Abstract: There is provided a method for detecting sleep disordered breathing (SDB-) events. The method comprises receiving an arousal signal representative of an occurrence of an autonomic arousal; receiving an SDB-signal representative of an occurrence of an SDB-event; and generating a confirmation signal representing confirming that the SDB-signal is representative of the occurrence of the SDB-event based on the arousal signal. Further there is provided a detecting device for detecting SDB-events. The detecting device comprises a sensor system; and a processing unit connected to the sensor system. The sensor system is configured to generate an arousal signal and is configured to generate an SDB-signal. The arousal signal is representative of an occurrence of an autonomic arousal. The SDB-signal is representative of an occurrence of an SDB-event. The processing unit is configured to perform the method for detecting sleep disordered breathing events.

Abstract: A method for synchronizing recordings of two wearable devices (12,14) worn by a user (16) in a specific use case is designed to measure a characteristic behaviour of the user over a period of time. The method comprises acquiring first recordings via a first wearable device (12) operable via a first clock, and acquiring concurrent second recordings via a second wearable device (14) operable via a second clock, wherein each clock has a clock drift and offset. The first and second wearable devices are synced with a hub executable app (18) executed on a hub device (20). A clock-time correction (62) is implemented via the hub executable app before processing (64) the respective recordings for the specific use case. The clock-time correction ensures that respective recordings have been corrected in time so that a difference between clocks, or clock drift, of the two wearable devices is no more than a threshold duration of a shortest event specific to the characteristic behaviour being measured.

Abstract: The present invention is directed to a molecule comprising a polypeptide having substantial homology with a CTL epitope selected from the group consisting of ADLMGYIPLV (Core131-140; SEQ ID NO:1), LLALLSCLTV (Core178-187; SEQ ID NO:2), QLRRHIDLLV (SEQ ID NO:55), LLCPAGHAV (NS31169-1177; SEQ ID NO:26), KLVALGINAV (NS31406-1415; SEQ ID NO:28), SLMAFTAAV (NS41789-1797; SEQ ID NO:34), LLFNILGGWV (NS41807-1816; SEQ ID NO:35), and ILDSFDPLV (NS52252-2260; SEQ ID NO:42). Such molecules are used for the treatment and prevention of acute or chronic HCV hepatitis; suitable pharmaceutical compositions and methods using such compositions are disclosed.

Abstract: The present invention is directed to a molecule comprising a polypeptide having substantial homology with a CTL epitope selected from the group consisting of ADLMGYIPLV (Core131-140; SEQ ID NO:1), LLALLSCLTV (Core178-187; SEQ ID NO:2), QLRRHIDLLV (SEQ ID NO:55), LLCPAGHAV (NS31169-1177; SEQ ID NO:26), KLVALGINAV (NS31406-1415; SEQ ID NO:28), SLMAFTAAV (NS41789-1797; SEQ ID NO:34), LLFNILGGWV (NS41807-1816; SEQ ID NO:35), and ILDSFDPLV (NS52252-2260; SEQ ID NO:42). Such molecules are used for the treatment and prevention of acute or chronic HCV hepatitis; suitable pharmaceutical compositions and methods using such compositions are disclosed.

Abstract: The hepatitis C virus (HCV) is the major cause of non-A, non-B vital hepatitis. The most striking feature of HCV induced liver disease is its tendency toward chronicity and slowly progressive liver cell injury. HLA Class I-restricted cytotoxic T lymphocyte (CTL) responses are considered to be a sine qua non for the effective clearance of vital infections. However, the characteristics of HCV-specific cytotoxic effector cells and identification of their cognate target antigens remains to be elucidated. This invention discloses novel HCV-derived peptides that are recognized by patient CTL. Peripheral blood mononuclear cells (PBMC) were obtained from HLA-A2 positive patients with chronic HCV infection and stimulated with HCV-derived peptides. Effector cells were tested for their ability to lyse HLA-A2-matched target cells sensitized either with a peptide or a vaccinia virus construct containing HCV sequences. Immunogenic HCV CTL peptides were identified in the putative core protein and nonstructural proteins (e.