Maternal anti-placental reactivity in natural, immunologically-mediated fetal resorptions.

• DOI: 10.4049/jimmunol.152.10.4903
• Publication Date: 2022-12-31T10:28:37Z
• Authors: S Tangri; T G Wegmann; H Lin; R Raghupathy
• Keywords: Male; 0301 basic medicine; Mice, Inbred BALB C; 0303 health sciences; Placenta; Fetal Resorption; Lymphocyte Activation; Immunotherapy, Adoptive; 3. Good health; Mice; 03 medical and health sciences; Mice, Inbred DBA; Pregnancy; Histocompatibility Antigens; Mice, Inbred CBA; Animals; Cytokines; Pregnancy, Animal; Female; Lymphocyte Culture Test, Mixed

Abstract Observations on maternal recognition of the fetus and the demonstration of the effects of cytokines on reproductive events led to the "immunotrophism" model, which suggests that maternal immune recognition of fetally-derived Ags results in the release of cytokines that promote the growth of the placenta; any disturbance in this balance of cytokines could result in deleterious consequences for the placenta and, in turn, the fetus. We have focused our attention on the murine CBA/J x DBA/2 model of spontaneous abortions and compared them with normal CBA x BALB/c pregnancies. Our results indicate that the extent of stimulation of maternal strain lymphocytes in response to stimulator placental cells in mixed lymphocyte-placenta reactions (MLPR) was much higher in the normal mating combination compared with the abortion-prone mating combination. Cytokine analysis of the supernatants from MLPR indicates that there is significantly higher production of TNF-alpha, IFN-gamma, and IL-2 in supernatants from the abortion-prone combination than in supernatants from the normal combination. Furthermore, MLPR-stimulated cells induce resorptions in normal pregnant mice; maternal strain lymphocytes stimulated by placentas from the abortion-prone combination induce high rates of fetal resorptions, but lymphocytes stimulated with placentas from the normal combination do not. Together, these results suggest that immunologically mediated fetal resorptions probably result from improper or inappropriate maternal responses to placental Ags. Our observations also suggest that such effects are probably mediated by cytokines.