Search Results - "FRENCH, Ruth R"

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    Mechanisms of killing by anti-CD20 monoclonal antibodies by Glennie, Martin J., French, Ruth R., Cragg, Mark S., Taylor, Ronald P.

    Published in Molecular immunology (01-09-2007)
    “…CD20 is a cell-surface marker expressed on mature B cells and most malignant B cells, but not stem or plasma cells. It is an ideal target for monoclonal…”
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    Anti-CD20 monoclonal antibodies: historical and future perspectives by LIM, Sean H, BEERS, Stephen A, FRENCH, Ruth R, JOHNSON, Peter W. M, GLENNIE, Martin J, CRAGG, Mark S

    Published in Haematologica (Roma) (01-01-2010)
    “…Antibodies to CD20 have confirmed the hypothesis that monoclonal reagents can be given in vivo to alleviate human diseases. The targeting of CD20 on normal,…”
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    CD20 as a Target for Therapeutic Type I and II Monoclonal Antibodies by Beers, Stephen A, Chan, Claude H.T, French, Ruth R, Cragg, Mark S, Glennie, Martin J

    Published in Seminars in hematology (01-04-2010)
    “…The last decade has seen the monoclonal antibody (mAb), rituximab, transform clinical management of many non-Hodgkin lymphomas and more recently provide new…”
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    Induction of Cytosolic Calcium Flux by CD20 Is Dependent upon B Cell Antigen Receptor Signaling by Walshe, Claire A., Beers, Stephen A., French, Ruth R., Chan, Claude H.T., Johnson, Peter W., Packham, Graham K., Glennie, Martin J., Cragg, Mark S.

    Published in The Journal of biological chemistry (20-06-2008)
    “…The anti-CD20 monoclonal antibody (mAb) rituximab is now routinely used for the treatment of non-Hodgkins lymphoma and is being examined in a wide range of…”
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    CD11c provides an effective immunotarget for the generation of both CD4 and CD8 T cell responses by Castro, Fernanda V.V, Tutt, Alison L, White, Ann L, Teeling, Jessica L, James, Sonya, French, Ruth R, Glennie, Martin J

    Published in European journal of immunology (01-08-2008)
    “…The magnitude and quality of T cell responses generated when Ag is targeted to receptors on DC is influenced by both the specific receptor targeted and its…”
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    On-target IgG hexamerisation driven by a C-terminal IgM tail-piece fusion variant confers augmented complement activation by Sopp, Joshua M., Peters, Shirley J., Rowley, Tania F., Oldham, Robert J., James, Sonya, Mockridge, Ian, French, Ruth R., Turner, Alison, Beers, Stephen A., Humphreys, David P., Cragg, Mark S.

    Published in Communications biology (02-09-2021)
    “…The majority of depleting monoclonal antibody (mAb) drugs elicit responses via Fc-FcγR and Fc-C1q interactions. Optimal C1q interaction is achieved through…”
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    Interaction with FcγRIIB is critical for the agonistic activity of anti-CD40 monoclonal antibody by White, Ann L, Chan, H T Claude, Roghanian, Ali, French, Ruth R, Mockridge, C Ian, Tutt, Alison L, Dixon, Sandra V, Ajona, Daniel, Verbeek, J Sjef, Al-Shamkhani, Aymen, Cragg, Mark S, Beers, Stephen A, Glennie, Martin J

    Published in The Journal of immunology (1950) (15-08-2011)
    “…A high activatory/inhibitory FcγR binding ratio is critical for the activity of mAb such as rituximab and alemtuzumab that attack cancer cells directly and…”
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    Antigenic modulation limits the effector cell mechanisms employed by type I anti-CD20 monoclonal antibodies by Tipton, Thomas R.W., Roghanian, Ali, Oldham, Robert J., Carter, Matthew J., Cox, Kerry L., Mockridge, C. Ian, French, Ruth R., Dahal, Lekh N., Duriez, Patrick J., Hargreaves, Philip G., Cragg, Mark S., Beers, Stephen A.

    Published in Blood (19-03-2015)
    “…Following the success of rituximab, 2 other anti-CD20 monoclonal antibodies (mAbs), ofatumumab and obinutuzumab, have entered clinical use. Ofatumumab has…”
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    Type II (tositumomab) anti-CD20 monoclonal antibody out performs type I (rituximab-like) reagents in B-cell depletion regardless of complement activation by Beers, Stephen A., Chan, Claude H.T., James, Sonya, French, Ruth R., Attfield, Kathrine E., Brennan, Claire M., Ahuja, Anupama, Shlomchik, Mark J., Cragg, Mark S., Glennie, Martin J.

    Published in Blood (15-11-2008)
    “…Anti-CD20 monoclonal antibodies (mAbs) are classified into type I (rituximab-like) or type II (tositumomab-like) based on their ability to redistribute CD20…”
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    Augmentation of CD134 (OX40)-dependent NK anti-tumour activity is dependent on antibody cross-linking by Turaj, Anna H., Cox, Kerry L., Penfold, Christine A., French, Ruth R., Mockridge, C. Ian, Willoughby, Jane E., Tutt, Alison L., Griffiths, Jordana, Johnson, Peter W. M., Glennie, Martin J., Levy, Ronald, Cragg, Mark S., Lim, Sean H.

    Published in Scientific reports (02-02-2018)
    “…CD134 (OX40) is a member of the tumour necrosis factor receptor superfamily (TNFRSF). It acts as a costimulatory receptor on T cells, but its role on NK cells…”
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    A new anti-idiotype antibody capable of binding rituximab on the surface of lymphoma cells by Cragg, Mark S., Bayne, Mike B., Tutt, Alison L., French, Ruth R., Beers, Stephen, Glennie, Martin J., Illidge, Timothy M.

    Published in Blood (15-10-2004)
    “…The chimeric anti-CD20 monoclonal antibody (mAb), rituximab, is an established part of the management of many non-Hodgkin lymphomas. The in vivo action of…”
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