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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science, Ltd
    Clinical & experimental allergy 32 (2002), S. 0 
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1398-9995
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background: We report on a 37-year-old man without history of previous allergic disease who developed an aseptic intolerance reaction to a chromium-cobalt alloy, with local discomfort, loosening, and absence of fracture healing. Both in vivo and in vitro allergoimmunologic diagnostic tests were performed. Methods: Patch testing was done with a European standard series. Specific serum IgE was measured by CAP-FEIA. In addition to immunohistology (APAAP method), peri-implantar tissue was further analyzed by PCR to determine T-cell-receptor-γ rearrangement and thus the potential clonal (antigen-driven) T-cell repertoire. The actual tissue mRNA expression for IL-4, IL-6, and IFN-γ was visualized by RT-PCR. Results: Skin testing gave a delayed-type reaction to dichromate. Specific serum IgE to natural rubber latex and grass pollen was found – but without clinical symptoms. Immunohistology revealed a monocytic and dense T-cell infiltrate. The latter, instead of being random, showed an oligoclonal T-cell receptor rearrangement. In addition, there was TH1-type mediator expression (IL-6 and IFN-γ, but not IL-4). Conclusions: Skin test, examination of peri-implantar tissue, and the prompt healing after replacement of the osteosynthesis material suggest an allergic reaction. PCR analysis of peri-implantar tissue can further help to identify and understand allergy-mediated implant intolerance reactions.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1398-9995
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background: The peripheral blood mononuclear cells (PBMC) of individuals with nickel contact allergy are reported to proliferate to a varying degree upon nickel stimulation in vitro. Different phenotypes of the T cells involved are described. With regard to preferential use of the T-cell receptor (TCR), analysis of the several families of the TCR-γ gene allows rearrangement evaluation of all T cells regardless of predominant surface expression of TCR α/β. Methods: The PBMC of 10 nickel-allergic and five nonallergic individuals were cultured for 4 days in the presence of either medium, PHA, NiSO4, or tetanus toxoid (TT). Proliferation was measured by radioactive thymidine uptake and expressed as stimulation index (SI). T-cell clonality was assessed by analysis of the TCR-γ chain gene, including the use of PCR with a primer combination covering the four main groups (Vγ1-8, Vγ9, Vγ10, and Vγ11) of the variable region of the TCR-β chain gene. Results: In the allergic individuals, proliferation to NiSO4 was significantly (P〈0.05) higher than in nonallergics (mean SI: 18.05/17.87 vs 0.67/2.27). In unstimulated and PHA-stimulated cultures, there was a random TCR spectrum in both groups. In contrast, in nickel-allergic individuals or individuals with recent TT-booster, oligoclonality could be observed in the correspondingly stimulated cultures. Conclusions: In addition to proliferation assay, analysis of T-cell clonality may be a further means to characterize clinical hypersensitivity reactions on the basis of antigen-dependent oligoclonal T-cell expansion, as in the case of tissue-infiltrating lymphocytes.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 292 (2000), S. 568-569 
    ISSN: 1432-069X
    Keywords: Keywords Lichen planus ; Clonality ; Pseudolymphoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1569-8041
    Keywords: cutaneous lymphoma ; lymphoma ; R.E.A.L. Classification ; skin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background:The classification of cutaneous lymphomas has beencontroversial. The EORTC has proposed that conventional classification schemesare not suitable for cutaneous lymphomas, and that a unique classificationsystem is required. Design:The authors review the suitability of the R.E.A.L.Classification for cutaneous lymphomas, and compare it with the newly proposedEORTC system. The priniciples of the R.E.A.L. Classification have been adoptedby the WHO committees for the classification of hematopoietic and lymphoidneoplasms. Each disease is defined as a distinct entity based on anintegration of morphology, immunophenotypic and genetic features, clinicalpresentation and course, and normal cellular counterpart. If either primaryor secondary involvement of the skin is a constant factor, this aspect isconsidered integral to disease definition. Results:Organ-specific classification schemes may impede therecognition of common features of diseases involving multiple anatomic sites.For example, cutaneous marginal zone B-cell lymphomas (formerly designatedcutaneous immunocytomas) mirror the features of MALT lymphomas in otheranatomic sites. While the EORTC Classification for cutaneous lymphomasattempts to emphasize certain aspects of these neoplasms of importance todermatologists, the use of multiple classification systems is a step backward,and may lead to confusion among hematologists/oncologists, and dermatologists.Nevertheless, cutaneous lymphomas often have a more indolent natural historythan nodal lymphomas, and may require different therapeutic approaches.Clinical features are an important prognostic factor and should be utilizedin guiding therapy. For cutaneous lymphomas the presence or absence ofsystemic spread is particularly important. Additionally, the site of originis often important in the definition of disease entities. Conclusions:Organ-specific classification schemes, such as theEORTC Classification for cutaneous lymphomas, are not required, and indeed mayimpede the recognition of common features of diseases involving multipleanatomic sites. A common classification system, such as the R.E.A.L./WHOClassification, should be utilized for all lymphomas, regardless of the siteof origin.
    Type of Medium: Electronic Resource
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