Immunity in the neonatal animal is primarily maternally derived, either by lymphocytes that pass into the newborn across the placenta or following colostrum ingestion. However, the effect of this passively transferred cellular maternal immunity on the newborn's immune repertoire is not clearly understood. Various studies have shown that colostral lymphocytes are activated and possess functional abilities; however, no studies have shown the transfer of colostral antigen-specific T-cell-specific responses in a newborn. In this study we examined the transfer of vaccine-induced Mycoplasma hyopneumoniae cellular immunity from immune dams to newborn piglets. Newborn piglets from vaccinated and nonvaccinated dams were assessed in two ways for cellular immune responses specific to M. hyopneumoniae: (i) delayed-type hypersensitivity (DTH) testing and (ii) in vitro lymphocyte proliferation, assayed on piglet blood lymphocytes and sow colostral lymphocytes. DTH responses to M. hyopneumoniae were detected only for offspring of vaccinated sows, whereas DTH responses to the nonspecific mitogen phytohemagglutinin were seen for all piglets. M. hyopneumoniae-specific proliferation was seen for colostral lymphocytes from vaccinated sows and for blood lymphocytes from neonatal piglets of vaccinated dams but not for blood lymphocytes from piglets of nonvaccinated sows. Functional antigen-specific T cells were transferred to offspring from vaccinated sows and participated in the neonatal immune response upon stimulation. These data have implications for defining disease intervention strategies.The immediate postnatal period is a critical time in the development of young animals' immune systems because it involves a major shift from reliance on innate immunity to adaptive immunity. During this transition period, neonates are protected by passively acquired maternal immunity. In most species, the fetus acquires passive immunity in utero when immune factors cross the placenta. However, some animals, specifically those with epitheliochorial (swine and equine) or hematochorial (bovine) placentation, first receive maternal immunity at birth through colostrum ingestion. Immunomodulatory factors are integral parts of colostrum and include hormones and cytokines, as well as antibodies and a variety of cells (reviewed in reference 22). While an extensive literature exists regarding the immunoglobulin composition of porcine mammary secretions, little attention has been given to colostral cells. There are more than 2 ϫ 10 6 cells per ml in colostrum, approximately 20% of which are lymphocytes, and an estimated 500 million maternal cells transverse the intestinal epithelium daily (3, 10). Interestingly, the transfer of lymphocytes from colostrum into the circulation of the neonate is ordered, not random, indicating an evolutionary importance of maternal lymphocytes (21, 23). The present study investigated whether the colostrum of vaccinated sows (VS) transfers functional antigen-specific lymphocytes to newborn piglets.Contributions by studies of...