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"Immunomodulation by immune cells in stromal vascular fraction" does **not refer to a specific molecule or receptor**, but rather describes the collective ability of various immune and stromal cells present in the adipose-derived stromal vascular fraction (SVF) to modulate immune responses. The SVF is a heterogeneous mixture obtained from adipose tissue that includes adipose-derived stem cells, T cells, macrophages, endothelial progenitor cells, pericytes, and other cell types[3][4]. These cellular components can exert potent anti-inflammatory and immunoregulatory effects through secretion of cytokines such as interleukin 10 and by promoting regulatory T cell induction and alternative activation of macrophages (\"M2-type\"), which are associated with tissue repair and attenuation of inflammation[1][5]. This immunomodulatory capacity has been investigated for therapeutic potential in autoimmune diseases like multiple sclerosis as well as broader regenerative medicine applications. However, because this entry refers to an overall biological process mediated by many different cell types rather than an individual molecular entity or canonical drug target such as a receptor or enzyme, it is **not considered a therapeutic target** under standard definitions used for drug discovery purposes[1][3]. In summary: \"Immunomodulation by immune cells in SVF\" is not itself a canonical molecular target but describes the functional property of mixed-cell populations within stromal vascular fraction preparations.
null (not a single target; refers to collective actions of various immune cells within SVF)
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