WO2008057160A2 - Compositions and multiplex assays for measuring biological mediators of physiological health - Google Patents
Compositions and multiplex assays for measuring biological mediators of physiological health Download PDFInfo
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- WO2008057160A2 WO2008057160A2 PCT/US2007/021451 US2007021451W WO2008057160A2 WO 2008057160 A2 WO2008057160 A2 WO 2008057160A2 US 2007021451 W US2007021451 W US 2007021451W WO 2008057160 A2 WO2008057160 A2 WO 2008057160A2
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
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- A61P3/00—Drugs for disorders of the metabolism
- A61P3/02—Nutrients, e.g. vitamins, minerals
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- A61P3/00—Drugs for disorders of the metabolism
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- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
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- C—CHEMISTRY; METALLURGY
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- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/158—Expression markers
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- G—PHYSICS
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- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/04—Endocrine or metabolic disorders
Definitions
- This invention relates generally to facile assays for determining the health status of animals and particularly to multiplex assays involving the measurement of cytokines, hormones, and adipokines to access animal health status and the effect of nutrition on health status
- Cytokines, adipokines, and hormones are among the principal biological mediators orchestrating physiological response to stimuli and stress and are therefore useful as 'signatures' of health status and/or indicators of disease Evaluating changes, both static and temporal, in these mediators provides some understanding of the response of a biological system or organism to stressors
- the set of analytes comprise at least one cytokine or gene therefor, one chemokine or gene therefor, one hormone or gene therefor, and one adipokine or gene therefor and, for each analyte in the set, the collection of molecular probes comprises at least one probe suitable for detecting the activity, presence, or expression of that analyte
- the set of analytes further comprises one or more neuronal growth factors or genes therefor, growth factors other than neuronal growth factors or genes therefor, soluble receptors or genes therefor, or combinations thereof
- Figure 1 Diagrammatic presentation of Metabolic Syndrome showing the central role that insulin resistance holds and ultimate risk of heart disease, stroke, and/or inflammation
- FIG. 1 Cytokines response to LPS stimulation PBMCs were cultured with different cone of LPS for 3, 6, or 18 hrs C/S were assayed for cytokines Data for IL-6 [A], TNF ⁇ [B], IL-18 [C] and IL-8 [D] are shown X-axis LPS dose ng/ml, Y-axis is Mean Fluorescence Intensity [MFI] or [MF] and Z-axis represents time-point
- the term "activity" of a gene encompasses any measure that it is related to the central biological roles played by a gene For example, measurement of the transcription of a gene, or measure either at static time points or in real time of the abundance of an RNA species transcribed therefrom
- a measure of a gene's "activity” as used herein can also include measurements in specific tissues, cell-types, or organs, of the amount of mRNA produced from a particular gene, whether in real time or not
- protein analytes can be measured in a variety of useful ways Measurement of protein and other analytes can include the presence or absence of the analyte, activity (e g enzyme activity or other biological activity), binding properties, half-life, turn-over, or other measurable attributes of the analyte
- analyte includes proteins "expressed from a gene” in the form of native proteins as they are translated in the cell and proteins having post-translational tranlocation, processing, modifications, and the like Thus, in some cases protein analytes may be truncated after translation, or for example may be phosphorylated, or have other modifications such as to the backbone or to the side chain of any amino acid residue
- analyte also includes metabolic derivatives of such proteins, and complexes, whether active or not, of one or more proteins with one or more other substituents found in a cell
- the analytes are protein or peptides and the probes are antibodies Each antibody in the collection of probes specifically recognizes only one protein in the set, and there is at least one such antibody in the collection for each protein in the selected set.
- animal means any animal having cytokines, hormones, adipokines, neuronal growth factors, growth factors other than a neuronal growth factors, or soluble receptors useful in the present invention, including, but not limited to, human, avian, bovine, canine, equine, feline, hic ⁇ ne, murine, ovine, and porcine animals, preferably humans, murines simians, canines, and felines
- selection in referring to a group of molecular probes means a plurality Typically the plurality has no limit, although collections of 100 or fewer probes are preferred
- molecular probe(s) means any molecule that can be used to detect the presence or activity of a gene, its corresponding RNA, or its protein expression product
- a collection as used herein is preferably, but not necessarily, used for detecting a corresponding set of analytes in multiplex fashion, i e , all of the results for each of the plurality of probes are obtained from a single reaction or assay vessel
- a collection of probes typically corresponds to a set of analytes, wherein each of the plurality of probes corresponds to a particular analyte in the set
- the analytes are genes or gene products (proteins) and the probes allow the measurement of the activity or expression of each of the genes (or their expression products) in the group (or set) More preferably, the analytes are proteins expressed from the gene
- single package means that the components of a kit are physically associated in or with one or more containers and considered a unit for manufacture, distribution, sale, or use
- Containers include, but are not limited to, bags, boxes, bottles, shrink wrap packages, stapled or otherwise affixed components, or combinations thereof
- a single package may be containers of individual assay components physically associated such that they are considered a unit for manufacture, distribution, sale, or use
- kits are associated by directions on one or more physical or virtual kit components instructing the user how to obtain the other components, e g , in a package containing one component and directions instructing the user to go to a website, contact a recorded message, view a visual message, or contact a caregiver or instructor to obtain instructions on how to use the kit
- the present invention provides a collection of detectable molecular probes for determining in a single sample, the activity, presence, or expression of each of a predetermined set of analytes
- the set of analytes comprises at least one cytokine or gene therefor, one chemokine or gene therefor, one hormone or gene therefor, and one adipokine or gene therefor
- the collection of molecular probes comprises at least one probe suitable for detecting the activity, presence, or expression of that analyte
- the molecular probes comprise protein, nucleic acid, or combinations thereof but may comprise small molecules or other compounds and structures or combinations thereof
- probes comprising protein include antibodies, antibody fragments, receptors, binding proteins, enzymes, and the like They may be used to probe for not only protein analytes, but a variety of other analytes
- Nucleic acid probes include those whose specificity arises through complementary Watson-C ⁇ ck-type base-pairing, as well as those whose specificity arises from or includes other interactions
- aptamers, nucleic acids that can be designed to specifically recognize certain analytes, such as proteins or other molecules are useful herein
- Nucleic acid enzymes such as DNAzymes and ⁇ bozymes are known in the art, have known specificities, and are useful as probes herein
- Probes may also comprise ligands for binding molecules and receptors The use of all such molecules as probes for analytes, such as the expression products of genes, or even the genes themselves, is known in the art,
- Probes can be man-made or isolated from nature
- the molecular probes are antibodies
- each antibody in a collection can specifically recognize and thus serve to identify, one protein analyte in a corresponding set of proteins
- Probes may be used in any convenient format, such as in solution or suspension
- they may bound to a substrate, such as a carrier or a bead, or placed in an array, microarray, or the like so as to create a useful, convenient, and/or informative assay system
- the predetermined set of analytes in certain embodiments is a set of genes, or a set or proteins
- a set of protein analytes is selected and assays based on a corresponding set of genes or mRNAs are developed
- the set of analytes is selected on a rational basis, based on its relationship to the information to be obtained from the panel
- the set of analytes is selected based on the relationship of each analyte to the health status of an individual
- the set of analytes is a set of proteins comprising at least one cytokine, one chemokine, one hormone, and one adipokine
- the collection of molecular probes comprises at least one probe suitable for detecting the presence, activity or expression of that analyte - i e there is a corresponding probe for each analyte in the set whose presence, activity, or expression is to be determined
- the collection of molecular probes is the foregoing set of protein analytes
- the set of analytes further comprises one or more of at least one other type of probiotic organism
- the set of analytes comprises a set of genes with at least one gene encoding a cytokine, one gene encoding a chemokine, one encoding a hormone, and one, an adipokine
- the set of gene analytes further comprises at least
- an upper limit is 100 probes per collection in certain embodiments Smaller collections of probes are also suitable For example panels of about 90-100, 80-90, 70-80 or 60-70 probes are all suitable for use herein Similarly, collections of about 10-20, 20-30, 30-40, 40-50 or 50-60 are also suitable for use Other specific numbers of probes from 4 to 100 are also included herein, although not specifically enumerated, as are all possible ranges of from 4-100 probes included herein, though not specifically enumerated Ranges of probes are particularly useful where some redundancy may be initially desirable, and later found to be unnecessary, or alternatively, where an additional probe may be determined to be useful to include with a particular collection as more about its role in vivo is discovered or appreciated In other embodiments, for example where the probes may be bound to an array or microarray, it may be useful, and thus preferable, to exceed 100 probe
- the collection of molecular probes comprises detectable probes for detecting a protein (i e , an encoded gene product) of each of a set of genes thereby determining the expression of each gene in the set
- each probe is specific for detecting the encoded protein for one gene in the set
- a degree of cross-reactivity may be experimentally acceptable This is particularly true where the probes are themselves biological molecules, such as antibodies
- the cross-reactivity of certain antibodies is recognized in the art The skilled artisan will appreciate that cross-reactivity of antibodies to closely-related antigens, such as some proteins can create problems, especially if severe
- the cross-reactivity is minimized or eliminated through the use of monospecific antibodies, such as highly-purified antibodies, or monoclonal antibodies to specific epitopes that are immunologically distinguishable
- the cross-reactivity is distinguishable from the intended activity based on binding properties such as binding constants, or a measure of binding strength, or the like
- the cross-reactivity is distinguishable from the intended activity based on binding properties such as binding
- the set of analytes While there are many choices for the set of analytes, as discussed herein, a rational approach to the selection of analytes is preferred
- the collection of molecular probes will preferably be designed or selected with the goal of the intended use in mind
- the set of analytes is predetermined via a rational approach which rests on the known, predicted, or herein discovered relationships between the presence or activity of certain analytes to various aspects of health of an animal Factors such as the state of inflammation in an animal and the relative presence of certain hormones and other biochemical signals or signal conductors can help to provide detailed information linked to the health status of an animal
- the set of analytes is a set of proteins that comprises one or more cytokines
- the cytokine includes one or more of interferon alpha, interferon gamma, interleukin 12 p40, interleukin 18, interferon beta, interferon omega, lymphotoxin beta R, lymphotoxin, interleukin 6, interleukin 8, tumor necrosis factor alpha, interleukin 4, interleukin 10, transforming growth factor beta-1 , tumor necrosis factor beta, interleukin 3, interleukin 5, interleukin 7, interleukin 13, interleukin 15, interleukin 1 alpha, interleukin 1 beta, interleukin 2, interleukin 1 1 , interleukin 12 p70, interleukin 16, interleukin 17, Regulated upon Activation, Normal T Expressed and presumably Secreted (RANTES), interleukin 21, interleukin 9, or transforming growth factor beta receptor III
- RANTES Normal T Expressed and presumably Secret
- the set of proteins comprises one or more chemokines, for example, B- lymphocyte chemoattractant, epithelial cell-derived neutrophil-activating peptide, eotaxin, eotaxin-2, monocyte chemotactic protein 2, monocyte chemotactic protein 3, macrophage migration inhibitory factor, macrophage inflammatory protein 1 alpha, myeloid progenitor inhibitory factor 1 , macrophage stimulating protein, granulocyte chemotactic protein 2, interferon gamma inducible protein 10, leukemia inhibitory factor, macrophage colony stimulating factor, monocyte chemotactic protein 1, macrophage-de ⁇ ved chemokine, macrophage inflammatory protein 1 beta, macrophage inflammatory protein 1 delta, neutrophil activating peptide 2, pulmonary- and activation-regulated chemokine, stromal cell-derived factor alpha, thymus- and activation-regulated chemokine, betacellulin, 6 Ckine,
- chemokines for example,
- the set of proteins comprises one or more hormones
- other hormones may be selected
- the activity or the presence of the hormones is affected by a selected nutritional regimen as discussed below, or there is a relationship between the activity or presence of the hormone to the health status of an animal
- the inclusion of certain hormones does not preclude and may be in addition to the inclusion of other molecules for example cytokines, chemokines, adipokines, and others described herein
- the set of proteins comprises one or more adipokines, including but not limited to monocyte chemotactic protein 1 , leptin, resistin, adiponectin, IL-6, TNF-alpha, or thrombin- activatable fibrinolysis inhibitor
- the predetermined set of protein analytes further comprises one or of a neuronal growth factor, a growth factor other than a neuronal growth factor, or a soluble receptor, or combinations thereof
- Neuronal growth factors for use herein include but not limited to ciliary neurotrophic factor, glial cell line derived neurotrophic factor, brain-derived neurotrophic factor, neurotrophin 3, neurotrophin 4, or beta- nerve growth factor
- the set of genes comprises, in certain embodiments, one or more genes encoding one or more chemokines B-lymphocyte chemoattractant, epithelial cell-derived neutrophil-activating peptide, eotaxin, eotaxin-2, monocyte chemotactic protein 2, monocyte chemotactic protein 3, macrophage migration inhibitory factor, macrophage inflammatory protein 1 alpha, myeloid progenitor inhibitory factor 1 , macrophage stimulating protein, granulocyte chemotactic protein 2, interferon gamma inducible protein 10, leukemia inhibitory factor, macrophage colony stimulating factor, monocyte chemotactic protein 1 , macrophage-de ⁇ ved chemokine, macrophage inflammatory protein 1 beta, macrophage inflammatory protein 1 delta, neutrophil activating peptide 2, pulmonary- and activation-regulated chemokine, stromal cell-derived factor alpha, thymus- and activation-regulated chemokine, betacellulin
- the set of genes comprises one or more genes encoding various hormones
- genes encoding the hormones prolactin, insulin-like growth factor binding protein 2, leptin, insulin, resistin, adiponectin, glucagon, glucagon-related peptide 1 , or PYY
- the inclusion in the set of analytes of one or more genes encoding hormones does not preclude the inclusion of one or more genes encoding other molecules, for example, cytokines, chemokines, adipokines, and others described herein
- the set of genes comprises one or more genes encoding one or more of the adipokines monocyte chemotactic protein 1, leptin, resistin, adiponectin, IL-6, TNF-alpha, or thrombin- activatable fibrinolysis inhibitor Genes for other
- the predetermined set of genes further comprises one or more genes encoding a neuronal growth factor, a growth factor other than a neuronal growth factor, or a soluble receptor
- a neuronal growth factor a growth factor other than a neuronal growth factor
- soluble receptors include but are not limited to those enumerated herein for the set of proteins Other such molecules are also contemplated for use herein
- the set of analytes comprises one or more primary or secondary metabolic products
- the set of analytes includes one or more eicosanoids, a class of oxygenated hydrophobic molecules that largely function as autocrine and paracrine mediators of biological functions
- leukot ⁇ enes are known to serve as agents in the inflammatory response Some have a chemotactic effect on migrating neutrophils, and as such help to bring necessary cells to the involved tissue
- Leukot ⁇ enes also are powerful vasoconstrictors, particularly of venules They function in bronchoconst ⁇ ction, and can also increase vascular permeability
- Leukot ⁇ enes suitable for use herein include but are not limited to LTA4, LTB4, LTC4, LTD4, LTE4, and LTF4
- Other eiscosanoids suitable as analytes for use herein include thromboxanes and the prostaglandin H derivatives, prostanoids Still other eiscosanoid
- the collection of molecular probes comprise probes using canine specific molecules suitable for producing for a canine assay Panel, Cytokine / chemokine, Analyte GMCSF, IL-2, IL-4, IL-6, IL-7, IL-8, IL-10, IL-18, IFN ⁇ , IP-10, TNF- ⁇ , MCP-I , IL- 15, KC Panel, Endocrine, Analyte GLP-I , Glucagon, Insulin, Leptin Panel, Adipokine, Analyte Adiponectin, Resistin
- the collection of molecular probes comprise probes using feline molecules suitable for producing a feline assay Panel, Cytokine / chemokine, Analyte GMCSF, IL-2, IL-4, IL-6, IL-l ⁇ , IL-8, IL- 10, IL-18, IFN ⁇ , Fas, TNF- ⁇ , MCP-I , Flt-3
- the molecular probes are capable of detecting the presence, activity, expression, or the like of each of the analytes in the predetermined set of analytes
- the set of analytes are the sets of proteins and/or genes set forth herein More preferably the genes are from a human, a simian, a canine, or a feline
- the collection of probes is specific for detecting the presence or activity of a set of canine or feline proteins
- the collection of molecular probes is a plurality of antibodies specific for measuring or detecting protein analytes (i e the expression products from a set of genes) from a canine
- the probes provide a quantitative determination of the amount of expression of each protein, such as the amount of each specific protein present in the sample
- the results are more qualitative providing information as to relative amounts, for example indicating differences or changes from sample to sample, or changes over a time course in samples from an individual
- analogous measurements are obtain for the set of genes corresponding to the selected proteins
- each probe is attached to a matrix, or support, wherein each such attached probe remains capable of providing a quantitative determination of the amount of activity or presence of each of a set of analytes in a sample brought into contact with the matrix
- probes of the type described herein can be attached, immobilized, or supported in a variety of ways to allow
- Adiponectins MCP- I Monocyte Chemotactic Protein 1 Leptin, Leptin Resistin, Resistin Adiponectin, Adiponectin IL-6, IL-6 TNF- ⁇ , TNF-alpha and tPAI- 1 , thrombin-activatable fibrinolysis inhibitor
- Neuronal Growth Factors CNTF, Ciliary neurotrophic factor GDNF, Glial cell line derived neurotrophic factor BDNF, Brain-derived neurotrophic factor NT-3, Neurotrophin 3 NT-4, Neurotrophin 4 and ⁇ -NGF, beta-Nerve Growth Factor
- Growth Factors ANG Angiogenin EGF, Epidermal growth factor FGF-7, Fibroblast growth factor-7 FGF-9, Fibroblast growth factor-9 GM-CSF, Granulocyte macrophage colony stimulating factor GRO- ⁇ (MGSA), (CXCLl), Melanoma Growth Stimulating Activity OSM, Oncostatin M PlGF, Placenta growth factor TGF- ⁇ 3, Transforming growth factor beta-3 AR, Amphiregulin FGF-6, Fibroblast growth factor-6 G-CSF, Granulocyte colony stimulating factor SCF, Stem cell factor VEGF, Vascular endothelial growth factor CT-I , Cardiotrophin- 1 GRO- ⁇ , (CXCL2), Growth Related Oncogene beta HB-EGF, Hepa ⁇ n- Binding EGF-like Growth Factor HGF, Hepatocyte growth factor HVEM, (TNFRSF14), Herpesvirus Entry Mediator MMP-10 (total), Matrix Metalloproteinase 10 MMP
- the invention provides methods of assessing the health status of an animal by determining the relative activity or expression of a set of analytes Generally, the methods comprise the steps of a) obtaining a biological sample from the animal, where the sample at least putatively contains a predetermined set of analytes of interest
- the set of analytes comprises at least one cytokine, chemokine, hormone, and adipokine b) contacting the sample with a collection of molecular probes for determining the activity or presence of each of the predetermined set of analytes, wherein for each analyte in the set, the collection of molecular probes comprises at least one probe suitable for detecting the presence or a measurable activity of that analyte
- Each probe in the collection is capable of producing an independently detectable signal when the analyte corresponding to that probe is present in the sample c) detecting the independently detectable signals produced after the sample is contacted with the collection d) correlating the detectable signals with at least
- the set of analytes comprises and set of genes and the method comprises the steps of a) obtaining a biological sample from the animal, where the sample at least putatively contains a predetermined set of genes of interest or the expression products of those genes
- the set of genes comprises at least one gene each encoding a cytokine, a chemokine, a hormone, and an adipokine b) contacting the sample with a collection of molecular probes for determining the activity or expression of each of the predetermined set of genes, wherein for each gene in the set, the collection of molecular probes comprises at least one probe suitable for detecting the activity or expression of that gene
- Each probe in the collection is capable of producing an independently detectable signal when the gene or expression product of the gene corresponding to that probe is present in the sample c) detecting the independently detectable signals produced after the sample is contacted with the collection d) correlating the detectable signals with at least the relative activity or expression of each of the predetermined set of genes in the sample, e
- the set of analytes further comprises one or more of a neuronal growth factor, a growth factor other than a neuronal growth factor, or a soluble receptor, in addition to the cytokine, chemokine, hormone, and adipokine discussed herein
- the analytes are genes
- the set comprises the corresponding genes, in accordance with the foregoing limitations
- the detectable probes are specific for detecting a the presence or activity of each of the proteins (or encoded gene product of each of the set of genes), or the activity or expression of each of the genes
- the detectable probes comprise antibodies, antibody fragments, ligands, receptors, or binding proteins, nucleic acids, for example DNA or RNA
- the set comprises the proteins
- the collection of probes comprises antibodies for each of the proteins
- the set of proteins or genes comprises one or more genes encoding, or proteins which are the cytokines interferon alpha, interferon gamma, interleukin 12 p40, interleukin 18, interferon beta, interferon omega, lymphotoxin beta R, lymphotoxin, interleukin 6, interleukin 8, tumor necrosis factor alpha, interleukin 4, interleukin 10, transforming growth factor beta-1 , tumor necrosis factor beta, interleukin 3, interleukin 5, interleukin 7, interleukin 13, interleukin 15, interleukin 1 alpha, interleukin 1 beta, interleukin 2, interleukin 1 1 , interleukin 12 p70, interleukin 16, interleukin 17, Regulated upon Activation, Normal T Expressed and presumably Secreted (RANTES), interleukin 21 , interleukin 9, or transforming growth factor beta receptor III
- RANTES Normal T Expressed and presumably Secreted
- the predetermined set of analytes may, alternatively or in addition to the foregoing, include one or more proteins which are or genes encoding the chemokines B-lymphocyte chemoattractant, epithelial cell-derived neutrophil-activating peptide, eotaxin, eotaxm-2, monocyte chemotactic protein 2, monocyte chemotactic protein 3, macrophage migration inhibitory factor, macrophage inflammatory protein 1 alpha, myeloid progenitor inhibitory factor 1, macrophage stimulating protein, granulocyte chemotactic protein 2, interferon gamma inducible protein 10, leukemia inhibitory factor, macrophage colony stimulating factor, monocyte chemotactic protein 1, macrophage-de ⁇ ved chemokine, macrophage inflammatory protein 1 beta, macrophage inflammatory protein 1 delta, neutrophil activating peptide 2, pulmonary- and activation-regulated chemokine, stromal cell-derived factor alpha, thymus
- the predetermined set of genes or proteins may also include one or more genes encoding or proteins which are the adipokines monocyte chemotactic protein 1 , leptin, resistin, adiponectin, IL- 6, TNF-alpha, or thrombin-activatable fibrinolysis inhibitor
- the predetermined set of genes or proteins further variously comprises one or more genes encoding one or more of the following, or the proteins themselves the neuronal growth factors ciliary neurotrophic factor, glial cell line derived neurotrophic factor, brain-derived neurotrophic factor, neurotrophin 3, neurotrophin 4, or beta-nerve growth factor, the growth factors angiogenin, epidermal growth factor, fibroblast growth factor-7, fibroblast growth factor-9, granulocyte macrophage colony stimulating factor, melanoma growth-stimulating activity, oncostatin M, placenta growth factor, transforming growth factor beta-3, amphiregulin fibroblast growth factor-6, granulocyte colony stimulating factor, stem cell factor, vascular endothelial growth factor, cardiotrophin- 1 , growth-related oncogene beta, hepa ⁇ n-binding EGF-like growth factor, hepatocyte growth factor, herpesvirus entry mediator, matrix metalloproteinase 10, matrix metallo
- the predetermined set of analytes comprises one or more of genes encoding each, of IL-2, IL-4, IL-6, IL-7, IL-8, IL-10, IL- 18, IFN ⁇ , IP-10, TNF- ⁇ , MCP-I , GLP- I , glucagon, insulin, adiponectin, and resistin
- the set of analytes comprises the foregoing proteins themselves
- the animal is human, murine, simian, canine, or feline
- the predetermined set of analytes further comprises one or more genes encoding IL- 15, KC, or leptin, or the proteins themselves, in certain embodiments
- the analytes are from a canine and the probes are antibodies specific for the proteins or expression products of the genes encoding them.
- the collection of molecular probes allow for a quantitative determination of the amount of the protein, or the expression of each gene
- each probe attached to a matrix, wherein each such attached probe remains competent to provide a quantitative determination of the amount of expression of a gene corresponding to that probe, in a sample brought into contact with the matrix
- the method further comprises a step of contacting the sample and the collection of molecular probes with a set of secondary antibodies comprising one or more antibodies that can, for example, detect the presence of a particular portion or type of an antibody, detect specific binding between an expression product of each gene in the set, and a corresponding probe in the collection
- a set of secondary antibodies comprising one or more antibodies that can, for example, detect the presence of a particular portion or type of an antibody, detect specific binding between an expression product of each gene in the set, and a corresponding probe in the collection
- either the probe or a second antibody can be further linked to a signal generation or amplification system, such as an enzyme
- the methods in certain embodiments involve the use of a collection of molecular probes wherein each probe is attached to a separate matrix, such as a bead or a polymeric support material
- the methods involve the use of a biological sample, which is preferably a sample which is likely to contain the genes in the predetermined set, or is likely to contain the expression products thereof, is easy and relatively painless to obtain, is abundant or whose absence will do the animal no harm, and is reproducible
- samples include blood, serum, plasma, urine, tissue extracts, cerebral spinal fluid (CFS), synovial fluid, and cellular extracts Tissue culture cells, extracts, supernatant fluids, and spent culture medium are also useful herein
- Preferred samples are blood, serum, and plasma Sample size is not critical, samples can be of any size that is useful, practical, and analytically meaningful Samples of less than 1 ml are preferred Samples typically are less than 100 ⁇ l, for example 75 or 50 ⁇ l Smaller samples are also useful herein Sample that are sufficiently small to allow assays in standard laboratory equipment, are of course preferred, as are miniaturized assays
- the invention provides methods of formulating a nutritional regimen for improving the health of an animal
- the methods comprise a) selecting a predetermined set of analytes of interest in an animal wherein the activity of the analytes, or presence thereof can be correlated with the health status of the animal, and with a nutritional regimen of the animal, the set comprising at least one protein or one gene encoding each of a cytokine, a chemokine, a hormone, and an adipokine, b) obtaining a biological sample from the animal, said sample putatively containing the predetermined set of analytes, or the expression products thereof, said sample indicative of a current nutritional regimen of the animal, c) determining a baseline measurement by contacting the sample with a collection of molecular probes for determining the activity or presence of each of the predetermined set of analytes, or expression product thereof, wherein for each analyte in the set, the collection of molecular probes comprises at least one probe suitable for detecting the
- step j) refers to repeating steps b) through g) however these steps are repeated with a new sample taken from the animal after step j), i e , after the animal has received the new nutritional regimen
- the selection of the predetermined analytes is essentially a rational process of selecting those analytes, the presence, activity, or expression of which can be correlated with both health status and a nutritional regimen, and which will provide useful results Selection of analytes that have zero correlation with health status and zero correlation any nutritional regimen is to be avoided, although such analytes may be included as controls or test analytes, or the like [0077]
- the methods described herein are useful for the formulation of any nutritional regimen with any animal as described herein In various preferred embodiments, the methods are quite useful in situations wherein the animal is obese, has diabetes, has symptoms of being predisposed to diabetes, has an undesirable level of inflammation, has an undesirable level of insulin resistance, has metabolic syndrome, premature atherosclerosis, abnormal glucose metabolism, or abnormal fat metabolism Many such conditions are known in the art and can be loosely or more strictly associated with nutritional regimens, particularly long-term nutritional regimens In one embodiment, the formulated nutritional regimen, supplement, or combination thereof improves the immune function,
- the predetermined set of analytes comprises one or more genes encoding each of IL-2, IL-4, IL-6, IL-7, IL-8, IL- I O, IL- 18, IFN ⁇ , IP- 10, TNF- ⁇ , MCP-I , GLP- I, glucagon, insulin, adiponectin, and resistin, or the corresponding proteins Additionally, one or more genes encoding IL- 15, KC, or leptin may be included, or the corresponding proteins
- the animal is human, murine, simian, canine, or feline
- the analytes are proteins from a canine and the molecular probes are antibodies that allow for a quantitative determination of the amount of such proteins
- each probe is attached to a matrix and remains capable of providing a quantitative determination of the amount of the analyte corresponding to that probe when a sample contacts the matrix
- the methods can also comprise the further step of contacting the sample and the collection of molecular probes with a set of secondary probes, e g , secondary antibodies comprising one or more antibodies that increase specificity or increase signal through amplification
- a set of secondary probes e g , secondary antibodies comprising one or more antibodies that increase specificity or increase signal through amplification
- each probe is attached to a separate matrix
- the sample can be any biological sample such as tissue or bodily fluid
- kits suitable for determining in a single sample, the activity, presence, or expression of each of a predetermined set of analytes comprise in separate containers in a single package or in separate containers in a virtual package, as appropriate for the kit component, a multiplex assay comprising a collection of detectable molecular probes as defined herein and one or more of
- the kit comprises the multiplex assay and a food composition such as a nutritionally complete food for pets or nutritional supplements such as vitamins and minerals that are useful for formulating a nutritional regimen for improving the health of an animal
- the kit comprises a virtual package
- the kit is limited to instructions in a virtual environment in combination with one or more physical kit components
- the kit may contain additional items such as a device for mixing reagents useful with the multiplex assay or a device for supporting and/or handling the multiplex assay
- the present invention provides a means for communicating information about or instructions for using the multiplex assay for one or more of ( 1) determining in a single sample, the activity, presence, or expression of each of a predetermined set of analytes, (2) assessing the health status of an animal, or (3) formulating a nutritional regimen for improving the health of an animal
- the means comprises a document, digital storage media, optical storage media, audio presentation, or visual display containing the information or instructions
- the communication means is a displayed web site, visual display kiosk, brochure, product label, package insert, advertisement, handout, public announcement, audiotape, videotape, DVD, CD-ROM, computer readable chip, computer readable card, computer readable disk, computer memory, or combination thereof containing such information or instructions
- Useful information includes one or more of (1) methods and techniques for handling biological samples for use with the multiplex assay (2) contact information for Indie duals to use if they have a question about the multiplex assay and its use [0086]
- the invention is not limited to the particular methodology
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Abstract
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Priority Applications (10)
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EP07867209A EP2069524A4 (en) | 2006-10-06 | 2007-10-04 | Compositions and multiplex assays for measuring biological mediators of physiological health |
US12/311,542 US20100196880A1 (en) | 2006-10-06 | 2007-10-04 | Compositions and multiplex assays for measuring biological mediators of physiological health |
MX2009003583A MX2009003583A (en) | 2006-10-06 | 2007-10-04 | Compositions and multiplex assays for measuring biological mediators of physiological health. |
BRPI0717803-4A BRPI0717803A2 (en) | 2006-10-06 | 2007-10-04 | COMPOSITIONS AND MULTIPLIER TESTS FOR THE MEASUREMENT OF BIOLOGICAL PHYSIOLOGICAL HEALTH MEDIATORS |
CA002665164A CA2665164A1 (en) | 2006-10-06 | 2007-10-04 | Compositions and multiplex assays for measuring biological mediators of physiological health |
AU2007318208A AU2007318208B2 (en) | 2006-10-06 | 2007-10-04 | Compositions and multiplex assays for measuring biological mediators of physiological health |
RU2009116433/10A RU2520080C2 (en) | 2006-10-06 | 2007-10-04 | Compositions and multi-parameter assays for measuring biological mediators of physiological health |
CN200780037405.0A CN101627129B (en) | 2006-10-06 | 2007-10-04 | Compositions and multiplex assays for measuring biological mediators of physiological health |
JP2009531477A JP2010505420A (en) | 2006-10-06 | 2007-10-04 | Compositions and multiplex assays for measuring biological mediators of physiological health |
US13/296,751 US20120122717A1 (en) | 2006-10-06 | 2011-11-15 | Composition and multiplex assays for measuring biological mediators of physiological health |
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JP2010075121A (en) * | 2008-09-26 | 2010-04-08 | National Institute Of Advanced Industrial Science & Technology | Method for allowing evaluation of morbid state of bovine theileriasis |
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RU2698092C1 (en) * | 2018-04-10 | 2019-08-22 | Федеральное государственное бюджетное научное учреждение "Научно-исследовательский институт общей патологии и патофизиологии" | Method for determining predisposition to atherosclerosis disease based on determining expression of genes involved in accumulation of cholesterol |
JP2020508444A (en) * | 2017-02-20 | 2020-03-19 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | Serological assay for asymptomatic cerebral ischemia |
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- 2007-10-04 BR BRPI0717803-4A patent/BRPI0717803A2/en not_active IP Right Cessation
- 2007-10-04 US US12/311,542 patent/US20100196880A1/en not_active Abandoned
- 2007-10-04 MX MX2009003583A patent/MX2009003583A/en active IP Right Grant
- 2007-10-04 WO PCT/US2007/021451 patent/WO2008057160A2/en active Application Filing
- 2007-10-04 EP EP07867209A patent/EP2069524A4/en not_active Withdrawn
- 2007-10-04 CA CA002665164A patent/CA2665164A1/en not_active Abandoned
- 2007-10-04 RU RU2009116433/10A patent/RU2520080C2/en not_active IP Right Cessation
- 2007-10-04 JP JP2009531477A patent/JP2010505420A/en active Pending
-
2009
- 2009-05-05 ZA ZA200903094A patent/ZA200903094B/en unknown
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- 2011-11-15 US US13/296,751 patent/US20120122717A1/en not_active Abandoned
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JP2010075121A (en) * | 2008-09-26 | 2010-04-08 | National Institute Of Advanced Industrial Science & Technology | Method for allowing evaluation of morbid state of bovine theileriasis |
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Also Published As
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BRPI0717803A2 (en) | 2013-11-19 |
MX2009003583A (en) | 2009-04-15 |
CN101627129A (en) | 2010-01-13 |
RU2009116433A (en) | 2010-11-20 |
CA2665164A1 (en) | 2008-05-15 |
EP2069524A2 (en) | 2009-06-17 |
AU2007318208A1 (en) | 2008-05-15 |
US20100196880A1 (en) | 2010-08-05 |
US20120122717A1 (en) | 2012-05-17 |
JP2010505420A (en) | 2010-02-25 |
ZA200903094B (en) | 2010-07-28 |
WO2008057160A3 (en) | 2009-05-14 |
CN101627129B (en) | 2014-07-02 |
AU2007318208B2 (en) | 2013-10-24 |
RU2520080C2 (en) | 2014-06-20 |
EP2069524A4 (en) | 2010-02-24 |
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