摘要:
The present invention relates in a first aspect to a method for diagnosing tuberculosis infection calculating a score based on the expression of a predetermined set of genes and as well as diagnosing or predicting the clinical outcome of the tuberculosis infection based on said score. In another aspect, a method for treatment monitoring and determining treatment duration in an individual with tuberculosis infection is provided. Said method includes the determination of the expression level of predetermined genes, calculating a value based thereon and the therapy monitoring or treatment monitoring and determining treatment duration in said individual accordingly. Moreover a method for determining the therapy-end of a treatment of tuberculosis infection in an individual affected with tuberculosis infection is provided. Said method includes the consideration of the expression level of predetermined genes together with the scores and values identified and calculating whether therapy is completed or not based on the value, the score and the expression level of said predetermined genes accordingly. In a further aspect, the use of a test kit or the use of kits of parts for conducting the methods according to the present invention is provided. Further, an array comprising means for detecting the expression of predetermined genes is identified as well as the use of the same. Moreover, a computer implemented method is provided as well as a computer readable medium or computer program product having computer executable instructions for performing the steps of the method disclosed herein.
摘要:
The present invention relates to a pharmaceutical composition comprising or consisting of a combination of (a) two or more peptides, each peptide consisting of or comprising 17 to 23 amino acids, wherein the amino acids in positions 1 to 23, counted from the N-terminus, are as follows (1) G, S or lacking; (2) C or lacking; (3) K or R; (4) K or R; (5) Y, W or F; (6) K or R; (7) K or R; (8) F, W or L; (9) K or R; (10) K or L or lacking; (11) W, L or F; (12) K or R; (13) F, Y or C; (14) K or R; (15) G or Q; (16) K or R; (17) F, L or W; (18) F or W; (19) F, L or W; (20) W or F; (21) C or lacking; (22) F or G or lacking; (23) G or lacking; or (b) one or more peptides, each peptide consisting of or comprising 17 to 23 amino acids, wherein the amino acids in positions 1 to 23, counted from the N-terminus, are as follows (1) G, S or lacking; (2) C or lacking; (3) K or R; (4) K or R; (5) Y, W or F; (6) K or R; (7) K or R; (8) F, W or L; (9) K or R; (10) K or L or lacking; (11 ) W, L or F; (12) K or R; (13) F, Y or C; (14) K or R; (15) G or Q; (16) K or R; (17) F, L or W; (18) F or W; (19) F, L or W; (20) W or F; (21) C or lacking; (22) F or G or lacking; (23) G or lacking, and one or more antibiotics selected from small organic molecule antibiotics such as ceftriaxone, oxacillin, amoxicillin, amikacin, ciprofloxacin, erythromycin, imipenem and tetracycline, and peptidic antibiotics such as daptomycin and vancomycin.
摘要:
The present invention relates to L-arabino-oligosaccharides, in particular synthetically produced L-arabino-oligosaccharides and their uses for the prophylaxis of allergic reactions in mammals.
摘要:
The present invention relates to kits comprising 2,4-dichlorophenoxyacetate derivatives as well as antibodies that bind to these derivatives. Inter alia, the kits can be used to label biomolecules for analytical and diagnostic applications. Some of the compounds described here can be used to label biomolecules under physiological conditions and without having to apply in situ activation. Furthermore, the presence of spacers within the 2,4-dichlorophenoxyacetate derivatives improves their binding to antibodies.
摘要:
The invention relates to oligoribo- and oligodesoxyribonucleotides which are suitable for treating pathological conditions that are accompanied by increased cell proliferation. Said oligoribo- and oligodesoxyribonucleotides are characterised in that they are able to hybridise with the mRNA which codes the protein Ki-67, this protein being associated with the cell cycle.
摘要:
Die Erfindung betrifft Erzeugnisse, die einen Hemmer cyclinabhängiger Proteinkinasen und einen oder mehrere Modulatoren mindestens eines weiteren proteinmodifizierenden Enzyms als Kombinationspräparat zur gleichzeitigen, getrennten oder zeitlich abgestuften Anwendung als Arzneimittel enthalten. Die Erzeugnisse eignen sich insbesondere zu Anwendung in der Tumortherapie.