SUMMARYThe mammary gland (MG) develops new vasculature and is colonized by lymphocytes, primarily T-cells, during pregnancy. In contrast, during lactation it is colonized primarily by IgA-containing B-cells (c-IgA cells). To explain this difference, we analyzed the spatiotemporal relationships between lymphocytes that expressed peripheral or mucosal homing receptors (HR) and the location of their vascular counterreceptors using quantitative immunohistochemical techniques. We observed that the density of  7 ϩ /CD3 ϩ T-cells varied with the amount of the mucosal addressin cell adhesion molecule-1 (MAdCAM-1)-stained area. Both increased during pregnancy to peak at delivery, decreased rapidly in early lactation to a steady level in mid-and late lactation, and returned to resting values after weaning. Although 60% of these  7 ϩ /CD3 ϩ T-cells scattered in the epithelium co-expressed ␣ E  7 , whereas the remaining 40% in association with blood vessels were ␣ 4  7 , these results are consistent with a role of MAdCAM-1 in the localization of ␣ 4  7 ϩ T-cells. In contrast to T-cells,