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. [1 ]
Carter, Steve G. [1 ]
Patterson, Kelly M. [1 ]
Patel, Dilip [2 ,3 ]
Jensen, Gitte S. [1 ]
机构
[1] NIS Labs, Klamath Falls, OR 97601 USA
[2] S Dakota State Univ, Brookings, SD 57007 USA
[3] Sterling Technol Inc, Brookings, SD 57006 USA
关键词
Proline-rich polypeptide; Bacterial; Viral; Infection; Innate; Immunity; Macrophage; Dendritic; Maturation; Phagocytosis; POLYPEPTIDE COMPLEX PRP; GROWTH-FACTORS; CELLS; MILK; LACTOFERRIN; MODULATION; MICE; SUPPLEMENTATION; LACTOPEROXIDASE; COMPONENTS;
D O I
10.1016/j.ypmed.2011.12.023
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
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.
引用
收藏
页码:S116 / S123
页数:8
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