LAUSR

&NA; Clinacanthus nutans (Burm. f.) Lindau is a traditional medicinal plant belonging to the Acanthaceae family. Its therapeutic potentials have been increasingly documented particularly the antiviral activity against Herpes Simplex Virus (HSV), anti‐cancer, anti‐oxidant, anti‐inflammatory and immunomodulatory activities. However, majority of these studies used crude or fractionated extracts and not much is known about individual compounds from these extracts and their biological activities. In the present study, we have isolated four compounds (CN1, CN2, CN3 and CN4) from the hexane fractions of C. nutans leaves. Using NMR spectroscopic analysis, these compounds were identified to be shaftoside (CN1), stigmasterol (CN2), &bgr;‐sitosterol (CN3) and a triterpenoid lupeol (CN4). To determine the immunosuppressive potential of these compounds, their effects on mitogens induced T and B lymphocyte proliferation and the secretion of helper T cell cytokines were examined. Among the four compounds, stigmasterol (CN2) and &bgr;‐sitosterol (CN3) were shown to readily inhibit T cell proliferation mediated by Concanavalin A (ConA). However, only &bgr;‐sitosterol (CN3) and not stigmasterol (CN2) blocks the secretion of T helper 2 (Th2) cytokines (IL‐4 and IL‐10). Both compounds have no effect on the secretion of Th1 cytokines (IL‐2 and IFN‐&ggr;), suggesting that &bgr;‐sitosterol treatment selectively suppresses Th2 activity and promotes a Th1 bias. CN3 was also found to significantly reduce the proliferation of both T helper cells (CD4+CD25+) and cytotoxic T cells (CD8+CD25+) following T cell activation induced by ConA. These results suggested that phytosterols isolated from C. nutans possess immunomodulatory effects with potential development as immunotherapeutics. HighlightsStigmasterol, &bgr;‐sitosterol, lupeol, and shaftoside are the bioactive compounds in C. nutans.&bgr;‐Sitosterol and stigmasterol inhibit T cell proliferation mediated by ConA.&bgr;‐Sitosterol suppresses Th2 (IL‐4 and IL‐10) but not Th1 cytokines secretion.&bgr;‐Sitosterol reduces activated T helper (CD4+CD25+) and cytotoxic T cells (CD8+CD25+) proliferation.Both &bgr;‐sitosterol and stigmasterol can potentially be developed into immunotherapeutic agents.