نتایج جستجو برای: anti cd20

تعداد نتایج: 365619  

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2009
Tove Olafsen David Betting Vania E Kenanova Felix B Salazar Pat Clarke Jonathan Said Andrew A Raubitschek John M Timmerman Anna M Wu

UNLABELLED The CD20 cell surface antigen is expressed at high levels by over 90% of B-cell non-Hodgkin lymphomas (NHL) and is the target of the anti-CD20 monoclonal antibody rituximab. To provide more sensitive, tumor-specific PET imaging of NHL, we sought to develop PET agents targeting CD20. METHODS Two recombinant anti-CD20 rituximab fragments, a minibody (scFv-C(H)3 dimer; 80 kDa) and a m...

Journal: :PLoS Medicine 2008
Magdalena Winiarska Jacek Bil Ewa Wilczek Grzegorz M Wilczynski Malgorzata Lekka Patrick J Engelberts Wendy J. M Mackus Elzbieta Gorska Lukasz Bojarski Tomasz Stoklosa Dominika Nowis Zuzanna Kurzaj Marcin Makowski Eliza Glodkowska Tadeusz Issat Piotr Mrowka Witold Lasek Anna Dabrowska-Iwanicka Grzegorz W Basak Maria Wasik Krzysztof Warzocha Maciej Sinski Zbigniew Gaciong Marek Jakobisiak Paul W. H. I Parren Jakub Golab

BACKGROUND Rituximab is used in the treatment of CD20+ B cell lymphomas and other B cell lymphoproliferative disorders. Its clinical efficacy might be further improved by combinations with other drugs such as statins that inhibit cholesterol synthesis and show promising antilymphoma effects. The objective of this study was to evaluate the influence of statins on rituximab-induced killing of B c...

2017
Michael J. E. Marshall Richard J. Stopforth Mark S. Cragg

Therapeutic monoclonal antibodies (mAbs) have become one of the fastest growing classes of drugs in recent years and are approved for the treatment of a wide range of indications, from cancer to autoimmune disease. Perhaps the best studied target is the pan B-cell marker CD20. Indeed, the first mAb to receive approval by the Food and Drug Administration for use in cancer treatment was the CD20-...

2017
Letizia Polito Daniele Mercatelli Massimo Bortolotti Stefania Maiello Alice Djemil Maria Giulia Battelli Andrea Bolognesi

Immunotoxins (ITs) are hybrid proteins combining the binding specificity of antibodies with the cytocidal properties of toxins. They represent a promising approach to lymphoma therapy. The cytotoxicity of two immunotoxins obtained by chemical conjugation of the plant toxin saporin-S6 with the anti-CD20 chimeric antibody rituximab and the anti-CD22 murine antibody OM124 were evaluated on the CD2...

Journal: :Cancer research 1989
O W Press A G Farr K I Borroz S K Anderson P J Martin

Seven murine monoclonal antibodies (MoAbs) recognizing differentiation antigens present on B-lymphocytes were analyzed in preclinical studies for their potential use for antibody-targeted therapy of B-cell malignancies. MoAbs HD37 (anti-CD19), 1F5 (anti-CD20), HD6 (anti-CD22), MB-1 (anti-CD37), G28-5 (anti-CDw40), 7.2 (anti-class II), and DA4-4 (anti-IgM) were studied for their binding aviditie...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2013
Haifeng Zhang Liping Song Hongtu Ye Lide Hu Wenlu Liang Datao Liu

BACKGROUND Rituximab, a mouse Fab and human Fc chimeric antibody, has been widely used to treat Non-Hodgkin's lymphoma (NHL). However, only 48% of patients respond to the treatment and complete response rate is below 10%. Also, immunogenicity was reported in 17-20% patients receiving the treatment, making it unsuitable for long term diseases such as autoimmune disorders. It has been a hot resea...

Journal: :Blood 2011
Sean H Lim Andrew T Vaughan Margaret Ashton-Key Emily L Williams Sandra V Dixon H T Claude Chan Stephen A Beers Ruth R French Kerry L Cox Andrew J Davies Kathleen N Potter C Ian Mockridge David G Oscier Peter W M Johnson Mark S Cragg Martin J Glennie

The anti-CD20 mAb rituximab is central to the treatment of B-cell malignancies, but resistance remains a significant problem. We recently reported that resistance could be explained, in part, by internalization of rituximab (type I anti-CD20) from the surface of certain B-cell malignancies, thus limiting engagement of natural effectors and increasing mAb consumption. Internalization of rituxima...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2001
D Shan A K Gopal O W Press

Retinoids have been shown to be clinically useful in the biological therapy of certain myeloid and T-cell malignancies, whereas CD20 has proven to be an effective target in B-cell lymphoma immunotherapy. Both retinoic acid derivatives and anti-CD20 monoclonal antibodies have also been shown to induce apoptosis of malignant cells in vitro. Retinoid-induced apoptosis is thought to be mediated by ...

Journal: :Haematologica 2009
Marieke Griffioen Esther H M van Egmond Michel G D Kester Roel Willemze J H Frederik Falkenburg Mirjam H M Heemskerk

The aim of adoptive T-cell therapy of cancer is to selectively confer immunity against tumor cells. Autoimmune side effects, however, remain a risk, emphasizing the relevance of a suicide mechanism allowing in vivo elimination of infused T cells. We investigated the use of human CD20 as suicide gene in T-lymphocytes. Potential effects of forced CD20 expression on T-cell function were investigat...

Journal: :Journal of immunology 2004
Adam D Kennedy Paul V Beum Michael D Solga David J DiLillo Margaret A Lindorfer Charles E Hess John J Densmore Michael E Williams Ronald P Taylor

Complement plays an important role in the immunotherapeutic action of the anti-CD20 mAb rituximab, and therefore we investigated whether complement might be the limiting factor in rituximab therapy. Our in vitro studies indicate that at high cell densities, binding of rituximab to human CD20(+) cells leads to loss of complement activity and consumption of component C2. Infusion of rituximab in ...

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