A novel extract from bovine colostrum whey supports anti-bacterial and anti-viral innate immune functions in vitro and in vivo I. Enhanced immune activity in vitro translates to improved microbial clearance in animal infection models
被引:26
作者:
Benson, Kathleen F.
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NIS Labs, Klamath Falls, OR 97601 USANIS Labs, Klamath Falls, OR 97601 USA
Benson, Kathleen F.
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Carter, Steve G.
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NIS Labs, Klamath Falls, OR 97601 USANIS Labs, Klamath Falls, OR 97601 USA
Carter, Steve G.
[1
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Patterson, Kelly M.
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NIS Labs, Klamath Falls, OR 97601 USANIS Labs, Klamath Falls, OR 97601 USA
Patterson, Kelly M.
[1
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Patel, Dilip
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S Dakota State Univ, Brookings, SD 57007 USA
Sterling Technol Inc, Brookings, SD 57006 USANIS Labs, Klamath Falls, OR 97601 USA
Patel, Dilip
[2
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Jensen, Gitte S.
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NIS Labs, Klamath Falls, OR 97601 USANIS Labs, Klamath Falls, OR 97601 USA
Objective. To evaluate effects on the innate immune system after exposure to, a consumable low-molecular weight fraction (CLMWF) of immunoglobulin-depleted bovine colostrum whey. Methodology. Cell-based immune assays were performed in vitro, and host resistance towards bacterial and viral infection was evaluated in two mouse studies. Results. In vitro data showed a multimodal effect, as CLMWF treatment resulted in a rapid increase in phagocytosis. CLMWF increased chemotaxis of polymorphonuclear cells towards the bacterial peptide f-MLP. CLMWF treatment of natural killer cells increased expression of the CD69 activation marker. Mononuclear phagocytes showed decreased numbers of CD14(bright) and increased number of CD14(dim) cells. The remaining CD14(bright) cells showed reduced expression of CD80 and CD86, whereas CD14(dim) cells showed increased expression of CD80 and CD86, suggesting dendritic cell maturation. Mouse models were applied to evaluate the immune-modulating capacity of CLMWF when consumed acutely during bacterial (Streptococcus) and viral (Influenza) infections in vivo. Reduced bacterial and viral loads were observed in lungs within 24 h. Viral load was also reduced when CLMWF was introduced intranasally. Conclusion. The data suggest that the support of antimicrobial immune defense mechanisms and maturation of antigen-presenting cells in vitro translates to protection in vivo when product is introduced across mucosal membranes. (C) 2012 Elsevier Inc. All rights reserved.