Does the Presence or a High Titer of Yellow Fever Virus Antibodies Interfere with Pregnancy Outcomes in Women with Zika Virus Infection?

Author:

Piauilino Isa Cristina Ribeiro12,Souza Raillon Keven dos Santos2ORCID,Lima Maurício Teixeira3ORCID,Rodrigues Yanka Karolinna Batista12,da Silva Luís Felipe Alho12,Gouveia Ayrton Sena4,Neto Alexandre Vilhena da Silva12,Chaves Bárbara Aparecida2ORCID,Alecrim Maria das Graças Costa125,de Menezes Camila Helena Aguiar Bôtto12ORCID,Castilho Márcia da Costa2,Baia-da-Silva Djane Clarys1267,Espinosa Flor Ernestina Martinez127ORCID

Affiliation:

1. Programa de Pós-Graduação em Medicina Tropical (PPGMT), Universidade do Estado do Amazonas (UEA), Manaus 6904-000, Brazil

2. Fundação de Medicina Tropical Doutor Heitor Vieira Dourado, Manaus 6904-000, Brazil

3. Fundação Ezequiel Dias, Belo Horizonte 30510-010, Brazil

4. Programa de Pós-graduação em Biologia Parasitária, Instituto Oswaldo Cruz, Rio de Janeiro 21040-360, Brazil

5. Coordenação do Curso de Medicina da Faculdade Metropolitana de Manaus/FAMETRO, Manaus 69050-000, Brazil

6. Faculdade de Farmácia, Universidade Nilton Lins, Manaus 69058-030, Brazil

7. Instituto Leônidas & Maria Deane,-ILMD/FIOCRUZ Amazônia, Manaus 69057-070, Brazil

Abstract

Zika virus (ZIKV) and yellow fever virus (YFV) originated in Africa and expanded to the Americas, where both are co-circulated. It is hypothesized that in areas of high circulation and vaccination coverage against YFV, children of pregnant women have a lower risk of microcephaly. We evaluated the presence and titers of antibodies and outcomes in women who had ZIKV infection during pregnancy. Pregnancy outcomes were classified as severe, moderate, and without any important outcome. An outcome was defined as severe if miscarriage, stillbirth, or microcephaly occurred, and moderate if low birth weight and/or preterm delivery occurred. If none of these events were identified, the pregnancy was defined as having no adverse effects. A sample of 172 pregnant women with an acute ZIKV infection confirmed during pregnancy were collected throughout 2016. About 89% (150 of 169) of them presented immunity against YFV, including 100% (09 of 09) of those who had severe outcomes, 84% (16 of 19) of those who had moderate outcomes, and 89% (125 of 141) of those who had non-outcomes. There was no difference between groups regarding the presence of anti-YFV antibodies (p = 0.65) and YFV titers (p = 0.6). We were unable to demonstrate a protective association between the presence or titers of YFV antibodies and protection against serious adverse outcomes from exposure to ZIKV in utero.

Funder

Tropical Medicine Foundation Dr Heitor Vieira Dourado

Leônidas and Maria Deane Institute

Fundação para o Desenvolvimento Científico e Tecnológico em Saúde

Fundação de Amparo à Pesquisa do Estado do Amazonas

Ministry of Health of Brazil and Departamento de Ciência e Tecnologia

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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