2015
DOI: 10.1016/j.ajog.2014.10.484
|View full text |Cite
|
Sign up to set email alerts
|

438: Disruption of maternal tolerance during pregnancy leads to treg repopulation of the antigenic UPI

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2017
2017
2017
2017

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 0 publications
0
1
0
Order By: Relevance
“…Tolerance is a specific immunological term that refers to “the active state of antigen‐specific non‐responsiveness” leading to diminished reactivity to paternal antigens expressed by the placenta and/or fetus; it is considered key for successful pregnancy . The mechanisms responsible for tolerance in pregnancy include the following: (i) T‐cell chemokine gene silencing in the decidual cells; (ii) a suppressive role of regulatory T cells; (iii) expression of non‐classical major histocompatibility complex molecules on trophoblast cells that do not elicit a maternal immune response; (iv) changes in tryptophan catabolisms; (v) T‐cell apoptosis; (vi) complement; and (vii) costimulatory molecules such as the programmed death ligand . Other mechanisms for tolerance are not currently understood.…”
Section: Introductionmentioning
confidence: 99%
“…Tolerance is a specific immunological term that refers to “the active state of antigen‐specific non‐responsiveness” leading to diminished reactivity to paternal antigens expressed by the placenta and/or fetus; it is considered key for successful pregnancy . The mechanisms responsible for tolerance in pregnancy include the following: (i) T‐cell chemokine gene silencing in the decidual cells; (ii) a suppressive role of regulatory T cells; (iii) expression of non‐classical major histocompatibility complex molecules on trophoblast cells that do not elicit a maternal immune response; (iv) changes in tryptophan catabolisms; (v) T‐cell apoptosis; (vi) complement; and (vii) costimulatory molecules such as the programmed death ligand . Other mechanisms for tolerance are not currently understood.…”
Section: Introductionmentioning
confidence: 99%