Neonatal protection and preterm birth reduction following maternal group B streptococcus vaccination in a mouse model

R. Bernardini, R Aufieri, Antoaneta Detcheva, S. Recchia, R. Cicconi, Massimo Amicosante, C. Montesano, P Rossi, Hyppolite K. Tchidjou, Bogdan Petrunov, G. Orefici, M. Mattei

Research output: Contribution to journalArticle

Abstract

PURPOSE: Evaluate effects of maternal immunization in a mouse model of Group B Streptococcus (GBS) vaginal colonization using clinical isolates.

MATERIALS AND METHODS: Female pregnant mice were immunized with heat-killed GBS 21 days before pregnancy and were inoculated intravaginally with GBS cultures (5 × 10(7) CFU twice a day for three days) from the 16th day of pregnancy. Gestation period and mice survival were monitored. Maternal anti-GBS IgG levels have been determined by ELISA analysis in vaccinated, unvaccinated mothers and newborns.

RESULTS: Maternal immunization before pregnancy provided protection to newborns for three of the four GBS strains used. Evaluation of the immunogenicity showed that this vaccination induced higher levels of IgG in vaccinated compared to unvaccinated dams and the presence of antibodies in the offspring at embryonic and postnatal age, and a Th1 response and high levels of IgG2a subclass antibody and IFN-γ were detected. A significant reduction of preterm births was observed in vaccinated mothers (p< 0.05).

CONCLUSIONS: Our finding suggest that vaccinated mothers could protect their progeny from GBS infection and preterm birth through passive immunization. The proposed mouse model may represent a noninvasive and effective tool to investigate pathogenetic mechanisms of GBS ascending infection and for vaccine protection studies.

Original languageEnglish
Pages (from-to)1-7
Number of pages7
JournalJournal of Maternal-Fetal and Neonatal Medicine
DOIs
Publication statusE-pub ahead of print - Dec 14 2016

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Streptococcus agalactiae
Premature Birth
Vaccination
Mothers
Pregnancy
Immunization
Immunoglobulin G
Passive Immunization
Antibodies
Infection
Vaccines
Hot Temperature
Enzyme-Linked Immunosorbent Assay

Keywords

  • Journal Article

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Neonatal protection and preterm birth reduction following maternal group B streptococcus vaccination in a mouse model. / Bernardini, R.; Aufieri, R; Detcheva, Antoaneta; Recchia, S.; Cicconi, R.; Amicosante, Massimo; Montesano, C.; Rossi, P; Tchidjou, Hyppolite K.; Petrunov, Bogdan; Orefici, G.; Mattei, M.

In: Journal of Maternal-Fetal and Neonatal Medicine, 14.12.2016, p. 1-7.

Research output: Contribution to journalArticle

Bernardini, R, Aufieri, R, Detcheva, A, Recchia, S, Cicconi, R, Amicosante, M, Montesano, C, Rossi, P, Tchidjou, HK, Petrunov, B, Orefici, G & Mattei, M 2016, 'Neonatal protection and preterm birth reduction following maternal group B streptococcus vaccination in a mouse model', Journal of Maternal-Fetal and Neonatal Medicine, pp. 1-7. https://doi.org/10.1080/14767058.2016.1265932
Bernardini, R. ; Aufieri, R ; Detcheva, Antoaneta ; Recchia, S. ; Cicconi, R. ; Amicosante, Massimo ; Montesano, C. ; Rossi, P ; Tchidjou, Hyppolite K. ; Petrunov, Bogdan ; Orefici, G. ; Mattei, M. / Neonatal protection and preterm birth reduction following maternal group B streptococcus vaccination in a mouse model. In: Journal of Maternal-Fetal and Neonatal Medicine. 2016 ; pp. 1-7.
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AU - Cicconi, R.

AU - Amicosante, Massimo

AU - Montesano, C.

AU - Rossi, P

AU - Tchidjou, Hyppolite K.

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AU - Orefici, G.

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AB - PURPOSE: Evaluate effects of maternal immunization in a mouse model of Group B Streptococcus (GBS) vaginal colonization using clinical isolates.MATERIALS AND METHODS: Female pregnant mice were immunized with heat-killed GBS 21 days before pregnancy and were inoculated intravaginally with GBS cultures (5 × 10(7) CFU twice a day for three days) from the 16th day of pregnancy. Gestation period and mice survival were monitored. Maternal anti-GBS IgG levels have been determined by ELISA analysis in vaccinated, unvaccinated mothers and newborns.RESULTS: Maternal immunization before pregnancy provided protection to newborns for three of the four GBS strains used. Evaluation of the immunogenicity showed that this vaccination induced higher levels of IgG in vaccinated compared to unvaccinated dams and the presence of antibodies in the offspring at embryonic and postnatal age, and a Th1 response and high levels of IgG2a subclass antibody and IFN-γ were detected. A significant reduction of preterm births was observed in vaccinated mothers (p< 0.05).CONCLUSIONS: Our finding suggest that vaccinated mothers could protect their progeny from GBS infection and preterm birth through passive immunization. The proposed mouse model may represent a noninvasive and effective tool to investigate pathogenetic mechanisms of GBS ascending infection and for vaccine protection studies.

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