US2011182934A1PendingUtilityA1
Immune system stimulating nutrition
Est. expiryJun 13, 2028(~1.9 yrs left)· nominal 20-yr term from priority
A61P 37/00A61P 37/08A61P 37/04A61P 29/00A61P 31/00A61P 1/14A61P 1/12A61P 11/06A61P 17/00A61K 38/018A23V 2002/00A61K 35/744A61K 38/017A23L 33/135A61K 31/702A23L 33/40A61K 35/745A61K 31/733
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Claims
Abstract
Disclosed is a nutritional composition comprising a combination of non-digestible oligosaccharides and a product obtained by incubating an aqueous substrate by bifidobacteria and optionally a product obtained by incubating an aqueous substrate by S. thermophilus. Said combination synergistically improves the immune system by stimulating the Th1 response, and/or decreasing the Th2 response, improving the vaccination response, improving the resistance against infections and/or decreasing allergy.
Claims
exact text as granted — not AI-modified1 - 21 . (canceled)
22 . A process for the manufacture of a preparation, comprising:
(a) incubating bifidobacteria with at least one aqueous substrate selected from the group consisting of milk, milk protein, whey, whey protein, whey protein hydrolysate, casein hydrolysate, and lactose to obtain a first incubated mixture; (b) combining the incubated mixture with at least two different non-digestible carbohydrates, at least one of which is selected from the group consisting of fructo-oligosaccharides, galacto-oligosaccharides, gluco-oligosaccharides, arabino-oligosaccharides, mannan-oligosaccharides, xylo-oligosaccharides, fuco-oligosaccharides, arabinogalacto-oligosaccharides, glucomanno-oligosaccharides, galactomanno-oligosaccharides, raffinose, lactosucrose, sialic acid comprising oligosaccharides and uronic acid oligosaccharides.
23 . The process according to claim 22 , further comprising inactivating and/or removing the bifidobacteria from the first incubated mixture.
24 . The process according to claim 23 , wherein the bifidobacteria are inactivated by heating the first incubated mixture.
25 . The process according to claim 23 , wherein the bifidobacteria are removed from the first incubated mixture by centrifugation, filtration, or both.
26 . The process according to claim 22 , wherein two of the at least two different non-digestible carbohydrates, are selected from the group consisting of fructo-oligosaccharides, galacto-oligosaccharides, gluco-oligosaccharides, arabino-oligosaccharides, mannan-oligosaccharides, xylo-oligosaccharides, fuco-oligosaccharides, arabinogalacto-ologosaccharides, glucomanno-oligosaccharides, galactomanno-oligosaccharides, raffinose, lactosucrose, sialic acid comprising oligosaccharides and uronic acid oligosaccharides.
27 . The process according to claim 22 , wherein the bifidobacteria belong to species B. breve.
28 . The process according to claim 27 , wherein the species B. breve comprises strain B. breve CNCM I-2219.
29 . The process according claim 22 , further comprising:
(i) incubating Streptococcus thermophilus, with a substrate selected from the group consisting of milk, milk protein, whey, whey protein, whey protein hydrolysate, casein, casein hydrolysate, and lactose, to obtain a second incubated mixture; (ii) optionally inactivating the S. thermophilus by heating the second incubated mixture of (i) and/or removing S. thermophilus by centrifugation, filtration or both; and (iii) combining the first and second incubated mixtures.
30 . The process according to claim 29 , wherein the Streptococcus thermophilus comprises strain S. thermophilus CNCM I-1620.
31 . The process according to claim 22 , wherein one or both of the at least two different non-digestible carbohydrates are selected from the group consisting of galacto-oligosaccharides and fructo-oligosaccharides.
32 . The process according to claim 22 , further comprising inoculating the substrate with bifidobacteria in amount of between 1×10 2 to 1×10 11 cfu per ml substrate at a temperature of between 20° C. to 50° C., for at least 2 h and at a pH of between 4 and 8.
33 . The process according to claim 29 , further comprising inoculating the substrate of (i) with Streptococci in amount of between 1×10 2 to 1×10 11 cfu per ml substrate at a temperature of between 20° C. to 50° C., for at least 2 h and at a pH of between 4 and 8.
34 . The process according to claim 29 , wherein the first or the second incubated mixtures are inactivated by heating for at least 5 minutes at a temperature above 50° C.
35 . The process according to claim 22 , further comprising a drying step.
36 . The process according to claim 22 , wherein only one non-digestible carbohydrate is added, said non digestible carbohydrate being fructo-oligosaccharide.
37 . A nutritional composition obtained by the process of claim 22 .
38 . The nutritional composition according to claim 37 , having a viscosity of 1 to 60 mPa·s at a shear rate of 100 s −1 at 20° C.
39 . A nutritional composition comprising, based on total dry weight of the composition:
(a) 0.5 to 10 wt. % of the sum of galacto-oligosaccharides and fructo-oligosaccharides, and (b) 5 to 99.5 wt. % of the preparation obtained by the process of claim 22 , wherein the bifidobacteria in step a belong to the species B. breve.
40 . The nutritional composition of claim 39 , further comprising (c) 2 to 94.5 wt. % the preparation obtained by:
(i) incubating Streptococcus thermophilus, with a substrate selected from the group consisting of milk, milk protein, whey, whey protein, whey protein hydrolysate, casein, casein hydrolysate, and lactose, to obtain a second incubated mixture; (ii) optionally inactivating the S. thermophilus by heating the second incubated mixture of (i) and/or removing S. thermophilus by centrifugation, filtration or both; and (iii) combining the first and second incubated mixtures.
41 . The nutritional composition according to claim 39 , comprising less than 10 3 du living bifidobacteria per g dry weight of the preparation.
42 . A method of treating a disease and/or infection and/or enhancing response to vaccination, comprising administering to a subject in need thereof a composition according to claim 39 .
43 . The method according to claim 38 , wherein the disease is an immune disorder selected from the group consisting of asthma, allergy, atopic dermatitis, allergic conjunctivitis, dust mite allergy, urticaria and allergic rhinitis.
44 . The method according to claim 42 , wherein the subject suffers from at least one of the following: (a) immunosenescence, (b) HIV and/or AIDS, (c) cancer, (d) chronic obstructive pulmonary disease and (e) diabetes.Join the waitlist — get patent alerts
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