Extinguishing maternal immune responses during pregnancy

Implications for immunosuppression

Andrew L. Mellor, David H. Munn

Research output: Contribution to journalArticle

59 Citations (Scopus)

Abstract

Mammals owe their existence to immunosuppressive processes that prevent fetal rejection in utero. Blocking tryptophan catabolism during murine pregnancy allows maternal T cells to provoke fetal allograft rejection. Cells expressing indoleamine 2,3-dioxygenase (IDO), which catabolizes tryptophan, prevent Tcell cycle progression and enhance activation induced T cell death. Here, we discuss the role of cells expressing IDO in regulating maternal T cell immunity during pregnancy and consider whether this mechanism might contribute to immunological discrimination by promoting T cell tolerance in other circumstances.

Original languageEnglish (US)
Pages (from-to)213-218
Number of pages6
JournalSeminars in Immunology
Volume13
Issue number4
DOIs
StatePublished - Jan 1 2001

Fingerprint

Immunosuppression
Mothers
Indoleamine-Pyrrole 2,3,-Dioxygenase
T-Lymphocytes
Pregnancy
Tryptophan
Immunosuppressive Agents
Allografts
Mammals
Immunity
Cell Death

Keywords

  • Fetal rejection
  • Immunosuppression
  • Maternal immune responses

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

Cite this

Extinguishing maternal immune responses during pregnancy : Implications for immunosuppression. / Mellor, Andrew L.; Munn, David H.

In: Seminars in Immunology, Vol. 13, No. 4, 01.01.2001, p. 213-218.

Research output: Contribution to journalArticle

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