive correlations between maternal serum and breast milk antibody levels highlight a preferential transfer of TcdB-specific IgG and Cwp84-specific IgG to breast milk, providing the infant with a protective barrier against C. difficile. Lastly, since pregnant women are at increased risk for C. difficile infection (CDI), we characterized the specific antibody response in a retrospective peripartum case series. Sera from peripartum women with CDI exhibited similar median concentrations of TcdA, TcdB, FliD, and Cwp84 IgM and IgG to those of healthy pregnant women. Moreover, except for one case, antibody concentrations remained stable during the longitudinal evolution of C. difficile response before and after diagnosis of CDI, without any booster effect. Altogether, these data are consistent with antibody-mediated maternal protection of neonates from C. difficile-associated disease. Larger studies exploring immune factors involved in protection from C. difficile-associated disease during pregnancy are needed.
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