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Application of Long-term cultured Interferon-γ Enzyme-linked Immunospot Assay for Assessing Effector and Memory T Cell Responses in Cattle
Published on: July 11, 2015
[Immunomodulatory and anti-oxidant effects of bovine lactoferrin in man]
N Paul-Eugène1, B Dugas, J P Kolb
1Besnier/Bridel Recherche et Développement, Retiers, France.
Insights
Lactoferrin (Lf) modulates human monocyte activation, inhibiting free radical generation and enhancing cytokine production. Copper-substituted Lf shows the strongest antioxidant effect, while Lf
Area of Science:
- Immunology
- Biochemistry
- Cell Biology
Context:
- Human monocyte activation is a key process in immune responses.
- Lactoferrin (Lf) is an iron-binding glycoprotein with diverse biological activities.
- The role of metal substitution in Lf's immunomodulatory functions requires further elucidation.
Purpose:
- To investigate the differential effects of lactoferrin (Lf) and its metal-substituted forms on normal human monocyte activation.
- To determine the impact of cation substitution on Lf's antioxidant and immune-stimulating properties.
- To assess Lf's influence on cytokine and prostacyclin production, as well as monocyte phenotype modulation.
Summary:
- Lactoferrin (Lf) differentially affects human monocyte activation, inhibiting PMA-induced free radical generation.
- The antioxidant capacity of Lf is modulated by the substituting divalent cation, with copper (Cu2+) being the most potent.
- Lf, independent of its cation, potentiates lipopolysaccharide (LPS)-induced production of cytokines (IL-1β, TNF-α, IL-6) and prostacyclin (PGI2).
- Lf enhances IL-4-induced release of soluble CD23 (sCD23) without altering monocyte phenotype.
Impact:
- These findings highlight the complex immunomodulatory roles of lactoferrin.
- The study provides insights into how metal substitution influences Lf's biological activity.
- Understanding these mechanisms could inform therapeutic strategies involving lactoferrin in inflammatory and immune conditions.
Abstract:
Lf presented differential effects in the induction of normal human monocyte activation. Lf inhibits the free radical generation by normal human monocytes in response to PMA. This effect on free radical generation is linked to the nature of the divalent cationic metal that substitutes the Apo-Lf. Indeed, the substitution of Fe2+ by another cationic transition metal (Cu2+, Zn2+, Pt2+ or Au2+) modifies the anti-oxidant effect of Lf. Among the different substituted Lf the Lf saturated with Cu2+ is the more potent inhibitor of free radical generation by normal human monocytes. In addition to its anti-oxidant effect, Lf stimulates, in combination with LPS, the production of cytokines (IL-1 beta, TNF-alpha and IL-6) and of prostacyclin (PGI2) by normal human monocytes. This potentiating effect is independent of the cation that substitutes the Lf, since the Apo-Lf is able to induce such a potentiating effect. In addition, whereas Lf does not modulate the phenotype of normal human monocytes stimulated or not with IL-4 it does enhance the IL-4-induced release of the soluble form of CD23 by these cells.
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