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Updated: Apr 27, 2026

Isolation and Activation of Murine Lymphocytes
Published on: October 30, 2016
Augmentation of lymphocytes activation and T cell modulation by the extracts from some Euphorbia species
Mehri Ghafourian Boroujerdnia1, Neda Khosravi, Saeed Malek-Hosseini
1Department of Immunology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences , Ahvaz , Iran .
Context:
Euphorbia is an important Euphorbiaceae genus that is traditionally being used for various infections, inflammation, and cancer.
Objective:
The present study investigated the possible in vitro immunomodulatory effect of three species of Euphorbia genus including Euphorbia microciadia Boiss, Euphorbia osyridea Boiss, and Euphorbia heteradenia Jaub. & Sp. on lymphocyte activation and cytokine secretion.
Materials And Methods:
Human lymphocytes were cultured in the presence of various concentrations (0.1-200 µg/ml) of the butanol/hexane extracts of the plants in the presence or absence of phytohemmagglutinin (PHA). The activation of lymphocytes after 48 h was determined by a proliferation assay. The release of T cell cytokines was studied to determine the dominant T cell subsets involved in the immune response.
Results:
All three plant extracts increased the proliferation of PHA-treated lymphocytes (maximum; 132% of control). Extract treatment of lymphocytes in the absence of PHA resulted in an increased proliferation of the cells indicating their lymphocyte mitogenic activity (maximum at 10 µg/ml E. microciadia extract; 494.5 ± 42.2% of control, p < 0.01). The extracts of E. microciadia and E. osyridea could increase IL-4 and IL-10 secretion but not IFN-γ production showing their capacity to deviate immune response toward a Th2 pattern. Euphorbia heteradenia did not change the release of IL-4 and IFN-γ cytokines but increased IL-10 production. The three extracts stimulated lymphocytes to produce IL-17 which showed their possible effects on Th17 cells activation.
Conclusion:
The studied extracts had the ability to modulate T cell responses suggesting their possible beneficial effects on immune host defense.
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