4.4 Article

Enhancement of natural and acquired immunity by Lactobacillus rhamnosus (HN001), Lactobacillus acidophilus (HN017) and Bifidobacterium lactis (HN019)

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BRITISH JOURNAL OF NUTRITION
卷 83, 期 2, 页码 167-176

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CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0007114500000210

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probiotics; immunity; lactic acid bacteria

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Consumption of lactic acid bacteria (LAB) has been suggested to confer a range of health benefits including stimulation of the immune system and increased resistance to malignancy and infectious illness. In the present study, the effects of feeding Lactobacillus rhamnosus(HN001, DR20(TM)),Lactobacillus acidophilus(HN017)and Bifidobacterium lactis(HN019, DR10(TM))on in vivo and in vitro indices of natural and acquired immunity in healthy mice were examined. Mice were fed daily with L. rhamnosus, L. acidophilusor B. lactis(10(9) colony forming units) and their immune function was assessed on day 10 or day 28. Supplementation with L. rhamnosus, L. acidophilusor B. lactis resulted in a significant increase in the phagocytic activity of peripheral blood leucocytes and peritoneal macrophages compared with the control mice. The proliferative responses of spleen cells to concanavalin A (a T-cell mitogen) and lipopolysaccharide (a B-cell mitogen) were also significantly enhanced in mice given different LAB. Spleen cells from mice given L. rhamnosus, L. acidophilusor B. lactis also produced significantly higher amounts of interferon-gamma in response to stimulation with concanavalin A than cells from the control mice. LAB feeding had no significant effect on interleukin-4 production by spleen cells or on the percentages of CD4(+), CD8(+) and CD40(+) cells in the blood. The serum antibody responses to orally and systemically administered antigens were also significantly enhanced by supplementation with L. rhamnosus, L. acidophilusor B. lactis. Together, these results suggest that supplementation of the diet with L. rhamnosus(HN001),L. acidophilus(HN017)or B. lactis(HN019)is able to enhance several indices of natural and acquired immunity in healthy mice.

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