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KPV is a naturally occurring tripeptide with anti-inflammatory and immunomodulatory properties, studied for its role in gut inflammation and wound healing.
KPV is a naturally occurring tripeptide with anti-inflammatory and immunomodulatory properties, studied for its role in gut inflammation and wound healing.
KPV (Lysyl-Prolyl-Valine) is a short tripeptide composed of three amino acids: Lysine (K), Proline (P), and Valine (V). It is a naturally occurring C-terminal fragment of the endogenous hormone alpha-melanocyte-stimulating hormone (α-MSH), which plays a key role in regulating immune and inflammatory responses. KPV has attracted significant scientific interest, particularly in the fields of gastroenterology and dermatology.
KPV exerts its effects primarily by inhibiting key pro-inflammatory signaling pathways. The main mechanisms include:
Due to its small size, KPV can cross biological barriers more readily than larger peptides or proteins, enhancing its therapeutic potential.
A major area of research focuses on the use of KPV in inflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis. Preclinical studies demonstrate that KPV – especially in orally available or nanoparticle-encapsulated form – can significantly reduce intestinal inflammation. It is selectively taken up by the intestinal mucosa and acts locally at the site of inflammation.
KPV promotes skin tissue regeneration and has shown accelerating effects on wound healing in experimental models. It can suppress inflammatory skin reactions and is being investigated as a potential therapeutic option for inflammatory skin conditions.
Given its immunomodulatory properties, KPV is also being studied in the context of systemic inflammation and infection, particularly with regard to reducing excessive immune responses.
KPV has been investigated in research using various formulations:
Standardized clinical dosing guidelines for humans do not yet exist, as KPV remains predominantly in the preclinical and early clinical research phase.
KPV is considered well-tolerated due to its endogenous origin. No serious adverse effects have been reported in studies to date. As a very small peptide, systemic immunogenicity is considered unlikely. However, comprehensive clinical trials in humans are needed to fully assess long-term safety and efficacy.
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