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Human Placental and Decidual Organ Cultures to Study Infections at the Maternal-fetal Interface
Published on: July 21, 2016
Immunosuppressive activity in buffalo placenta
1Animal Biochemistry Division, National Dairy Research Institute, Karnal, India.
Insights
Buffalo placenta proteins suppress lymphocyte proliferation in a dose-dependent manner. These immunosuppressive proteins, found in various placental fractions, were not reversed by interleukin-1, indicating potential immunomodulatory roles.
Area of Science:
- Immunology
- Veterinary Science
- Biochemistry
Background:
- The placenta plays a crucial role in maternal-fetal tolerance.
- Investigating placental components can reveal immunomodulatory factors.
Purpose of the Study:
- To evaluate the immunosuppressive activity of buffalo placenta proteins.
- To characterize the nature of these immunosuppressive factors.
Main Methods:
- Lymphocyte proliferation assays were performed using phytohaemagglutinin (PHA) with varying concentrations of placental proteins.
- Proteins were fractionated using ammonium sulphate precipitation and size exclusion chromatography (G-100 column).
- The effect of interleukin-1 (IL-1) on immunosuppression was assessed.
Main Results:
- Buffalo placental proteins demonstrated dose-dependent immunosuppressive activity.
- Proteins from both cotyledon and non-cotyledon portions exhibited immunosuppression.
- Ammonium sulphate fractions and G-100 column peaks showed significant lymphocyte proliferation suppression (55-75%).
- Interleukin-1 did not reverse the observed immunosuppression.
Conclusions:
- Buffalo placenta contains potent immunosuppressive proteins.
- These proteins affect lymphocyte proliferation independently of IL-1 signaling.
- Further research into these placental factors may offer insights into immunomodulation.
Abstract:
Immunosuppressive activity in buffalo placenta was evaluated by measuring proliferation of lymphocytes in presence of phytohaemagglutinin (PHA) alone or PHA plus placental proteins. The immunosuppressive activity was dose-dependent over the protein concentration range of 10-50 micrograms/ml. Proteins from both cotyledon and non-cotyledon portions of placenta exhibited immunosuppressive activity. Fractions obtained with 0-40, 40-60 and 60-80% saturated ammonium sulphate exhibited 70, 73 and 75% suppression, respectively. PBS-soluble placental proteins were resolved on G-100 column into three peaks that exhibited 69 (peak 1), 55 (peak 2) and 73% (peak 3) suppression. Exogenously added interleukin-1 (IL-1) failed to reverse the suppression caused by buffalo placental proteins.
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