US2017281757A1PendingUtilityA1
PROBIOTICS, SECRETORY IgA AND INFECTION
Est. expiryJun 24, 2028(~1.9 yrs left)· nominal 20-yr term from priority
A61P 37/04A61P 37/02A61P 31/04A61P 31/00A61P 29/00A61P 33/02A61P 1/00A61K 35/747A61K 35/745A23V 2002/00A61K 39/395A61K 35/744A23L 33/135A61K 35/741A23L 33/40A61K 2300/00Y02A50/30
51
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Claims
Abstract
Ways to increase the effectiveness of probiotics are disclosed. One embodiment relates to a combination of probiotics with secretory IgA and possible uses of this combination. For example, a method of using a composition containing secretory IgA and at least one probiotic to prepare a product to treat or prevent infection is disclosed.
Claims
exact text as granted — not AI-modifiedThe invention is claimed as follows:
1 . A method for treating, preventing or reducing non-viral infections, the method comprising the step of:
administering a therapeutically-effective amount of a composition comprising SIgA and probiotic microorganisms, wherein the SIgA and the probiotic microorganisms are present in the form of a complex with each other, and the SIgA and the probiotic micro-organisms are present in the composition in a stoichiometric ratio of at least 100:1.
2 . The method according to claim 1 wherein the composition is administered to newborns, infants, juveniles, adults, elderly, or mothers during pregnancy or lactation.
3 . The method according to claim 1 , wherein the composition comprises milk obtained from an animal or plant source.
4 . The method according to claim 1 , wherein the composition comprises at least one of cows' milk, human milk, sheep milk, goat milk, horse milk, camel milk, rice milk or soy milk.
5 . The method according to claim 1 , wherein the composition comprises milk protein fractions or colostrum.
6 . The method according to claim 1 , wherein the composition contains at least one prebiotic.
7 . The method according to claim 6 , wherein the at least one prebiotic is selected from the group consisting of: oligosaccharides; dietary fibers; inulin; or mixtures thereof.
8 . The method according to claim 7 , wherein the oligosaccharides contain at least one of fructose, galactose or mannose.
9 . The method according to claim 7 , wherein the dietary fibers comprise at least one of soluble fibers or soy fibers.
10 . The method according to claim 6 , wherein the at least one prebiotic is selected from the group consisting of: fructo-oligosaccharides (FOS), galacto-oligosaccharides (GOS), isomalto-oligosaccharides, xylo-oligosaccharides, oligosaccharides of soy, glycosyl sucrose (GS), lactosucrose (LS), lactulose (LA), palatinose-oligosaccharides (PAO), maltooligosaccharides, pectins and/or hydrolysates thereof.
11 . The method according to claim 1 , wherein the composition comprises between 10 2 and 10 10 cells of probiotic micro-organism per daily dose.
12 . The method according to claim 1 , wherein the composition comprises between 0.0001 mg SlgA and 10 mg SlgA per daily dose.
13 . The method according to claim 1 , wherein the probiotic microorganisms are selected from the group consisting of Bifidobacterium, Lactobacillus, Streptococcus, Saccharomyces and mixtures thereof.
14 . The method according to claim 1 , wherein the probiotic microorganisms are selected from the group consisting of Bifidobacterium longum, Bifidobacterium lactis, Lactobacillus acidophilus, Lactobacillus rhamnosus, Lactobacillus paracasei, Lactobacillus johnsonii, Lactobacillus plantarum, Lactobacillus salivarius, Enterococcus faecium, Saccharomyces boulardii and Lactobacillus reuteri, and mixtures thereof.
15 . The method according to claim 11 , wherein the probiotic microorganisms are selected from the group consisting of: Lactobacillus johnsonii (NCC533; CNCM I-1225), Bifidobacterium longum (NCC490; CNCM 1-2170), Bifidobacterium longum (NCC2705; CNCM 1-2618), Bifidobacterium lactis (2818; CNCM 1-3446), Lactobacillus paracasei (NCC2461; CNCM 1-2116), Lactobacillus rhamnosus GG (ATCC53103), Lactobacillus rhamnosus (NCC4007; CGMCC 1.3724), Enterococcus faecium SF 68 (NCIMB10415), and mixtures thereof.
16 . The method according to claim 1 , wherein the SIgA is isolated SIgA.
17 . The method according to claim 1 , wherein at least 90% of the probiotic microorganisms present in the composition are associated with at least one SIgA molecule as immune complexes.Join the waitlist — get patent alerts
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