American Journal of Reproductive Immunology · 2007 · 39 citations · 29 references
Life SciencesImmunologyObstetricsMaternal-fetal MedicineObstetric ComplicationsReproductive ImmunologyMaternal-fetal Immune InteractionsPlacental BiologyPlacental ImmunologyPlacental PhysiologyPregnancy ImmunologyPregnancy PhysiologyBlood PressureEnzyme ActivityImmunological MechanismsIndoleamine 2, 3-Dioxygenase PathwayMaternal-fetal ImmunosuppressionPre-eclampsia ImmunopathologyPreeclampsia ImmunopathologyPreeclampsia Pathophysiology
PROBLEM: It has been demonstrated that allogeneic fetal rejection in normal pregnancy is prevented by placental indoleamine 2,3-dioxygenase (IDO). Further, an immunological etiology has been implicated in pre-eclampsia. METHOD OF STUDY: We examined the differences in placental IDO activity between normal and pre-eclamptic pregnancies. RESULTS: IDO mRNA expression and enzyme activity levels in the placenta were low in patients with severe pre-eclampsia. The enzyme activity also inversely correlates with the blood pressure of the patients. In the placentas from severe pre-eclampsia, IDO immunoreactivity was low, whereas regional T-cell infiltration was observed reciprocally proportional to the IDO activity. CONCLUSION: Our findings implicate a potential role for IDO activity and a maternal immunological reaction against an allogeneic fetus in the etiology of pre-eclampsia.
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Sharon E. Maynard, Jiang-Yong Min, Jaime R. Merchan et al. · Journal of Clinical Investigation · 2003 · 4K citations · Full text
Prevention of Allogeneic Fetal Rejection by Tryptophan Catabolism
David H. Munn, Min Zhou, John T. Attwood et al. · Science · 1998 · 2.6K citations
Inhibition of T Cell Proliferation by Macrophage Tryptophan Catabolism
David H. Munn, Ebrahim Shafizadeh, John T. Attwood et al. · The Journal of Experimental Medicine · 1999 · 1.6K citations · Full text
Mark Brown, Marshall D. Lindheimer, Michael de Swiet et al. · Hypertension in Pregnancy · 2001 · 1.4K citations · Full text
Medicine, Gynecology, Obstetrics +12