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DOI 10.1002/cti2.1082

Медицинская библиотека · Clinical & translational immunology · 2019

Immunological observations and transcriptomic analysis of trimester-specific full-term placentas from three Zika virus-infected women.

Lum Fok-Moon, Narang Vipin, Hue Susan, Chen Jie, McGovern Naomi, Rajarethinam Ravisankar, Tan Jeslin Jl, Amrun Siti Naqiah, Chan Yi-Hao, Lee Cheryl Yp, Chua Tze-Kwang, Yee Wearn-Xin, Yeo Nicholas Kw, Tan Thiam-Chye, Liu Xuan, Haldenby Sam, Leo Yee-Sin, Ginhoux Florent, Chan Jerry Ky, Hiscox Julian, Chong Chia-Yin, Ng Lisa Fp

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Аннотация

OBJECTIVES

Effects of Zika virus (ZIKV) infection on placental development during pregnancy are unclear.

METHODS

Full-term placentas from three women, each infected with ZIKV during specific pregnancy trimesters, were harvested for anatomic, immunologic and transcriptomic analysis.

RESULTS

In this study, each woman exhibited a unique immune response with raised IL-1RA, IP-10, EGF and RANTES expression and neutrophil numbers during the acute infection phase. Although ZIKV NS3 antigens co-localised to placental Hofbauer cells, the placentas showed no anatomic defects. Transcriptomic analysis of samples from the placentas revealed that infection during trimester 1 caused a disparate cellular response centred on differential eIF2 signalling, mitochondrial dysfunction and oxidative phosphorylation. Despite these, the babies were delivered without any congenital anomalies.

CONCLUSION

These findings should translate to improve clinical prenatal screening procedures for virus-infected pregnant patients.

Для цитирования: Lum Fok-Moon, Narang Vipin, Hue Susan, Chen Jie, McGovern Naomi, Rajarethinam Ravisankar, Tan Jeslin Jl, Amrun Siti Naqiah, Chan Yi-Hao, Lee Cheryl Yp, Chua Tze-Kwang, Yee Wearn-Xin, Yeo Nicholas Kw, Tan Thiam-Chye, Liu Xuan, Haldenby Sam, Leo Yee-Sin, Ginhoux Florent, Chan Jerry Ky, Hiscox Julian, Chong Chia-Yin, Ng Lisa Fp. Immunological observations and transcriptomic analysis of trimester-specific full-term placentas from three Zika virus-infected women.. Clinical & translational immunology. 2019. DOI: 10.1002/cti2.1082.
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