antibody dependent cellular cytotoxicity oor Spaans
antibody dependent cellular cytotoxicity
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ADCC
citotoxicidad celular dependiente de anticuerpos
citotoxicidad mediada por células dependientes de anticuerpos
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Antibody-dependent cellular cytotoxicity is less well understood than either of the previous two mechanisms.
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Other mechanisms however, such as antibody-dependent cellular cytotoxicity and/or phagocytosis, may be possible.
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Possible anti-tumor mechanisms include complement activation and antibody-dependent cellular cytotoxicity utilizing natural killer cells or monocytes as effector cells.
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However the former is of the IgG1 type, the latter of the IgG2 type; consequences on antibody-dependent cellular cytotoxicity can be quite different.
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Possible mechanisms of effector-mediated cell lysis include complement-dependent cytotoxicity (CDC) resulting from C#q binding, and antibody-dependent cellular cytotoxicity (ADCC) mediated by one or more of the Fc receptors on the surface of granulocytes, macrophages and NK cells
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To evaluate the immune status of patients, various immune parameters such as 1-chloro-2, 4-dinitrobenzene (DNCB) test, T-lymphocyte count, PHA- and concanavalin-A-stimulated lymphoblastogenesis, and antibody-dependent cellular cytotoxicity (ADCC) activity were checked before surgery and 3–4 months postoperatively.
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Herceptin® may induce antibody dependent cellular cytotoxicity (ADCC).
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This process, called antibody-dependent cellular cytotoxicity, can cause inflammation of surrounding tissues and damage to healthy cells.
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Also called antibody-dependent cell-mediated cytotoxicity and antibody-dependent cellular cytotoxicity.
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Also called ADCC and antibody-dependent cellular cytotoxicity.
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· Nimotuzumab-mediated antibody-dependent cellular cytotoxicity activity on target tumor cell lines depends on the expression level of the epidermal growth factor receptor
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The homodimeric antibody thus generated may have improved internalization capability and/or increased complement-mediated cell killing and antibody-dependent cellular cytotoxicity (ADCC).
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Secondly, antibodies can recruit immune cells to the target tissue by their Fc domain, to initiate antibody-dependent cellular cytotoxicity (ADCC) or complement-dependent cytotoxicity (CDC).
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After the interaccion of these receptors with antibodies a wide range of biological responses begin, that include phagocytosis, antibody dependent cellular cytotoxicity and relase of inflammatory mediators.
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The cell can also be destroyed by a process called antibody-dependent cellular cytotoxicity, in which the pathogen does not need to be phagocytosed to be destroyed.
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IgGa and IgGb isotypes are effective in both complement fixation and antibody-dependant cellular cytotoxicity assays in vitro [32, 33], but their effector function in vivo has not been determined.
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Monoclonal antibodies of the IgG1 isotype may activate the complement pathway and mediate their effects via antibody-dependent cellular cytotoxicity (ADCC) that we discussed in the introduction to antibody therapies.
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The homodimeric antibody thus generated may have improved internalization capability and/or increased complement-mediated cell killing and antibody-dependent cellular cytotoxicity (ADCC). See Caron et al. J. Exp Med.
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This recognition by CD16 (low-affinity receptor for the Fc portion of IgG1 and IgG3) results in the destruction of the infected cell through a mechanism known as antibody-dependent cellular cytotoxicity (ADCC).
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The T-cell response to tumors is modulated by other cells of the immune system; some cells require the presence of humoral antibodies directed against the tumor cells (antibody-dependent cellular cytotoxicity) to initiate the interactions that lead to the death of tumor cells.
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To establish if HLA-E could be a factor that renders colorectal cancer cells less susceptible to antibody-dependent cellular cytotoxicity (ADCC), in the present study we analysed Cetuximab-mediated cytotoxicity against several colorectal cancer cell lines expressing, or not, HLA-E at the cell surface.
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Conjugates of antibodies of the invention can also be used to reduce tissue factor levels in a mammal, particularly a human, by administering to the mammal an effective amount of an antibody of the invention that is covalently attached to a cellular toxin or an effector molecule to provide the ability of complement fixation and cytotoxicity mediated antibody-dependent cell, whereby the antibody conjugate contacts cells expressing tissue factor to thereby reduce tissue factor levels in the diagnóstico in vivo de TF humano nativo.
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