Establishing Correlates of Maternal-Fetal Cytomegalovirus Transmission—One Step Closer Through Predictive Modeling

Author:

Marchant Arnaud1,Adali Sancar2ORCID,Alsdurf Hannah2,Bol Vanesa3,Capelle Xavier4,De Schrevel Nathalie3,Delroisse Jean-Marc5,Devlieger Roland67,Dieussaert Ilse3,Donner Catherine8,Janssens Michel3,Loquet Philip7,Panackal Anil A2,Seidl Claudia9,van den Berg Robert A2,Paris Robert2

Affiliation:

1. European Plotkin Institute for Vaccinology, Université libre de Bruxelles , Brussels , Belgium

2. GSK , Rockville, Maryland , USA

3. GSK , Rixensart , Belgium

4. Domaine Universitaire du Sart-Tilman, Service de Gynécologie-Obstétrique, Centre Hospitalier Universitaire de Liège , Belgium

5. GSK , Wavre, Belgium

6. Department of Obstetrics and Gynecology, University Hospitals KU Leuven , Belgium

7. Department of Obstetrics and Gynecology, GZA Ziekenhuizen–Campus Sint-Augustinus , Wilrijk , Belgium

8. Department of Obstetrics and Gynecology, Hôpital Erasme , Brussels , Belgium

9. GSK , Munich , Germany

Abstract

Abstract Background Determinants of maternal-fetal cytomegalovirus (CMV) transmission and factors influencing the severity of congenital CMV (cCMV) infection are not well understood. Methods We conducted a descriptive, multicenter study in pregnant women ≥18 years old with primary CMV infection and their newborns to explore maternal immune responses to CMV and determine potential immunologic/virologic correlates of cCMV following primary infection during pregnancy. We developed alternative approaches looking into univariate/multivariate factors associated with cCMV, including a participant clustering/stratification approach and an interpretable predictive model–based approach using trained decision trees for risk prediction (post hoc analyses). Results Pregnant women were grouped in 3 distinct clusters with similar baseline characteristics, particularly gestational age at diagnosis. We observed a trend for higher viral loads in urine and saliva samples from mothers of infants with cCMV versus without cCMV. When using a trained predictive-model approach that accounts for interaction effects between variables, anti-pentamer immunoglobulin G antibody concentration and viral load in saliva were identified as biomarkers jointly associated with the risk of maternal-fetal CMV transmission. Conclusions We identified biomarkers of CMV maternal-fetal transmission. After validation in larger studies, our findings will guide the management of primary infection during pregnancy and the development of vaccines against cCMV. Clinical Trials Registration NCT01251744.

Funder

GlaxoSmithKline Biologicals SA

Publisher

Oxford University Press (OUP)

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