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A ROLE FOR REGULATORY T CELLS IN MATERNO-FETAL TOLERANCE?

Published online by Cambridge University Press:  13 January 2005

LAURE M DUSSABLY
Affiliation:
MRC Center for Immune Regulation, Institute of Biomedical Research, University of Birmingham, Birmingham, United Kingdom
DAVID A SOMERSET
Affiliation:
Department of Fetal Medicine, Division of Reproductive and Child Health, University of Birmingham, Birmingham Women's Hospital, Birmingham, United Kingdom
MARK D KILBY
Affiliation:
Department of Fetal Medicine, Division of Reproductive and Child Health, University of Birmingham, Birmingham Women's Hospital, Birmingham, United Kingdom
DAVID M SANSOM
Affiliation:
MRC Center for Immune Regulation, Institute of Biomedical Research, University of Birmingham, Birmingham, United Kingdom

Extract

Since the discovery that major histocompatibility complex (MHC) proteins provide a barrier to tissue transplantation between individuals it has been a paradox that, during pregnancy, the mother is able to retain a fetus that expresses MHC antigens from the father without rejection. The nature of this materno-fetal tolerance is not well understood and may involve multiple mechanisms. However since a major mechanism of histo-incompatible tissue rejection involves T lymphocytes, it seems plausible that controlling T cell responses is likely to be important. Recently, there has been considerable research activity focusing on the role of a sub-set of CD4+ T cells that express the interleukin-2 receptor chain CD25+. These CD4+CD25+ cells are termed regulatory T cells (Treg) based on their ability to prevent autoimmune tissue damage. In this review we discuss recent evidence that may link Treg to materno-fetal tolerance during pregnancy.

Type
Research Article
Copyright
© 2004 Cambridge University Press

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