Genotoxic signature in cord blood cells of newborns exposed in utero to a Zidovudine-based antiretroviral combination.

نویسندگان

  • Isabelle André-Schmutz
  • Liliane Dal-Cortivo
  • Emmanuelle Six
  • Sophie Kaltenbach
  • Fabienne Cocchiarella
  • Jerome Le Chenadec
  • Nicolas Cagnard
  • Anne-Gael Cordier
  • Alexandra Benachi
  • Laurent Mandelbrot
  • Elie Azria
  • Naima Bouallag
  • Sonia Luce
  • Brigitte Ternaux
  • Christian Reimann
  • Patrick Revy
  • Isabelle Radford-Weiss
  • Cristina Leschi
  • Alessandra Recchia
  • Fulvio Mavilio
  • Marina Cavazzana
  • Stéphane Blanche
چکیده

BACKGROUND The genotoxicity of zidovudine has been established in experimental models. The objective of the study was to identify genotoxicity markers in cord blood cells from newborns exposed in utero to antiretroviral (ARV) combinations containing zidovudine. METHODS Cells were investigated by karyotyping and gene expression analysis of the CD34(+) hematopoietic stem/progenitor cell (HPC) compartment. RESULTS Karyotyping of the cord blood cells from 15 ARV-exposed newborns and 12 controls revealed a higher proportion of aneuploid cells in the exposed group (median, 18.8% [interquartile range, 10.0%-26.7%] vs 6.6% [interquartile range, 3.1%-11.7%]; P < .001). All chromosomes were involved, with a random distribution of these alterations. Gene expression profiling of CD34(+) HPCs from 7 ARV-exposed and 6 control newborns revealed that >300 genes were significantly upregulated or downregulated by at least 1.5-fold in the exposed group (P < .05 for all comparisons). Significant alterations of genes involved in cell cycle control, mitotic checkpoints, and DNA repair were identified. Although this study does not allow discrimination between the roles of each of the 3 drugs, both cytogenetic and transcriptional findings are similar to those in cellular experiments that used zidovudine alone. CONCLUSIONS The cord blood cells, including hematopoietic stem cells, from newborns exposed in utero to a zidovudine-based ARV combination present cytogenetic and transcriptional abnormalities compatible with DNA damage.

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عنوان ژورنال:
  • The Journal of infectious diseases

دوره 208 2  شماره 

صفحات  -

تاریخ انتشار 2013