Abstract
The most abundant lymphocyte present in decidual tissue is the CD8(+) T cell. It has been shown that most decidual CD8(+) T cells have an effector -memory phenotype, but expressed reduced levels of perforin and granzyme B compared with the peripheral CD8(+) effector -memory T cells. The specificity of these CD8(+) memory T cells has yet to be determined. One hypothesis is that the decidual memory T cells are virus-specific T cells that should protect the fetus against incoming pathogens. As virus-specific CD8+ memory T cells can cross-react with human leukocyte alloantigens, an alternative, but not mutually exclusive, hypothesis is that these CD8(+) T cells are fetus-specific. Using virus-specific tetramers, we found increased percentages of virus-specific CD8(+) T cells in decidual tissue compared with peripheral blood after uncomplicated pregnancy. So far, no evidence has been obtained for a cross-reactive response of these virus-specific T cells to fetal human leukocyte antigens. These results suggest that the virus-specific memory T cells accumulate in the placenta to protect the fetus from a harmful infection. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 1-8 |
| Number of pages | 8 |
| Journal | Journal of Reproductive Immunology |
| Volume | 113 |
| DOIs | |
| Publication status | Published - Feb-2016 |
Keywords
- Human
- Decidua
- Normal pregnancy
- CD8(+) memory T cells
- Virus-specific
- PATERNAL HLA ANTIGENS
- HUMAN-PREGNANCY
- TROPHOBLAST CELLS
- PERIPHERAL-BLOOD
- IMMUNE-RESPONSE
- CTL RESPONSE
- PREECLAMPSIA
- LYMPHOCYTES
- INFECTION
- FETUS