نتایج جستجو برای: cd52

تعداد نتایج: 350  

2010
Carmen Diana Schweighofer Clemens-Martin Wendtner

The CD52-targeting antibody alemtuzumab is established in clinical practice with convincing activity in relapsed and refractory chronic lymphocytic leukemia (CLL), particularly in patients with high-risk features and adverse prognosis. In the CAM307 study alemtuzumab was tested and finally approved as a first-line single agent, even though the hurdle with chlorambucil as the contender was not s...

2018
Peter E. van Bommel Yuan He Ilona Schepel Mark A. J. M. Hendriks Valerie R. Wiersma Robert J. van Ginkel Tom van Meerten Emanuele Ammatuna Gerwin Huls Douwe F. Samplonius Wijnand Helfrich Edwin Bremer

Here, we report on a novel bispecific antibody-derivative, designated RTX-CD47, with unique capacity for CD20-directed inhibition of CD47-SIRPα "don't eat me" signaling. RTX-CD47 comprises a CD20-targeting scFv antibody fragment derived from rituximab fused in tandem to a CD47-blocking scFv. Single agent treatment with RTX-CD47 triggered significant phagocytic removal of CD20pos/CD47pos maligna...

Journal: :Haematologica 2005
Wendy Louise Osborne Anne L Lennard

Alemtuzumab (Campath 1H) is a recombinant DNA derived humanized monoclonal antibody which targets CD52 antigens on B and T cells. It is increasingly used as a conditioning agent for bone marrow transplantation. We describe the case of a 37 year old woman who developed acute renal failure and disseminated intravascular coagulation (DIC) following one dose of Campath and Fludarabine. Campath was ...

2015
Hans-Peter Hartung Orhan Aktas Alexey N Boyko

Alemtuzumab is a humanized monoclonal antibody directed against CD52 to deplete circulating T and B lymphocytes; lymphocyte depletion is followed by a distinctive pattern of T- and B-cell repopulation, changing the balance of the immune system. This review reports the efficacy and safety findings of the phase 2 CAMMS223 trial and the phase 3 CARE-MS I and II trials investigating alemtuzumab for...

2016
Fahd A. Al-Khamis

This review discusses the mechanisms of action of 4 immune modulating drugs currently used in the treatment of multiple sclerosis (MS), including Alemtuzumab, a humanized monoclonal antibody that functions by targeting CD52, an antigen primarily expressed on T and B lymphocytes and monocytes/macrophages, resulting in their depletion and subsequent repopulation; Dimethyl fumarate that switches c...

2015
Rachel Babij Jai S Perumal

Alemtuzumab is the newest disease-modifying therapy approved for the treatment of relapsing multiple sclerosis. Alemtuzumab is an anti-CD52 targeted antibody that causes lysis of T and B lymphocytes, monocytes, natural killer cells, macrophages, and dendritic cells. Following its administration, a prolonged T-cell lymphopenia results with emergence of a reconstituted immune system that differs ...

2016
Mark D. Willis Neil P. Robertson

Alemtuzumab is a humanised anti-CD52 monoclonal antibody approved for use in active, relapsing multiple sclerosis (MS). Administration results in a rapid depletion of circulating lymphocytes with a subsequent beneficial immune reconstitution. Early open-label experience and recent clinical trials have demonstrated a dramatic effect on relapse rates as well as a positive effect on radiological d...

Journal: :Haematologica 2003
Laura Marbello Annamaria Nosari Gianpaolo Carrafiello Michela Anghilieri Clara Cesana Anna Maria Cafro Giovanna D'Avanzo Enrica Morra

Invasive aspergillosis in hematologic patients is an opportunistic infection difficult to treat. The infection localisation in the central nervous system has a high mortality rate. We describe a patient with advanced chronic lymphocytic leukaemia with a high grade of immunodepression, who developed pulmonary and cerebral aspergillosis resistant to amphotericin B deoxycolate during treatment wit...

2017
Roman Volchenkov Vegard Nygaard Zeynep Sener Bjørn Steen Skålhegg

The IL-17-producing CD4+ T helper cell (Th17) differentiation is affected by stimulation of the aryl hydrocarbon receptor (AhR) pathway and by hypoxia-inducible factor 1 alpha (HIF-1α). In some cases, Th17 become non-pathogenic and produce IL-10. However, the initiating events triggering this phenotype are yet to be fully understood. Here, we show that such cells may be differentiated at low ox...

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