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Biomedical subjects

Dieter Kabelitz

Publications and source records attributed to Dieter Kabelitz.

39 records · Page 3Linked to original sources

Reciprocal alterations of Th1/Th2 function in gammadelta T-cell subsets of human immunodeficiency virus-1-infected patients.

While T cells that express Vgamma9 as a variable T-cell receptor chain dominate among peripheral blood gammadelta T cells in healthy adults, Vdelta1 cells are the major subpopulation of gammadelta T cells in human immunodeficiency virus (HIV)-infected patients. We used intracellular cytokine staining and flow cytometry to analyse whether an imbalance of T helper 1 (Th1)/T helper 2 (Th2) cytokine patterns, as observed in alphabeta T cells, also occurs in gammadelta T cells. When compared with healthy HIV-negative subjects, HIV+ patients had a decreased number of interferon-gamma (IFN-gamma)+gammadelta T cells, which showed a linear relation to the CD4+ cell count but not to the plasma viral load. Similar results were obtained when Vgamma9 cells were analysed. In contrast, in the Vdelta1 subpopulation, the number of IFN-gamma+ cells was increased in HIV+ donors when compared with healthy subjects. Even though less impressive, the number of interleukin 4 (IL-4)- and IL-10-producing cells was uniformly inversely correlated with the number of tumour necrosis factor-alpha+ and IFN-gamma+ cells. The increased IFN-gamma-producing capacity of Vdelta1 cells might represent a compensatory mechanism for the progressive loss of Vgamma9 gammadelta T cells during the course of HIV infection.

Adolescent↗

Synergism between lectins and vesicles of Viscum album L.- detection by biochemical and immunological methods.

Mistletoe (Viscum album L.) extracts, used in cancer therapy, contain several antitumor and immunologically active ingredients of which the cytotoxic mistletoe lectins and the immunoactive vesicles of chloroplast membranes are particularly important. We have investigated interactions between vesicles and lectins with respect to the question of synergistic or antagonistic effects. First we used biochemical methods. Lectin binding to vesicles was dependent on the pH-value and ionic strength of the buffers used. The strongest interaction was observed at low pH-values and at low ionic strength. Using immunological methods, we found that the combination of lectins and vesicles showed a strong amplifying synergistic effect on the stimulation of lymphocyte proliferation. We found an antagonistic effect in terms of cytotoxicity. In summary, these results demonstrate a significant influence of vesicles on all commonly used methods of determination of mistletoe lectins.

Journal Article↗

[Potency testing of anti-lymphocyte Globulins: In vitro alternatives for the monkey skin-graft assay]

Antilymphocyte globulins (ALG) are immunosuppressive agents of animal origin currently used in clinical transplantation medicine and for the treatment of severe aplastic anemia. The potency of each batch is tested in vivo using primates as hosts for allogeneic skin transplantation. The test is done with a maximum of three animals, one as a control and two after the treatment with ALG. The two in vitro methods in use are a cytotoxic assay and the rosette inhibition assay. These methods are evaluated with the microscope. Besides wellfare aspects these methods require a lot of experience, are subjective, difficult to validate and the information about the biological potency of the sera is questionable. The aim of our study is a better biological characterisation as a prerequisite to subsequently define an in vitro alternative for the potency test in monkeys. Using a competition assay with monoclonal antibodies we can identify several specificities directed against functional molecules on T cells (e.g., CD2, CD3, CD5, CD28), B Cells (CD19), macrophages and natural killer cells (CD16) and nonlineage specificities such as CD18, CD25, CD29, CD95. This method could describe a part of the biological potency and control homogeneity of batches. The cytotoxic capacity of ALG either with or without complement as well as DNA-fragmentation characteristic for apoptosis can be analysed by flowcytometry using propidiumiodide- (PI) incorporation. Immunoprecipitation of cell-lysate with ALG<<s and subsequent incubation with radioactive ATP (kinase-assay) shows specific bands which seem to be identical between different batches of one product.

Journal Article↗