Abstract
Blood from healthy non-pregnant, pregnant and postnatal women was used. Circulating lymphocytes were phenotyped using the whole blood FACS lysis method. Multicolour analysis was used to identify CD4+/CD25+ cells with low forward light scatter, thereby differentiating Treg cells from activated lymphocytes. Functional studies confirmed these cells to have suppresser activity. The median proportion of Treg cells was 4.4% (range 2.3–8.0) in the non-pregnant women vs. 9.2% (3.4–28.1) in pregnancy (P < 0.0001). Evidence that these small CD4+/CD25+ T cells were Treg cells rather than recently activated T cells included negative vs. for activation markers DR (88–94%) and CD69 (94–98%), and no increased expression of CD11a or CD18. CD45RO was present on 34–52%, indicating either previous exposure to antigen or that some of these cells may have reverted to CD45RA expression. CXCR3, previously reported on Treg cells and an important chemokine receptor for migration into allografts, was found on 38–50% of Treg cells in pregnancy.