Pregnancy promotes tolerance to future offspring by programming selective dysfunction in long-lived maternal T cells. Issue 4 (3rd November 2016)

• Record Type: Journal Article
• Authors: Barton, Brendan M; Xu, Rong; Wherry, E John; Porrett, Paige M
• Is Part Of: Journal of leukocyte biology. Volume 101:Issue 4(2017)
• Page Start: 975
• Page End: 987
• Publication Date: 2016-11-03
• Subjects: alloimmunization -- transplantation -- exhaustion -- PD-1 -- fetomaternal; Leucocytes -- Periodicals; Reticulo-endothelial system -- Periodicals; 571.96
• DOI: 10.1189/jlb.1A0316-135R
• Languages: English
• ISSNs: 0741-5400

Abstract

Abstract : Dysfunctional memory CD8 + T cells differentiate in the maternal repertoire which promotes pregnancy success, but can threaten subsequent tissue grafts. Abstract: Fetal antigen available during pregnancy induces the proliferation of maternal T cells. It is unknown, however, whether these antigen-activated T cells differentiate into long-lived memory T cells that are capable of mediating rapid-recall responses to tissue antigens. To test the hypothesis that pregnancy induces an alternative fate in fetal-specific maternal T cells, we used a murine model to track longitudinally fetal-specific T cells in pregnant and postpartum animals and test the response of these cells when challenged with the same antigen during sequential pregnancy or skin transplantation. Fetal-specific CD8 + T cells were robustly primed during pregnancy but failed to acquire robust effector functions. These primed cells persisted long term in postpartum animals, frequently maintained a programmed death 1 (PD-1) + phenotype, and failed to expand or produce cytokines robustly in response to second pregnancy or skin transplantation. However, whereas there was no impact on second pregnancy as a result of the persistence of fetal-primed memory CD8 + T cells in the mother, skin grafts bearing the same antigen were rejected more rapidly. Altogether, our data suggest that fetal antigen exposure during pregnancy induces the differentiation of long-lived maternal CD8 + T cells with context-dependent, selective effector dysfunction. This programmed effector dysfunction provides temporal and systemic restraint of maternal anti-fetal alloreactivity to promote reproductive fitness efficiently, while preserving potentially protective effector T cell responses.