WO2007040445A1 - Use of lactobacillus for treatment of virus infections - Google Patents
Use of lactobacillus for treatment of virus infections Download PDFInfo
- Publication number
- WO2007040445A1 WO2007040445A1 PCT/SE2006/001138 SE2006001138W WO2007040445A1 WO 2007040445 A1 WO2007040445 A1 WO 2007040445A1 SE 2006001138 W SE2006001138 W SE 2006001138W WO 2007040445 A1 WO2007040445 A1 WO 2007040445A1
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- WO
- WIPO (PCT)
- Prior art keywords
- lactobacillus
- virus
- use according
- group
- cells
- Prior art date
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P37/08—Antiallergic agents
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
- C12N1/205—Bacterial isolates
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/11—Lactobacillus
- A23V2400/175—Rhamnosus
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
- C12R2001/225—Lactobacillus
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
- C12R2001/225—Lactobacillus
- C12R2001/25—Lactobacillus plantarum
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/853—Lactobacillus
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/853—Lactobacillus
- Y10S435/857—Lactobacillus plantarum
Definitions
- the present invention relates to the use of at least one strain of probiotic bacteria selected from Lactobacillus for the manufacture of a pharmaceutical composi- tion for the treatment and/or prevention of a virus infection .
- Probiotic bacteria are defined as live microorganisms which when administered in adequate amounts beneficially affect the host. Lactobacilli and bifidobacteria are the most frequently used bacteria in probiotic products. These bacteria are generally safe, as are probiotics based on these organisms. The lack of pathogenicity extends across all age groups and to immuno- compromised individuals. Intake of different probiotic bacteria has been shown to have clinical benefits in various physiologic or pathologic situations. The most clear cut effects have been shown in diarrhea caused by antibiotic therapy or rotavirus infection. There are also studies showing positive clinical effects in inflammatory bowel diseases, atopic dermatitis and hypercholesterolemia after intake of probiotic bacteria. The mechanism, by which probiotic bacteria contribute to these clinical improvements are not clear.
- the effects on the innate and acquired immune system following daily in- take of lactobacilli or the Gram-negative bacteria P. lundensis have been thoroughly investigated. Interestingly, it has been observed an activation of the specific cellular immune system in subjects receiving L. plantarum and indications of such in subjects receiving L. paracasei. Moreover, immunity-enhancing effects on the innate immune system, such as expansion of the NKT cell population and increased phagocytic activity were observed in subjects receiving different lactobacilli species. Intake of the Gram-negative bacteria P. lundensis had no effects, whatsoever, on the different immune parameters measured according to the experiments described herein.
- An object of the present invention is the use of at least one strain of probiotic bacteria selected from Lactobacillus for the manufacture of a pharmaceutical compo- sition for the treatment and/or prevention of a virus infection.
- Another object of the present invention is a method for treatment and/or prevention of a virus infection, wherein at least one strain of probiotic bacteria selected from Lactobacillus is administered to an individual .
- Figure 1 shows the numbers of volunteers reporting any minor adverse gastrointestinal effects during the trial.
- Figure 2 shows base line numbers (day 0) of different lymphocytes per ml blood (mean ⁇ (SEM) )
- Figure 3 shows base line (day 0) percentages or GMFI (mean ⁇ (SEM) ) of lymphocytes positive for different cell activation and memory markers .
- FIG. 4 Subjects were randomly assigned to nine different study groups. The trial started with a wash out period of two weeks. Thereafter, the active study period followed. During this period, the subjects consumed one dose of study product per day for 14 (L. plantarum Heal 19, L. fermentum, L. paracasei, L. gasseri, L. rhamnosus, P. lundensis groups) or 35 days (L. plantarum 299v and placebo group) . Each dose contained 10 10 coloni forming units (CFU) [lactobacilli groups) or 10 9 CFU bacteria (P. lundensis group) .
- CFU coloni forming units
- FIG. 1 Percentages of lymphocytes expressing the activation phenotypes CD8CD25, CD8HLA-DR, CD4CD25 and CD4HLA-DR was analysed by flowcytometry .
- FIG. 6 Percentages of lymphocytes expressing the memory phenotypes CD8CD45RO and CD4CD45RO was analysed by flowcytometry. Group means ( ⁇ SEM) based on individual ratios, day 14/day 0 and day 35/day 0 (for L. plantarum and placebo group only) is shown.
- Figure 7. Percentages of lymphocytes positive for the NKT cell markers (CD56CD16CD3) was analysed by flow- cytometry. Group calculations are based on individual ratios (day 14/day 0) .
- Figure 9 shows the ratio of lymphocytes expressing the activation phenotypes CD4CD25 from experiment 2.
- Figure 10 shows the ratio of lymphocytes expressing the activation phenotypes CD4 + CD25 ++ from experiment 2.
- Figure 11 shows the ratio of lymphocytes expressing the activation phenotypes CD8 + HLA-DR + from experiment 2.
- Figure 12 shows the ratio of lymphocytes expressing the activation phenotypes CD8+CD25+ from experiment 2.
- Figure 13 shows the ratio of lymphocytes expressing the activation phenotypes CD4CD45RO from experiment 2.
- the Lactobacillus used according to the invention may be selected from, but not limited to, the group consisting of Lactobacillus plantarum r Lactobacillus rhamnsosus, Lactobacillus fermentum, Lactobacillus para- casei and Lactobacillus gasseri.
- the Lactobacillus plantarum used according to the invention may be selected from, but not limited to, the group consisting of Lactobacillus plantarum 299, DSM 6595, Lactobacillus plantarum 299v, DSM 9843, Lactobacillus plantarum HEAL 9, DSM 15312, Lactobacillus plantarum HEAL 19, DSM 15313, and Lactobacillus plantarum HEAL 99, DSM 15316.
- the Lactobacillus paracasei used according to the invention may be selected from, but not limited to, the group consisting of Lactobacillus paracasei 8700:2, DSM 13434, and Lactobacillus paracasei 02A, DSM13432.
- the Lactobacillus gasseri used according to the invention may be selected from, but not limited to, Lactobacillus gasseri VPG44, DSM 16737.
- Treatable virus infections are i.e. those caused by a virus selected from, but not limited to, the group consisting of herpes simplex I virus, herpes simplex II virus, herpes zoster virus, common cold virus, rhinovirus, adenovirus, parainfluenza virus, respiratory syncytial virus, enterovirus and coronavirus .
- a virus selected from, but not limited to, the group consisting of herpes simplex I virus, herpes simplex II virus, herpes zoster virus, common cold virus, rhinovirus, adenovirus, parainfluenza virus, respiratory syncytial virus, enterovirus and coronavirus .
- Any other virus infection not specifically mentioned here, that the probiotic bacteria have an effect on are also within the scope of the present invention. It is known that there are many different viruses and forms thereof that cause a common cold. All such viruses are within the scope of the present invention.
- treatment and/or prevention includes a prophylactic treatment of an individual, i.e. the treatment with the probiotic bacteria is started before the disease or virus infection has developed in order to prevent the disease/infection, as well as a treatment of a disease/infection that already has developed in an individual.
- a prophylactic treatment of an individual i.e. the treatment with the probiotic bacteria is started before the disease or virus infection has developed in order to prevent the disease/infection, as well as a treatment of a disease/infection that already has developed in an individual.
- an alleviation of the symptoms is for instance expected or the general condition of the patient is enhanced or the patient is cured from the disease/infection faster.
- the individual may be a person at risk for developing an infection or not or an infection has already developed in the patient.
- each of said strain (s) is present in the pharmaceutical composition in an amount of, but not limited to, about IxIO 6 to about IxIO 14 CFU, preferably from about IxIO 8 to about IxIO 12 , and more preferably from about IxIO 9 to about IxIO 11 .
- the pharmaceutical composition according to the invention may e.g. be a liquid formulation or a solid formulation.
- the pharmaceutical composition When the pharmaceutical composition is a solid for- mulation it may be formulated as a tablet, a sucking tablet, a sweet, a chewing tablet, a chewing gum, a capsule, a sachet, a powder, a granule, a coated particle, a coated tablet, an enterocoated tablet, an enterocoated capsule, a melting strip or a film.
- the pharmaceutical composition When the pharmaceutical composition is a liquid formulation it may be formulated as an oral solution, a suspension, an emulsion or syrup. Said composition may further comprise a carrier material independently selected from, but not limited to, the group consisting of oat meal gruel, lactic acid fermented foods, resistant starch, dietary fibres, carbohydrates, proteins, and glycosylated proteins .
- said pharmaceutical composition is a medical food, a functional food, a dietary supplement, a nutritional product or a food preparation .
- the pharmaceutical composition according to the invention, used according to the invention or produced according to the invention may also comprise other sub- stances, such as an inert vehicle, or pharmaceutical acceptable adjuvants, carriers, preservatives etc., which are well known to persons skilled in the art.
- pharmaceutical composition does not necessarily need to be a pharmaceutical composition in its normal sense but may be formulated as a food composition, a dietary supplement, a functional food, a medical food or a nutritional product as long as the required effect is achieved, i.e. treatment or prevention of virus infections .
- Said food composition may be chosen from the group consisting of beverages, yoghurts, juices, ice creams, breads, biscuits, cereals, health bars, spreads and nutritional products.
- the food composition may further comprise a carrier material, wherein said carrier material is chosen from the group consisting of oat meal gruel, lactic acid fermented foods, resistant starch, dietary fibres, carbohydrates, proteins and glycosylated proteins.
- composition according to the invention may be very beneficial in the sense of being usable prophylactically, i.e. before the virus infection has developed. Since the pharmaceutical composition used is not necessarily a pharmaceutical composition in its normal sense, but can also be a dietary supplement or functional food, it is very convenient for a normal healthy individual to take to composition of the invention prophylactically. Examples Example 1 Subjects and trial criteria
- the control group took skim milk powder (1 g) .
- the study had a duration period of 6 or 9 weeks consisting of two weeks wash out period, 2 or 5 weeks active study period and 2 weeks follow up period (Fig. 4) .
- Each subject was supplied with a list of products containing probiotic products, which should not be consumed during the whole study period.
- Peripheral blood samples were withdrawn from subjects by venipuncture at two or three time points, day 0, day 14 and day 35. A diary, in which each subject stated adverse effects, health conditions and confirmed intake of study product, was kept during the trial. Flow cytometry
- Phenotypic analysis of lymphocytes in whole blood was performed by flow cytometry.
- the following anti-human monoclonal antibodies were used as surface markers for different cell populations: CD3 FITC (SK7), CD4 APC (SK3), CD8 PerCP (SKl), CD19 PerCP (SJ25C1) , CD56 PE (MY31), CDl ⁇ PE (B73.1), and CD5 FITC (L17F12).
- CD25 FITC (2A3)
- HLA-DR PE L243
- CD45RO PE UCHL-I
- CD38 PE HB7
- CD27 PE L12
- CDlIb PE D12
- PHAGOTEST ® Orpegen Pharma
- GMFI fluorescence intensity
- NKT cells NKT cells
- Relative increase/decrease compared to day 0 could not be detected regarding other cell populations, such as CD4+ T cells, CD8+ T cells, B cells, B-I cells (CD19+CD5+) , NK cells, granulocytes and monocytes. Phagocytic activity
- the primary task of the immune system is to react rapidly and violently to micro-organisms thereby preventing and curing infections .
- the killing of microorganisms employs , powerful mechanisms that also cause harm to our own tissues. Therefore, it is necessary that it neither reacts to our own tissues, nor to innocuous substances present in the environment. Therefore, the immune system develops and maintains tolerance both to the components of our own body, and to food and inhaled proteins. If this fails, a number of diseases may arise.
- Means to develop specific immune tolerance are an essential task of the immune system.
- T helper cell A central role in all immune reactions is played by the T helper cell.
- a T helper cell When a T helper cell becomes activated by its specific antigen, it becomes activated, divides, matures and produces a range of cytokines which direct the action of other types of cells in the immune system, such as cytotoxic T cells and B cells. Activation of T helper cells is necessary in order to produce most types of immune reactions, including production of antibodies. Conversely, if activation of T helper cells is prevented, most types of immune reactions are paralysed.
- T helper cells There are several mechanisms by which activation of T helper cells and maintenance of tolerance is ensured.
- One mechanism is elimination in the thymus of T cells with capacity to recognize and react to own tissue. However, this elimination is not complete and, furthermore, we also need to develop specific immune tolerance to exogenous antigens. Otherwise we would react violently to all types of inhaled and ingested substances, leading to massive inflammation and wasted immune resources.
- a cell type that is central for maintenance of tolerance is the regulatory T cell.
- This cell type can be recognized by certain markers, such as surface expression of CD4 and CD25, possession of intracellular CTLA-4, and transcription of the nuclear protein Foxp3.
- the regulatory T cells are capable of preventing other T cells to become activated when encountering harmless substances and, hence, prevent all types of unwanted immune reactions .
- the symbol "+" in connection with a certain marker such as CD4+ and CD25+ means that the marker is expressed on a T cell.
- CD4+CD25+ T cells are T cells that expresss both the CD4 marker and CD25 marker on its surface. However, nothing is said about the amount of the marker that is expressed, only that it is present.
- the symbol "++" in connection with a marker such as CD4++ or CD25++ means that there is a lot of marker expressed.
- the regulatory T cells are those cells with a lot of CD25 on the surface, i.e. CD4+CD25++ cells.
- CD4+CD25+ T cells are only activated T cells.
- the specific symbols "+” and "++” are not used, e.g. CD4CD25 only, and this means that the cells are activated such CD4+CD25+ cells.
- CD4CD25 is the same as CD4+CD25+.
- helper T cells after intake of L. plantarum.
- Expression of activation markers indicates that the T cells have started to proliferate in response to antigen- specific or non-specific stimuli and that these cells more readily exert their effector functions compared to resting T cells.
- the mechanisms behind L. plantarum induced activation of T cells could be via antigen presenting cells that are activated by toll-like receptors binding to microbial compounds . Activation of antigen pre- senting cells makes them more efficient in presenting antigen to T cells.
- helper and cytotoxic T cells have shown to have various expressions of toll- like receptors, which probably make these cells sensible for non-specific activation by microbial components and products.
- CD45RO+ T cells can secrete a broad spectrum of cytokines.
- CD45RO+ T cells can proliferate and produce IL-2 when the CD3-TCR complex is stimulated under suboptimal conditions, whereas na ⁇ ve T cells require a strong CD3-TCR stimulus to carry out these functions.
- the formation of memory T cells is important for induction of an efficient immune response after infection and vaccination.
- the innate cellular immune system was also affected by intake of probiotic bacteria. It was demonstrated that the natural killer T (NKT) cell population was expanded following intake of L. paracasei. NKT cells constitute a lymphocyte subpopulation that coexpress the NK cell marker CD56 and the T cell marker CD3-T cell receptor complex.
- NKT cells play a central role in the regulation of autoimmune diseases, such as multiple sclerosis, type I diabetes, and systemic lupus. NKT cells also exert effector functions against tumour and virus infected cells. Thus, NKT cells are pleotropic in their functions.
- Other clinical studies evaluating the immunological effects of probiotic bacteria have shown that intake of L. rhamnosus HNOOl and Bifidobacterium lactis HN019 enhance NK (including NKT) cell tumour killing activity of K562 cells. In this study it was also confirmed the observation by others that phagocytic activity of polymorphonuclear cells is increased after intake of different lacto- bacilli .
- the goal of this example was to investigate the ef- feet on the immune system by giving the same species of lactobacilli for a longer period of time compared to several lactobacilli (different species) administered in a sequence one after the other.
- gram-positive bacteria the probiotic bacteria Lactobacillus plantarum 299v is used alone or in combination with L. rhamnosus, L. fer- mentum, L. paracasei, and L. gasseri.
- gram-negative bacteria Psedomonas lundensis is given.
- Control group 2 Placebo 14 days Blood samples are taken at day 0, 14 and 35.
- the amount of helper T cells (CD4+) expressing high amounts of CD25 was defined in each group by flow cytometry as have been explained above in experiment 1.
- the aim of the present study is to investigate whether intake of the lactic acid bacteria in a freeze- dried formula/functional food product during at least 3 months influences the severity of symptoms and the incidence and duration of common cold.
- the study will take place during 90 days and 500 in- dividuals will take part in the study. 250 individuals will receive the active product and 250 individuals will be given a placebo. The study will be randomized, double blind and placebo-controlled with two parallel arms .
- Exclusion criteria are as follows : Known intolerance or allergy to any ingredient included in the formula- tions; allergy medically treated; Current treatment for severe gastrointestinal disorders; Pregnancy or lactation; Vaccination against influenza within the last 12 months; and smokers.
- Each sachet will be labelled with the name of the study, the best by date, how they are to be stored, the name of the manufacturer, the name of the responsible investigator and her/his telephone number.
- a number denoting the subject is added on the secondary package.
- a detailed instruction for dissolution and intake will be inserted in the secondary package.
- the prod- uct will be supplied in sachets.
- the subject may not ingest products containing probiotic bacteria.
- the subject will be provided with a list of probiotic products not allowed to be consumed during the study period. Faecal samples are to be handed in on days 1 (before intake of study product) , 15 (after intake) , and 104 (after intake) .
- the samples should be collected in two tubes no more than 18 hours before being handed in for analysis, and during this period are to be stored in a refrig- erator.
- the samples will be analysed for lactobacilli .
- Blood samples are to be taken day 1 and 15. The samples will be analyzed for CD4+ and CD8+. In view of experiments 1 and 2 it is expected that an enhanced protection against common cold will be seen in the individuals taking the probiotic mixture compared to the placebo group.
Abstract
Description
Claims
Priority Applications (14)
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EP06799738.7A EP1951272B1 (en) | 2005-10-06 | 2006-10-06 | Use of lactobacillus for treatment of virus infections |
JP2008534490A JP5792919B2 (en) | 2005-10-06 | 2006-10-06 | Use of lactic acid bacteria for the treatment of viral infections |
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US13/619,146 US8691214B2 (en) | 2005-10-06 | 2012-09-14 | Use of Lactobacillus for treatment of virus infections |
CY20161100908T CY1118006T1 (en) | 2005-10-06 | 2016-09-13 | USE OF Lactobacilli For The Treatment Of Viral Infections |
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WO2012133827A1 (en) * | 2011-03-31 | 2012-10-04 | 森永乳業株式会社 | Novel lactic acid bacterium, and pharmaceutical, food or drink, and feed, each containing novel lactic acid bacterium |
WO2014038929A1 (en) | 2012-09-07 | 2014-03-13 | N.V. Nutricia | Probiotics for producing antiviral factors |
US8679558B2 (en) | 2009-05-14 | 2014-03-25 | Probi Ab | Probiotic juice drink |
WO2014072594A1 (en) * | 2012-11-09 | 2014-05-15 | Institut National De La Recherche Agronomique (Inra) | Novel lactobacillus plantarum bacterial strain and uses of this strain |
US8809342B2 (en) | 2010-12-23 | 2014-08-19 | Pfizer Inc. | Glucagon receptor modulators |
US8859591B2 (en) | 2011-02-08 | 2014-10-14 | Pfizer Inc. | Glucagon receptor modulators |
US8927577B2 (en) | 2011-07-22 | 2015-01-06 | Pfizer Inc. | Quinolinyl glucagon receptor modulators |
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