US2012263695A1PendingUtilityA1
Composition having strains of lactobacillus fermentum
Est. expiryAug 11, 2029(~3 yrs left)· nominal 20-yr term from priority
A61P 9/10A61P 3/06A61P 5/16A61P 37/00A61P 9/12A61P 3/10A61P 5/48A61P 37/08A61P 31/00A61P 25/00A61P 31/10A61P 29/00A61P 27/02A61P 3/00A61P 31/18A61P 31/06A61P 1/04A61P 19/02A61P 11/06A61P 19/04A61P 1/12A61P 1/00A61P 17/00A61P 11/00A61P 21/04A61P 17/06A61K 35/747C12Q 1/689A23V 2002/00A23L 33/135A23V 2400/143A23V 2400/169
27
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Claims
Abstract
The invention relates to a pharmaceutical and/or dietetic composition for increasing the impact of the immune defense of higher living beings, wherein bacteria of the species Lactobacillus fermentum from at least one of the strains K1-Lb1 or K1-Lb6 or K2-Lb4 or K6-Lb4 or K7-Lb1 or K8-Lb1 or K9-Lb6 are contained in order to control the adaptive and natural immune defense by means of T helper 1 and T helper 2 cells and/or bacteria of the species Lactobacillus fermentum from at least one of the strains K2-Lb6 or K11-Lb3 are contained in order to strengthen the native immune defense.
Claims
exact text as granted — not AI-modified1 . Pharmaceutical and/or dietetic composition for strengthening the effect of the human immune defense, characterized in that, to strengthen the adaptive immune defence by means of T helper 1 and T helper 2 cells, bacteria
of the genus Lactobacillus fermentum of at least one of the strains K1-Lb1 or K1-Lb6 or K2-Lb4 or K6-Lb4 or K7-Lb1 or K8-Lb1 or K9-Lb3 and/or of the genus Lactobacillus plantarum of the strain K4-Lb6 and/or, to strengthen the native immune defence, bacteria of the genus Lactobacillus fermentum of at least one of the strains K2-Lb6 or K11-Lb3
are contained.
2 . Composition according to claim 1 , characterized in that each strain is contained in Kimere.
3 . Composition according to one of the preceding claims, characterized in that the strengthening of the adaptive immune defense is a shift from the T helper 2 to the T helper 1 reactions.
4 . Composition according to claim 3 , characterized in that at least one of the strains
K1-Lb1 or K1-Lb6 or K2-Lb4 or K4-Lb6 or K6-Lb4 or K9-Lb3
is contained.
5 . Composition according to one of the preceding claims, characterized in that the strengthening of the adaptive immune defense is a shift from the T helper 1 to the T helper 2 responses.
6 . Composition according to one of the preceding claims, characterized in that the strengthening of the adaptive immune defense is an inhibition of inflammations.
7 . Composition according to claim 5 or 6 , characterized in that at least one of the strains
K6-Lb4 or
K7-Lb1 or
K8-Lb1
is contained.
8 . Composition according to one of the preceding claims, characterized in that the strengthening of the adaptive immune defense is an increased release of defensin (hBD) from intestinal cells.
9 . Composition according to claim 8 , characterized in that at least one of the strains
K2-Lb6 or K11-Lb3
is contained.
10 . Composition according to one of the preceding claims, characterized in that the strains tolerate a 0.3% bile salt solution.
11 . Composition according to one of the preceding claims, characterized in that the strain K4-Lb6 tolerates a 3.0% bile salt solution.
12 . Composition according to one of the preceding claims, characterized in that at least 8% of the strains survive a pH of 3.0 for at least 3 h.
13 . Composition according to claim 12 , characterized in that at least one of the strains K1-Lb1 or K1-Lb6 or
K2-Lb4 or K2-Lb6 or K4-Lb6 or K6-Lb4 or K7-Lb1 or K8-Lb1 or K9-Lb3
is contained.
14 . Composition according to one of the preceding claims, characterized in that, to influence the concentration and composition of glycosidic compounds at the membrane or at the wall of a bacterium, and therefore to modulate the immune response of a host, at least one of the strains expresses
a glycosyl transferase or a sugar transferase or an acyl transferase or a lipoteichonic acid-exporting protein.
15 . Composition according to claim 14 , charazterized in that, for at least one of the strains for glycosyl transferase, the sugar residue docking can be catalyzed by diacylglycerol synthesis (DAG).
16 . Composition according to claim 14 , characterized in that, for at least one of the strains, the acyl transferase can be catalyzed by diacylglycerol synthesis (DAG).
17 . Composition according to one of the preceding claims, characterized in that for at least one of the strains, enzymes catalyse further sugar transfer for the synthesis of microbial peptidoglycans.
18 . Composition according to one of the preceding claims, characterized in that, in the case of at least one of the strains, the expulsion from the cytoplasm is mediated
by a lipoteichonic acid synthesis and/or by a peptidoglycan synthesis
as transporter.
19 . Method for examining the identity of the strains according to one of the preceding claims, characterized in that the effect-mediating genes have a strain-specific pattern of the suppressive subtractive hybridization (SSH).
20 . Method according to claim 19 , characterzied in that the part of
SSH can be determined by pulse field gel electrophoresis.
21 . Use of the composition according to claim, for
preparing a medication or a food supplement or a pharmaceutical preparation
for prophylactic treatment or reduction of the risk of manifestation or for therapy of
eczema and/or
atopic dermatitis and/or
asthma and/or
rhinitis allergica or
other allergies and/or
tuberculosis and/or
colitis ulcerosa and/or
eosinophilic pneumonia and/or
other Th2-driven illnesses or complaints.
22 . Use of the composition according to claim, for
preparing a medication or a food supplement or a pharmaceutical preparation
for prophylactic treatment or reduction of the risk of manifestation or for therapy of
intestinal infections and/or
travel diarrhoea and/or
colds and/or
urogenital infections and/or
HIV-associated complications and complains and/or
candidiasis
or other complaints, infections or other illnesses the defence against which is Th1-mediated.
23 . Use of the composition according to claim, for
preparing a medication or a food supplement or a pharmaceutical preparation
for prophylactic treatment or reduction of the risk of manifestation or for therapy of
rheumatoid arthritis and/or
hashimoto thyreoiditis and/or
uveitis and/or
psoriasis and/or
type 1 diabetes and/or
sjögren disease and/or.
coeliac disease and/or
systemic lupus erythematosus and/or
ankylosing spondylitis and/or
Crohn's disease and/or
inflammatory intestinal diseases and/or
sclerodera and/or
sarcoidosis and/or
multiple sclerosis and/or
vitiligo and/or
Grave's autoimmune thyroiditis and/or
endocrinous opthalmopathy and/or
myasthenia gravis and/or
osteoarthritis and/or
arteriosclerosis and therefore also
cardiac infarction and/or
peripheral arterial occlusive diseases and/or
cerebral infarction (stroke) and/or
metabolic syndrome and therefore also
adipositas and/or
hypertonia and/or
insulin resistance and/or
type 2 diabetes and/or
dyslipoproteinaemia, as well as
amyotrophic lateral sclerosis and/or
interstitial cystitis and/or
irritable bowel syndrome (IBS)
other T helper 1-driven complains and illnesses.
24 . Use of the composition according to claim 6 , for
preparing a medication or a food supplement or a pharmaceutical preparation
for the reduction or elimination of the effects
of autoimmune diseases such as arthritis or dermatitis or
of allergies or
of illnesses with inflammatory components such as a metabolic
syndrome or arteriosclerosis or those complaints and illnesses with inflammatory component mentioned in claim 23 .
25 . Use of the composition according to claims 11 , for
preparing a medication or a food supplement or a pharmaceutical preparation
for the prophylaxis and therapy or osteoporosis by acidification of the milieu and displacement of other microorganisms with the
consequence of better mineral and trace element resorption.
26 . Use of the composition according to claims 11 , for
preparing a medication or a food supplement or a pharmaceutical preparation
for supportive therapy in the case of liver failure and hepatic encephalopathy due to lower resorption of toxins.
27 . Use of the composition according to claims 11 , for
preparing a medication or a food supplement or a pharmaceutical preparation
for the reduction of complaints in the
case of
obstipation and/or
irritable bowel syndrome (IBS) and/or
halitosis.
28 . Use of the composition according to claims 11 , for
Preparing a medication or a food supplement or a pharmaceutical preparation
for reduction of lactose intolerance by improving the lactose exploitation and lactose digestion.
29 . Use of the composition according to claims 11 , for
preparing a medication or a food supplement or a pharmaceutical preparation
and/or for therapy of vaginosis or vaginitis.
30 . Use of the composition according to claims 11 , for
preparing a medication or a food supplement or a pharmaceutical preparation and/or
for intensifying and accelerating the bile acid and cholesterol metabolism.Join the waitlist — get patent alerts
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