Congenital human cytomegalovirus infection is associated with decreased transplacental IgG transfer efficiency due to maternal hypergammaglobulinemia.
| dc.contributor.author | Semmes, Eleanor C | |
| dc.contributor.author | Li, Shuk Hang | |
| dc.contributor.author | Hurst, Jillian H | |
| dc.contributor.author | Yang, Zidanyue | |
| dc.contributor.author | Niedzwiecki, Donna | |
| dc.contributor.author | Fouda, Genevieve G | |
| dc.contributor.author | Kurtzberg, Joanne | |
| dc.contributor.author | Walsh, Kyle M | |
| dc.contributor.author | Permar, Sallie R | |
| dc.date.accessioned | 2022-03-24T14:16:04Z | |
| dc.date.available | 2022-03-24T14:16:04Z | |
| dc.date.issued | 2021-07-14 | |
| dc.date.updated | 2022-03-24T14:16:03Z | |
| dc.description.abstract | BackgroundPlacentally-transferred maternal IgG protects against pathogens in early life, yet vertically-transmitted infections can interfere with transplacental IgG transfer. Although human cytomegalovirus (HCMV) is the most common placentally-transmitted viral infection worldwide, the impact of congenital HCMV (cCMV) infection on transplacental IgG transfer has been underexplored.MethodsWe evaluated total and antigen-specific maternal and cord blood IgG levels and transplacental IgG transfer efficiency in a U.S-based cohort of 93 mother-infant pairs including 27 cCMV-infected and 66 cCMV-uninfected pairs, of which 29 infants were born to HCMV-seropositive non-transmitting mothers and 37 to HCMV-seronegative mothers. Controls were matched on sex, race/ethnicity, maternal age, and delivery year.ResultsTransplacental IgG transfer efficiency was decreased by 23% (95% CI 10-36%, p=0.0079) in cCMV-infected pairs and 75% of this effect (95% CI 28-174%, p=0.0085) was mediated by elevated maternal IgG levels (i.e., hypergammaglobulinemia) in HCMV-transmitting women. Despite reduced transfer efficiency, IgG levels were similar in cord blood from infants with and without cCMV infection.ConclusionsOur results indicate that cCMV infection moderately reduces transplacental IgG transfer efficiency due to maternal hypergammaglobulinemia; however, infants with and without cCMV infection had similar antigen-specific IgG levels, suggesting comparable protection from maternal IgG acquired via transplacental transfer. | |
| dc.identifier | 6321289 | |
| dc.identifier.issn | 1058-4838 | |
| dc.identifier.issn | 1537-6591 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Oxford University Press (OUP) | |
| dc.relation.ispartof | Clinical infectious diseases : an official publication of the Infectious Diseases Society of America | |
| dc.relation.isversionof | 10.1093/cid/ciab627 | |
| dc.subject | congenital CMV infection | |
| dc.subject | human cytomegalovirus | |
| dc.subject | maternal hypergammaglobulinemia | |
| dc.subject | maternal-fetal vaccination | |
| dc.subject | transplacental IgG transfer | |
| dc.title | Congenital human cytomegalovirus infection is associated with decreased transplacental IgG transfer efficiency due to maternal hypergammaglobulinemia. | |
| dc.type | Journal article | |
| duke.contributor.orcid | Hurst, Jillian H|0000-0001-5079-9920 | |
| duke.contributor.orcid | Yang, Zidanyue|0000-0002-4843-4313 | |
| duke.contributor.orcid | Niedzwiecki, Donna|0000-0002-3566-0450 | |
| duke.contributor.orcid | Kurtzberg, Joanne|0000-0002-3370-0703 | |
| duke.contributor.orcid | Walsh, Kyle M|0000-0002-5879-9981 | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Staff | |
| pubs.organisational-group | Basic Science Departments | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | Biostatistics & Bioinformatics | |
| pubs.organisational-group | Pathology | |
| pubs.organisational-group | Pediatrics | |
| pubs.organisational-group | Psychiatry & Behavioral Sciences | |
| pubs.organisational-group | Duke Cancer Institute | |
| pubs.organisational-group | Institutes and Provost's Academic Units | |
| pubs.organisational-group | Initiatives | |
| pubs.organisational-group | Neurosurgery | |
| pubs.organisational-group | Population Health Sciences | |
| pubs.organisational-group | Duke Innovation & Entrepreneurship | |
| pubs.organisational-group | Pediatrics, Transplant and Cellular Therapy | |
| pubs.publication-status | Published |
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