Methods of Detecting Signatures of Disease or Conditions in Bodily Fluids

Abstract

Methods and compositions for diagnosing the presence of a cancer cell in an individual are provided. Methods and compositions for identifying a tumor-specific signature in an individual having cancer are also provided. Methods and compositions for diagnosing the presence of an infectious agent in an individual and/or for identifying an infectious agent-specific signature in an infected individual are provided. Methods and compositions for diagnosing the presence of a disease in an individual are also provided. Methods and compositions for identifying a disease-specific signature in an individual having the disease are also provided.

1 - 26 . (canceled) 
     
     
         27 . A method for diagnosing the presence of a cancer cell in an individual comprising the steps of:
 isolating a population of phagocytic cells from an individual;   separating 2n phagocytic cells from >2n phagocytic cells;   obtaining a first expression profile from the 2n phagocytic cells;   obtaining a second expression profile from the >2n phagocytic cells;   comparing the first and second expression profiles;   identifying differential expression of one or more markers specific to the first expression profile; and   relating the differential expression of the one or more markers specific to the first expression profile to the presence of a cancer cell in the individual.   
     
     
         28 . The method of  claim 27 , wherein the one or more markers are selected from the group consisting of DNA, RNA, protein, lipid, carbohydrate and combinations thereof. 
     
     
         29 . The method of  claim 27 , wherein the one or more markers are selected from the group consisting of DNA, RNA, microRNA and combinations thereof corresponding to two or more cancer genes, oncogenes, tumor suppressor genes or combinations thereof. 
     
     
         30 . The method of  claim 27 , wherein the one or more markers are proteins or polypeptides encoded by two or more cancer genes, oncogenes, tumor suppressor genes or any combination thereof. 
     
     
         31 . The method of  claim 27 , wherein the blood phagocytic cell is selected from the group consisting of a neutrophil, a macrophage, a monocyte, a dendritic cell, a foam cell and any combination thereof. 
     
     
         32 . The method of  claim 27 , wherein the blood phagocytic cell is isolated from whole blood, urine, stool, saliva, lymph or cerebrospinal fluid. 
     
     
         33 . The method of  claim 32 , wherein the blood phagocytic cell is isolated using antibodies. 
     
     
         34 . The method of  claim 32 , wherein the blood phagocytic cell is separated using one or methods selected from the group consisting of fluorescence activated cell sorting, filtration, gradient-based centrifugation, elution and microfluidics. 
     
     
         35 . The method of  claim 32 , wherein the blood phagocytic cell is separated using a ligand that binds to a molecular receptor expressed on the plasma membranes of WBC populations. 
     
     
         36 . A method for diagnosing the presence of an infectious agent in an individual comprising the steps of:
 obtaining a first expression profile from a blood phagocytic cell from an individual;   obtaining a second expression profile from a blood non-phagocytic cell from the individual;   comparing the first and second expression profiles;   identifying differential expression of one or more markers specific to the first expression profile; and   relating the differential expression of the one or more markers specific to the first expression profile to the presence of an infectious agent in the individual.   
     
     
         37 . The method of  claim 36 , wherein the one or more markers are selected form the group consisting of pathogen DNA, pathogen RNA, pathogen protein, pathogen polypeptide, pathogen lipid and combinations thereof. 
     
     
         38 . The method of  claim 36 , wherein the infectious agent is selected from the group consisting of a virus, a bacterium, a fungus, a parasite and an infectious protein. 
     
     
         39 . A method for identifying an infectious agent-specific signature in an infected individual comprising the steps of:
 obtaining a first expression profile from a blood phagocytic cell from an infected individual;   obtaining a second expression profile from a blood non-phagocytic cell from the infected individual;   comparing the first and second expression profiles;   identifying differential expression of two or more markers specific to the first expression profile; and   relating the differential expression of the two or more markers specific to an infectious agent-specific signature in the infected individual.   
     
     
         40 . The method of  claim 39 , wherein the two or more markers are selected form the group consisting of pathogen DNA, pathogen RNA, pathogen protein, pathogen polypeptide, pathogen lipid and combinations thereof. 
     
     
         41 . The method of  claim 39 , wherein the infectious agent is selected from the group consisting of a virus, a bacterium, a fungus, a parasite and an infectious protein. 
     
     
         42 . A method for diagnosing the presence of an infectious agent in an individual comprising the steps of:
 obtaining a first expression profile from a blood phagocytic cell from an individual;   obtaining a second expression profile from a blood non-phagocytic cell from the individual;   comparing the first and second expression profiles;   identifying the presence of a circulating tumor cell or subcellular fragment thereof specific to the first expression profile; and   relating the presence of a circulating tumor cell or subcellular fragment thereof to the presence of an infectious agent in the individual.   
     
     
         43 . A method for diagnosing the presence of an infectious agent in an individual comprising the steps of:
 isolating a population of phagocytic cells from an individual;   separating 2n phagocytic cells from >2n phagocytic cells;   obtaining a first expression profile from the 2n phagocytic cells;   obtaining a second expression profile from the >2n phagocytic cells;   comparing the first and second expression profiles;   identifying differential expression of one or more markers specific to the first expression profile; and   relating the differential expression of the one or more markers specific to the first expression profile to the presence of an infectious agent in the individual.   
     
     
         44 . The method of  claim 43 , wherein the one or more markers are selected form the group consisting of pathogen DNA, pathogen RNA, pathogen protein, pathogen polypeptide, pathogen lipid and combinations thereof. 
     
     
         45 . The method of  claim 43 , wherein the infectious agent is selected from the group consisting of a virus, a bacterium, a fungus, a parasite and an infectious protein. 
     
     
         46 . The method of  claim 43 , wherein the blood phagocytic cell is selected from the group consisting of a neutrophil, a macrophage, a monocyte, a dendritic cell, a foam cell and any combination thereof. 
     
     
         47 . The method of  claim 43 , wherein the blood phagocytic cell is isolated from whole blood, urine, stool, saliva, lymph or cerebrospinal fluid. 
     
     
         48 . The method of  claim 47 , wherein the blood phagocytic cell is isolated using antibodies. 
     
     
         49 . The method of  claim 47 , wherein the blood phagocytic cell is separated using one or methods selected from the group consisting of fluorescence activated cell sorting, filtration, gradient-based centrifugation, elution and microfluidics. 
     
     
         50 . The method of  claim 47 , wherein the blood phagocytic cell is separated using a ligand that binds to a molecular receptor expressed on the plasma membranes of WBC populations. 
     
     
         51 . One or more markers of a condition differentially expressed between phagocytic cells and nonphagocytic cells from a common source. 
     
     
         52 . One or more markers of a condition differentially expressed between phagocytic cells having a DNA content of 2n and phagocytic cells having a DNA content of greater than 2n from a common source. 
     
     
         53 . The one or more markers of  claim 51  being DNA, RNA, microRNA, protein, lipid, or carbohydrate or combinations thereof. 
     
     
         54 . The one or more markers of  claim 52  being DNA, RNA, microRNA, protein, lipid, or carbohydrate or combinations thereof. 
     
     
         55 . The one or more markers of  claim 51  wherein the phagocytic cells are neutrophils, macrophages, monocytes, dendritic cells or foam cells or combinations thereof. 
     
     
         56 . The one or more markers of  claim 52  wherein the phagocytic cells are neutrophils, macrophages, monocytes, dendritic cells or foam cells or combinations thereof. 
     
     
         57 . The one or more markers of  claim 51  wherein the nonphagocytic cells are T cells, B cells, null cells, or basophils or combinations thereof. 
     
     
         58 . Protein profile, DNA profile, RNA profile, metabolite profile, glycome profile, glycoprotein profile, carbohydrate profile, lipoprotein profile or lipid profile specific to blood phagocytic cells compared to blood nonphagocytic cells from a common source. 
     
     
         59 . Protein profile, DNA profile, RNA profile, metabolite profile, glycome profile, glycoprotein profile, carbohydrate profile, lipoprotein profile or lipid profile specific to blood phagocytic cells having a DNA content of greater than 2n compared to blood phagocytic cells having a DNA content of 2n from a common source. 
     
     
         60 . A kit for detecting the presence of one or more markers associated with cancer and/or an infectious agent in a biological sample, wherein the kit comprises a labeled compound or agent for detecting a marker polypeptide, protein lipid, oligosaccharide, mRNA, microRNA, or genomic DNA, and a standard such as a non-phagocytic cell or a 2n cell to compare the amount of marker in the sample with the standard.