摘要:
The invention relates to novel peptides and partial peptide sequences for the diagnosis and treatment of inflammation and sepsis, said peptides and partial peptide sequences being formed during the inflammation and/or infection of primates and humans, and the use of the same or the use of antibodies formed against said peptides for diagnosis and treatment.
摘要:
Verwendungen der Glycin-N-Acyl-Transferase (GNAT) aus Körperflüssigkeiten oder Körpergeweben in der Human- und Tiermedizin als Markerpeptid zum diagnostischen Nachweis, für die Verlaufsprognose und für die Verlaufskontrolle von Entzündungen und Infektionen und/oder als Target für die therapeutische Beeinflussung des Verlaufs von Entzündungen und/oder Infektionen.
摘要:
Verfahren zur differentialdiagnostischen Früherkennung und Erkennung, für die Verlaufsprognose und die Beurteilung des Schweregrads und zur therapiebegleitenden Verlaufsbeurteilung von Sepsis und sepsisähnlichen systemischen Infektionen, bei dem man, vorzugsweise unter Bestimmung mindestens eines weiteren für die Sepsisdiagnose geeigneten Parameters, die Menge von S100B in einer biologischen Flüssigkeit eines Patienten, bei dem eine Sepsis vorliegt oder ein Verdacht auf Sepsis besteht, bestimmt und aus der bestimmten Menge an S100B Schlüsse hinsichtlich des Vorliegens, des zu erwartenden Verlaufs, des Schweregrads und/oder des Erfolgs eingeleiteter Maßnahmen zur Therapie der Sepsis zieht.
摘要:
The invention relates to a method for detecting thyroid autoantibodies in a biological sample taken from a patient in the context of differential diagnosis of diseases associated with changes in and/or malfunctions of the thyroid. The process of detecting the presence and/or quantity of thyroid autoantibodies in the sample uses an immunodiagnostic method of detection whereby a measurement signal is provided per detection. Said measurement signal generally represents the presence and quantity of at least two antibodies, including anti-TPO-autoantibodies and anti-Tg-autoantibodies, in the sample. Said method increases the selectivity and sensitivity of the detection of autoantibodies typical for certain autoimmune diseases whilst simplifying the process.
摘要:
Immunoassay for procalcitonin in a biological sample from a patient comprises selectively determining full-length procalcitonin 1-116 with alanine and proline at positions 1 and 2. An independent claim is also included for an antibody that selectively binds to procalcitonin 1-116.
摘要翻译:用于确定患者生物样品中降钙素原和降钙素原衍生物用于诊断目的的免疫诊断方法,特别是用于监测和控制局部或全身细菌感染,炎症,败血症或神经退行性疾病的治疗和监测进程 ,其中在完整降钙素原1-116(SEQ ID NO:1)的氨基末端的1和2位具有氨基酸丙氨酸和脯氨酸(Ala-Pro,AP)的那些分子形式的降钙素原或降钙素原部分肽 NO:1)被选择性地确定,并且用于实施这种方法的抗体和试剂盒。
摘要:
In vitro method for the identification and early identification and for the concomitant monitoring of the therapy and cure of in particular drug-induced or addictive substance-induced liver damage, in which the occurrence of the human enzyme carbamoyl synthase 1 (CPS 1) or its concentration is determined in serum or plasma samples from patients who are being or have been treated with potentially liver-damaging drugs, or from people who take harmful stimulants and addictive substances or are exposed to hepatotoxic substances.
摘要:
The invention relates to the use of novel soluble cytokeratine-1 fragments from body fluids or tissues a marker peptides for the diagnostic detection of the course prognosis and course control of inflammations and infections and/or as a target for therapeutically influencing the course of inflammations and/or infections.
摘要:
The invention relates to a method for the early detection and detection, the progression prognosis and the evaluation of the degree of severity, and the treatment-accompanying progression evaluation of sepsis and sepsis-like systemic infections, and for the estimation of the danger which would be presented to patients at high risk of sepsis, by the development of a sepsis. According to the inventive method, the presence and/or quantity of anti-asialo-GM1 antibodies (anti-AGM1 antibodies), and antibodies which cross-react with the same, in a biological liquid of a patient or a patient at high risk of sepsis is determined, and conclusions are drawn from the presence and/or quantity of the same in terms of presence, expected progression, degree of severity or the success of a treatment for the inflammatory disease or sepsis, or in terms of the danger presented to a patient at high risk of sepsis. The inventive method enables potentially harmful banked blood to be eliminated if donor blood is used.