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  • 1
    ISSN: 1432-0851
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A trial of adoptive immunotherapy was performed in which long-term cultured, interleukin-2 (IL2)-dependent T-lymphocytes were administered to patients with metastatic adenocarcinoma of the lung. Lymphocytes were isolated from explants of cancer tissues that were cultured in medium with recombinant IL-2. These T-cells expressed surface markers of activation, and killed a broad panel of tumor targets. Intravenously injected 111indium-labeled T-cell blasts distributed primarily to lungs, liver, and spleen. Despite a paucity of infused lymphocytes detected by external imaging at sites of tumor, five of seven patients showed reduction of their cancers. However, in no case was greater than 50% reduction of total tumor burden achieved. Evidence of increased delayed cutaneous hypersensitivity to protein antigens was observed in three patients following therapy. We conclude that long-term cultured tumor-derived T-cells can be transferred safely into humans and that these cells may be capable of enhancing immune responses and mediating tumor reduction in vivo.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Springer seminars in immunopathology 10 (1988), S. 169-180 
    ISSN: 1432-2196
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Conclusions The observation that rheumatoid synovial-derived lymphocytes display clonal dominance may have important implications in the understanding of the underlying pathogenic processes in RA. Isolation of the relevant T cell clones will allow further characterization including the development of anti-clonotypic mAb which could be used for diagnostic and possibly even for therapeutic purposes. Functional analysis of the clones could be used as an approach to identify the antigen(s) that trigger the disease. Our observations, however, raise a number of points. First, the detection of clonal dominance in a T cell population within a tissue or in blood has been considered a marker of malignancy [9, 13]. Recent studies of several skin diseases suggest that T cell oligoclonality observed in some of these lesions represents a selected repertoire of responding T cells; our study shows that T cell clonality is not restricted to lymphoproliferative diseases but may indeed be a feature of certain inflammatory processes as well.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-2592
    Keywords: Monocyte development ; tetanus toxoid ; antigen presentation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The requirement for linked HLA-D antigen recognition for the proliferation of antigen-specific T-cell blasts provides a method for testing antigen presentation of human monocytes. We used maternal tetanus toxoid-specific T-cell blasts to show that human newborn monocytes can process and present antigen at least as well as maternal monocytes. These results suggest that human monocytes are relatively more mature at birth than those of newborn rats and mice. A major role for monocyte-macrophage immaturity in limiting the immune responses of human newborns is therefore unlikely.
    Type of Medium: Electronic Resource
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