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The objective of this study was to investigate the effect of IUGR during late pregnancy on the development of the ovine fetal thymus and the T\u2010lymphocyte subpopulation.<\/jats:p><\/jats:sec><jats:sec><jats:title>Method of study<\/jats:title><jats:p>Eighteen time\u2010mated ewes with singleton fetuses were allocated to three groups at day 90 of pregnancy: restricted group 1 (<jats:styled-content style=\"fixed-case\">RG<\/jats:styled-content>1, 0.18 <jats:styled-content style=\"fixed-case\">MJ ME<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">BW<\/jats:styled-content><jats:sup>0.75<\/jats:sup>\/day, <jats:italic>n<\/jats:italic>\u00a0=\u00a06), restricted group 2 (<jats:styled-content style=\"fixed-case\">RG<\/jats:styled-content>2, 0.33 <jats:styled-content style=\"fixed-case\">MJ ME<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">BW<\/jats:styled-content><jats:sup>0.75<\/jats:sup>\/day, <jats:italic>n<\/jats:italic>\u00a0=\u00a06) and a control group (<jats:styled-content style=\"fixed-case\">CG<\/jats:styled-content>,<jats:italic> ad libitum<\/jats:italic>, 0.67 <jats:styled-content style=\"fixed-case\">MJ ME<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">BW<\/jats:styled-content><jats:sup>0.75<\/jats:sup>\/day, <jats:italic>n<\/jats:italic>\u00a0=\u00a06). Fetuses were recovered at slaughter on day 140.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Fetuses in <jats:styled-content style=\"fixed-case\">RG<\/jats:styled-content>1 exhibited decreased (<jats:italic>P\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.05) thymic weight, cortical thickness, cortical:medullary, <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> content, total antioxidant capacity, and superoxide dismutase; intermediate changes were found in <jats:styled-content style=\"fixed-case\">RG<\/jats:styled-content>2 fetuses, including decreased thymic weight, cortical thickness, and <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> content (<jats:italic>P\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.05). The reductions (<jats:italic>P\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.05) of <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup>T cells, relative <jats:styled-content style=\"fixed-case\">mRNA<\/jats:styled-content> expression of <jats:italic>keratin 8<\/jats:italic>,<jats:italic> recombination activating gene 1<\/jats:italic> (<jats:italic><jats:styled-content style=\"fixed-case\">RAG<\/jats:styled-content>1<\/jats:italic>), and <jats:italic>B\u2010cell lymphoma 2<\/jats:italic> (<jats:italic>Bcl\u20102<\/jats:italic>) were found in both restricted groups. In addition, there was reduced <jats:styled-content style=\"fixed-case\">mRNA<\/jats:styled-content> expression (<jats:italic>P\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.05) of <jats:italic>T\u2010cell receptor<\/jats:italic>,<jats:italic> apoptosis antigen 1 ligand<\/jats:italic>, and <jats:italic><jats:styled-content style=\"fixed-case\">RAG<\/jats:styled-content>2<\/jats:italic> in the <jats:styled-content style=\"fixed-case\">RG<\/jats:styled-content>1 group. In contrast, increases in glutathione peroxidase, malondialdehyde, caspase\u20103, Cytochrome <jats:italic>c<\/jats:italic>, and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup>T cells were observed (<jats:italic>P\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.05), and higher <jats:styled-content style=\"fixed-case\">mRNA<\/jats:styled-content> expressions (<jats:italic>P\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.05) of <jats:italic>protein 53<\/jats:italic>,<jats:italic> Bcl\u20102 associated X protein<\/jats:italic> (<jats:italic>Bax<\/jats:italic>), and <jats:italic>apoptosis antigen 1<\/jats:italic> (<jats:italic>Fas<\/jats:italic>) were found in <jats:styled-content style=\"fixed-case\">RG<\/jats:styled-content>1 fetuses; and thymuses of <jats:styled-content style=\"fixed-case\">RG<\/jats:styled-content>2 fetuses had increased caspase\u20103, and expression of <jats:italic>Fas<\/jats:italic> and <jats:italic>Bax<\/jats:italic> (<jats:italic>P\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.05), relative to control fetuses.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>These results indicate that reduced cell proliferation, oxidative stress, and increased cell apoptosis were the potential mechanisms for impaired development and microenvironment of <jats:styled-content style=\"fixed-case\">IUGR<\/jats:styled-content> fetal thymus, and for modifying the maturation of <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup> thymocytes underlying their reduced numbers 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