ZIKA Virus Neutralizing Antibody Kinetics in Antenatally Exposed Infants

Author:

Espindola Otavio de Melo1,Jaenisch Thomas2345,Nielsen-Saines Karin6,Oliveira Raquel de Vasconcellos Carvalhaes de1,Pastorino Boris7,Vasconcelos Zilton8,Gabaglia Claudia Raja9,Ribeiro Ieda Pereira10,Cunha Denise Cotrim da11,Pone Marcos Vinicius8,Carvalho Liege Maria Abreu de8,Pone Sheila Moura8,Damasceno Luana1,Zin Andrea Araujo8,Bonaldo Myrna C10,Moreira Maria Elisabeth Lopes8,Cherry James D6,de Lamballerie Xavier7,Brasil Patrícia1

Affiliation:

1. Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil

2. Heidelberg Institute of Global Health, Heidelberg University Hospital, Heidelberg, Germany

3. Section Clinical Tropical Medicine, Department of Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany

4. Center for Global Health, Colorado School of Public Health, Aurora, USA

5. Pediatric Infectious Diseases, Colorado School of Medicine, Aurora, USA

6. David Geffen School of Medicine, University of California at Los Angeles, California, USA

7. Unité des Virus Émergents, Aix-Marseille Université, IRD 190 Inserm 1207, IHU Méditerranée Infection, Marseille, France

8. Instituto Fernandes Figueira, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil

9. Biomedical Research Institute of Southern California, Oceanside, California, USA

10. Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil

11. Escola Nacional de Saúde Pública Sérgio Arouca, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil

Abstract

Abstract Background Zika virus (ZIKV) is associated with severe congenital abnormalities and laboratory diagnosis of antenatal infection is difficult. Here we evaluated ZIKV neutralizing antibody (nAb) kinetics in infants born to mothers with PCR-confirmed ZIKV infection during pregnancy. Methods Neonates (n = 98) had serum specimens tested repeatedly for ZIKV nAb over the first 2 years of life using virus neutralization test (VNT). ZIKV neonatal infection was confirmed by RT-PCR in blood or urine and/or presence of ZIKV IgM antibodies, and results were correlated with infant clinical features. Results Postnatal laboratory evidence of ZIKV vertical transmission was obtained for 60.2% of children, while 32.7% exhibited clinical abnormalities. Congenital abnormalities were found in 37.3% of children with confirmed ZIKV infection and 31.0% of children without confirmed infection (P = .734). All but 1 child displayed a physiologic decline in ZIKV nAb, reflecting maternal antibody decay, despite an early ZIKV-IgM response in one-third of infants. Conclusions Infants with antenatal ZIKV exposure do not develop ZIKV nAb despite an early IgM response. Therefore, ZIKV VNT in children is not useful for diagnosis of congenital infection. In light of these findings, it remains to be determined if children infected in utero are potentially susceptible to reinfection.

Funder

Department of Science and Technology, Brazilian Ministry of Health

Coordination for the Improvement of Higher Level or Education Personnel

Brazilian National Council for Scientific and Technological Development

Fundação Carlos Chagas de Amparo à Pesquisa do Estado do Rio de Janeiro

Thrasher Research Fund

European Union Horizon 2020 Research and Innovation Programme

National Institute of Allergy and Infectious Diseases

National Institutes of Health

National Eye Institute

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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