Coccomyxa sp.KJ extract affects the fate of T cells stimulated by toxic shock syndrome toxin-1, a superantigen secreted by Staphylococcus aureus.
Shino OhshimaSatoko KomatsuHirofumi KashiwagiYumiko GotoYusuke OhnoSoga YamadaAkiko KannoTomoka ShimizuToshiro SekiAtsushi YasudaHitoshi KunoYoshie KametaniPublished in: Microbiology and immunology (2022)
T cell stimulation by bacterial superantigens induces a cytokine storm. After T cell activation and inflammatory cytokine secretion, regulatory T cells (Treg) are produced to suppress the immune response. Coccomyxa sp.KJ (IPOD FERM BP-22254), a green alga, is reported to regulate immune reactions. Therefore, we examined the effects of Coccomyxa sp.KJ extract (CE) on the superantigen-induced immune response. When human peripheral blood mononuclear cells (PBMCs) were stimulated with toxic shock syndrome-1 (TSST-1) in the presence of CE, the number of activated T cells decreased moderately. Purified T cells stimulated in the presence of CE comprised more non-proliferating cells than those stimulated in the absence of CE, whereas some T cells proliferated more quickly. The levels of activation markers on the stimulated T cells increased in the presence of CE. Most of the inflammatory cytokines did not change but IL-1β, IL-17, IL-4, and IL-13 secretion increased, whereas that of IL-2, TNF-α, and IL-18 decreased. IL-10 secretion was also decreased by CE treatment, suggesting that the immune response was not suppressed by Treg cells. CE enhanced the expression of stem cell-like memory cell markers in T cells. These results suggest that CE can regulate the fate of T cells and can help to ameliorate superantigen-induced T cell hyperactivation and immune suppression.
Keyphrases
- immune response
- regulatory t cells
- stem cells
- staphylococcus aureus
- energy transfer
- oxidative stress
- escherichia coli
- dendritic cells
- rheumatoid arthritis
- diabetic rats
- toll like receptor
- pseudomonas aeruginosa
- working memory
- mesenchymal stem cells
- combination therapy
- anti inflammatory
- methicillin resistant staphylococcus aureus
- induced pluripotent stem cells
- pluripotent stem cells