251. Regulatory T cells, maternal-foetal immune tolerance and recurrent miscarriage: new therapeutic challenging opportunities.
- Author
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Alijotas-Reig J, Melnychuk T, and Gris JM
- Subjects
- Abortion, Habitual therapy, Biomarkers metabolism, Female, Fetus immunology, Forkhead Transcription Factors metabolism, Humans, Pregnancy, Abortion, Habitual immunology, Immune Tolerance, Maternal-Fetal Exchange immunology, T-Lymphocytes, Regulatory metabolism
- Abstract
Because maternal alloreactive lymphocytes are not depleted during pregnancy, local and/or systemic mechanisms have to play a key role in altering the maternal immune response. Peripheral T regulatory cells (pTregs) at the maternal-foetal interface are necessary in situ to prevent early abortion, but only those pTregs that have been previously exposed to paternal alloantigens. It has been showed that pregnancy selectively stimulates the accumulation of maternal Foxp3(+)CD4(+)CD25(+) (Foxp3Tregs) cells with foetal specificity. Interestingly, after delivery, foetal-specific pTregs persist at elevated levels, maintain tolerance to pre-existing foetal antigen, and rapidly re-accumulate during subsequent pregnancy. pTreg up-regulation could be hypothesized as a possible future therapeutic strategy in humans., (Copyright © 2014 Elsevier España, S.L.U. All rights reserved.)
- Published
- 2015
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