Method for diagnosing and/or predicting of a septic syndrome

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

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C435S007100, C435S091200, C435S091510, C536S023500, C530S350000

Reexamination Certificate

active

07622249

ABSTRACT:
The present invention relates to a method for diagnosing and/or predicting a septic syndrome, wherein:a. a biological sample from the patient is made available and biological material is extracted from the biological sampleb. at least four specific reagents which are selected from the following specific reagents are made available: reagent which is specific for the target gene IL-10, reagent which is specific for the target gene TGFβ, reagent which is specific for the target gene HMG1, reagent which is specific for the target gene T-bet, reagent which is specific for the target gene IL-1β, reagent which is specific for the target gene TNFα and reagent which is specific for the target gene GATA-3c. the expression of at least four target genes selected from: IL-10, TGFβ, HMG1, T-bet, IL-1β, TNFα and GATA-3 is determined.The present invention also relates to a kit for diagnosing and/or predicting a septic syndrome.

REFERENCES:
patent: 4672040 (1987-06-01), Josephson
patent: 4683195 (1987-07-01), Mullis et al.
patent: 4683202 (1987-07-01), Mullis
patent: 4800159 (1989-01-01), Mullis et al.
patent: 4981783 (1991-01-01), Augenlicht
patent: 5234809 (1993-08-01), Boom et al.
patent: 5399491 (1995-03-01), Kacian et al.
patent: 5445934 (1995-08-01), Fodor et al.
patent: 5700637 (1997-12-01), Southern
patent: 5744305 (1998-04-01), Fodor et al.
patent: 5750338 (1998-05-01), Collins et al.
patent: 5807522 (1998-09-01), Brown et al.
patent: 6303321 (2001-10-01), Tracey et al.
patent: 2005/0037344 (2005-02-01), Stuhlmuller et al.
patent: 0 201 184 (1986-12-01), None
patent: 1 310 567 (2003-05-01), None
patent: 2 780 059 (1999-12-01), None
patent: WO 90/01069 (1990-02-01), None
patent: WO 90/06995 (1990-06-01), None
patent: WO 91/02818 (1991-03-01), None
patent: WO 91/19812 (1991-12-01), None
patent: WO 94/12670 (1994-06-01), None
patent: WO 95/08000 (1995-03-01), None
patent: WO 97/45202 (1997-12-01), None
patent: WO 99/15321 (1999-04-01), None
patent: WO 99/35500 (1999-07-01), None
patent: WO 99/53304 (1999-10-01), None
patent: WO 00/05338 (2000-02-01), None
patent: WO 2004/005539 (2004-01-01), None
Zanotti, S. et al. Cytokine modulation in sepsis and septic shock. Expert opinion on investigational drugs. 11(8):1061-1075 (Aug. 2002).
Hultgren, O.H. et al. Microbes and Infection 6:529-535 (Mar. 31, 2004).
Szabo, S.J. et al. Science 295:338-342 (Jan. 11, 2002).
Thijs et al., “Time course of cytokine levels in sepsis,” Intensive Care Med, 21: S258-S263, 1995.
Casey et al., “Plasma Cytokine and Endotoxin Lewis Correlate with Survival in Patients with the Sepsis Syndrome,” Ann Intern Medicine, vol. 119, Issue 8, pp. 771-778, 1993.
Van der Poll et al., “Antiinflammatory Cytokine Responses during Clinical Sepsis and Experimental Endotoxemia: Sequential Measurements of Plasma Soluble Interleukin (IL)-1 Receptor Type II, IL-10, and IL-13,” The Journal of Infectious Diseases, 1997, 175:118-122, 1997.
Wang et al, “HMG-1 as a Late Mediator of Endotoxin Lethality in Mice,” Science, vol. 285, pp. 248-251, 1999.
Boom et al., “Rapid and Simple Method for Purification of Nucleic Acids,” Journal of Clinical Microbiology, vol. 28, No. 3, pp. 495-503, 1990.
Levison et al., “New approaches to the isolation of DNA by ion-exchange chromatography,” Journal of Chromatography, 827, p. 337-344, 1998.
Kricka et al., “Nucleic Acid Detection Technologies—Labels, Strategies, and Formats,” Clinical Chemistry, No. 45:4, pp. 453-458, 1999.
Keller et al., DNA Probes, 2nd Ed., Stockton Press, sections 5 and 6, pp. 173-249, 1993.
Holland et al., “Detection of specific polymerase chain reaction product by utilizing the 5′→3′ exonuclease activity ofThermus aquaticusDNA polymerase,” Proc. Nat. Acad. Sci., vol. 88, pp. 7276-7280. 1991.
Chee et al., “Accessing Genetic Information with High-Density DNA arrays,” Science, vol. 274, No. 5287, pp. 610-614 1996.
Pease et al., “Light-generated oligonucleotide arrays for rapid DNA sequence analysis”, Proc. Natl. Acad. Sci. USA, vol. 91, pp. 5022-5026, 1994.
Ramsay, “DNA Chips: State-of-the art” Nature Biotechnology, vol. 16, pp. 40-44; 1998.
Cheng et al., “Microchip-based Devices for Molecular Diagnosis of Genetic Diseases,” Molecular Diagnosis, vol. 1, No. 3, pp. 183-200, 1996.
Livache et al., “Preparation of a DNA matrix via an electrochemically directed copolymerization of pyrrole and oligonucleotides bearing a pyrrole group,” Nucleic Acids Research, vol. 22 No. 15, pp. 2915-2921, 1994.
Cheng et al., “Preparation and hybridization analysis of DNA/RNA fromE. colion microfabricated bioelectronic chips,” Nature Biotechnology, vol. 16 pp. 541-546, 1998.
F. Ginot, “Oligonucleotide Micro-Arrays for Identification of Unknown Mutations: How Far From Reality?” Human Mutation, No. 10, pp. 1-10, 1997.
Bustin, “Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems,” Journal of Molecular Endocrinology, vol. 29, pp. 23-39, 2002.
Giulietti et al., “An Overview of Real-Time Quantitative PCR: Applications to Quantify Cytokine Gene Expression,” Methods, vol. 25, 2001, pp. 386-401.
Bone et al., “Definitions for Sepsis and Organ Failure and Guidelines for the Use of Innovative Therapies in Sepsis,” The ACCP/SCCM Consensus Conference Committee, American College of Chest Physicians/Society of Critical Care Medicine,Chest 101, vol. 6; 1992, pp. 1644-1655.
Stuhlmüller et al., “Identification of Known and Novel Genes in Activated Monocytes from Patients with Rheumatoid Arthritis,” Arthritis and Rheumatism, vol. 43, No. 4, Apr. 2000, pp. 775-790.
Berner et al., “Plasma Levels and Gene Expression of Granulocyte Colony-Stimulating Factor, Tumor Necrosis Factor-α, Interleukin (IL)-1β, IL-6, IL8, and Soluble Intercellular Adhesion Molecule-1 in Neonatal Early Onset Sepsis,” Pediatric Research, vol. 44, No. 4, 1998, pp. 469-477.
Lee, “Proteomics: a technology-driven and technology-limited discovery science,” Trends in Biotechnology, vol. 19, No. 6, Jun. 1, 2001, pp. 217-222.

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