Literature DB >> 20636007

Killer artificial antigen-presenting cells: the synthetic embodiment of a 'guided missile'.

Christian Schütz1, Mathias Oelke, Jonathan P Schneck, Andreas Mackensen, Martin Fleck.   

Abstract

At present, the treatment of T-cell-dependent autoimmune diseases relies exclusively on strategies leading to nonspecific suppression of the immune systems causing a substantial reduced ability to control concomitant infections or malignancies. Furthermore, long-term treatment with most drugs is accompanied by several serious adverse effects and does not consequently result in cure of the primary immunological malfunction. By contrast, antigen-specific immunotherapy offers the potential to achieve the highest therapeutic efficiency in accordance with minimal adverse effects. Therefore, several studies have been performed utilizing antigen-presenting cells specifically engineered to deplete allo- or antigen-specific T cells ('guided missiles'). Many of these strategies take advantage of the Fas/Fas ligand signaling pathway to efficiently induce antigen-presenting cell-mediated apoptosis in targeted T cells. In this article, we discuss the advantages and shortcomings of a novel non-cell-based 'killer artificial antigen-presenting cell' strategy, developed to overcome obstacles related to current cell-based approaches for the treatment of T-cell-mediated autoimmunity.

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Year:  2010        PMID: 20636007      PMCID: PMC2941805          DOI: 10.2217/imt.10.26

Source DB:  PubMed          Journal:  Immunotherapy        ISSN: 1750-743X            Impact factor:   4.196


  94 in total

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10.  Killer artificial antigen-presenting cells: a novel strategy to delete specific T cells.

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7.  A biodegradable killer microparticle to selectively deplete antigen-specific T cells in vitro and in vivo.

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9.  Interleukin-5 supports the expansion of fas ligand-expressing killer B cells that induce antigen-specific apoptosis of CD4(+) T cells and secrete interleukin-10.

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10.  Saporin-conjugated tetramers identify efficacious anti-HIV CD8+ T-cell specificities.

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