Methods, compositions, and devices for supplying dietary fatty acid needs
US-12059391-B2 · Aug 13, 2024 · US
US9439448B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9439448-B2 |
| Application number | US-201213615701-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 14, 2012 |
| Priority date | Jun 30, 2005 |
| Publication date | Sep 13, 2016 |
| Grant date | Sep 13, 2016 |
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A nutritional composition for improving the immunological function of a subject, including a lipid or fat; a protein source; about 5 to about 100 mg/100 kcal of a source of long chain polyunsaturated fatty acids which comprises docosahexanoic acid; and about 0.1 to about 1 mg/100 kcal of a prebiotic composition, wherein the prebiotic composition comprises at least 20% of an oligosaccharide which has a fermentation rate which is demonstrably slower than that of galacto-oligosaccharide.
Opening claim text (preview).
What is claimed is: 1. A method for promoting oral tolerance to food protein antigens in an infant, comprising administering to the infant a nutritional composition comprising a. a lipid or fat; b. a protein source; c. about 5 to about 100 mg/100 kcal of a source of long chain polyunsaturated fatty acids which comprises docosahexanoic acid; d. about 1.0 to about 10.0 g/L of a prebiotic composition, wherein the prebiotic composition comprises at least 20% of an oligosaccharide which has a fermentation rate which is demonstrably slower than that of galacto-oligosaccharide; and e. about 2500 pg to about 10,000 pg TGF-B per mL of composition, wherein the ratio of TGF-β1: TGF-β2 is about 1:1 to about 1:20, and wherein the combination of TGF-β and the prebiotic contributes to the induction of oral tolerance to antigens in an infant, wherein the infant had established oral tolerance to the antigens but oral tolerance has since failed. 2. The method of claim 1 , wherein the prebiotic composition comprises polydextrose. 3. The method of claim 1 , wherein the prebiotic composition further comprises galacto-oligosaccharide. 4. The method of claim 1 , wherein the composition further comprises at least one probiotic. 5. The method of claim 4 , wherein the probiotic is selected from the group consisting of Lactobacillus rhamnosus GG, Bifidobacterium longum , and Bifidobacterium animalis subsp. Lactis BB-12. 6. The method of claim 4 , wherein the probiotic comprises a non-viable probiotic. 7. The method of claim 1 , wherein the nutritional composition further comprises a bioactive-enhanced whey fraction. 8. The method of claim 1 , wherein the nutritional composition further comprises at least one nucleotide selected from the group consisting of cytidine 5′-monophosphate, uridine 5′-monophosphate, adenosine 5′-monophosphate, and guanosine 5′-monophosphate. 9. The method of claim 1 , wherein the protein source comprises glutamine-containing peptides. 10. The method of claim 1 , wherein the protein source comprises from about40% to about 80% whey protein. 11. The method of claim 1 , wherein the protein source comprises from about20% to about 60% casein protein. 12. The method of claim 1 , wherein the protein source comprises intact protein and partially hydrolyzed protein. 13. The method of claim 1 , wherein the protein source comprises hydrolyzed protein having a degree of hydrolysis of between about 4% and 10%.
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