Epidemiology and pathogenesis of maternal-fetal transmission of Trypanosoma cruzi and a case for vaccine development against congenital Chagas disease

Trypanos o ma cruzi (T. cruzi or Tc) is the causative agent of Chagas disease (CD). It is common for patients to suffer from non-specific symptoms or be clinically asymptomatic with acute and chronic conditions acquired through various routes of transmission. The expecting women and their fetuses ar...

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Veröffentlicht in:Biochimica et biophysica acta. Molecular basis of disease 2020-03, Vol.1866 (3), p.165591-165591, Article 165591
Hauptverfasser: Rios, Lizette, Campos, E. Emanuel, Menon, Ramkumar, Zago, M. Paola, Garg, Nisha J.
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Sprache:eng
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Zusammenfassung:Trypanos o ma cruzi (T. cruzi or Tc) is the causative agent of Chagas disease (CD). It is common for patients to suffer from non-specific symptoms or be clinically asymptomatic with acute and chronic conditions acquired through various routes of transmission. The expecting women and their fetuses are vulnerable to congenital transmission of Tc. Pregnant women face formidable health challenges because the frontline antiparasitic drugs, benznidazole and nifurtimox, are contraindicated during pregnancy. However, it is worthwhile to highlight that newborns can be cured if they are diagnosed and given treatment in a timely manner. In this review, we discuss the pathogenesis of maternal-fetal transmission of Tc and provide a justification for the investment in the development of vaccines against congenital CD. •Every year, several Trypanosoma cruzi-infected babies are born to infected mothers in endemic and non-endemic countries.•Mandatory prompt diagnosis and treatment of infected babies would have a positive clinical and epidemiological impact.•Knowledge of risk factors for maternal-fetal transmission would offer strategies for control of congenital Chagas disease.•Efforts to develop a vaccine that prevents vertical transmission of T. cruzi must be a public health priority.
ISSN:0925-4439
1879-260X
DOI:10.1016/j.bbadis.2019.165591