A new study from Yale University shows that the same proteins that mount a potent immune response to Zika viral infection can also harm the placenta and fetal development. The study is published in Science Immunology.
Zika researchers had established that these antiviral proteins, known as type I interferons, were required to fight Zika infection in mothers. But it was not clear what role interferons played in providing an immune defense for the fetus.
To investigate, the team led by immunobiologist Akiko Iwasaki studied two different types of mouse models. One type lacked the receptor for type 1 interferon altogether, and the other had only one copy of the interferon receptor gene. Only the latter showed signs of abnormal placental development, restricted fetal growth and death, the researchers said.
The finding demonstrates that the damaging effects of the immune response to Zika virus can outweigh the benefits for fetuses, said the researchers, noting that although type 1 interferon is critical to blocking replication of the virus, too much of it can be detrimental during pregnancy. The study results may have implications for other infection-related pregnancy complications and possible interventions.
Other authors are Laura J. Yockey, Kellie A. Jurado, Nitin Arora, Alon Millet, Tasfia Rakib, Kristin M. Milano, Andrew K. Hastings, Erol Fikrig, Yong Kong, Tamas L. Horvath, Scott Weatherbee, Harvey J. Kliman, and Carolyn B. Coyne.
This study was supported in part by the National Institutes of Health.
Publication: Laura J. Yockey, et al., “Type I interferons instigate fetal demise after Zika virus infection,” Science Immunology 05 Jan 2018: Vol. 3, Issue 19, eaao1680; DOI: 10.1126/sciimmunol.aao1680