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Biomedical subjects

U Mey

Publications and source records attributed to U Mey.

At least 37 records · Page 2Linked to original sources

[The spleen--still a puzzling organ?].

The model of animal experiments developed in the sixties by the Erfurt investigation team of A. Sundermann, according to which autoimmunisation phenomena may be evoked in the rabbit by the application of warmth-alterated autologous blood cells, undergoes a repeated critical consideration on the basis of the modern knowledge of the nature of the autoimmunisation process. In this case must be stated that the importance of the spleen for the development of such processes is finally still unclear. The favourable therapeutical effects of a splenectomy observed in the model and also in clinical routine work cannot be explained sufficiently theoretically, particularly on the basis of the recent results of research concerning the cellular immune mechanisms. No doubt, it seems to be clear that the spleen is authoritatively responsible for the primary immune response, however it remains questionable, whether an isolated primary response is really existing, since on its part it already depends on T-lymphocytes which stimulate the secondary response. However, a splenectomy might be suitable theoretically--if at all--for the interruption of the immune process only in the stage of the primary reaction. In the complex process within the immune response with the various implications between B- and T-lymphocytes and the increasing knowledge of the counter-regulating humoral and cellular control mechanisms the picture of the importance of the spleen seeming to be more distinct in the intervening time becomes again more indistinct. Thus the spleen for the time being remains the enigmatical organ, as it was characterized by Sundermann already for more than ten years ago.

Animals↗

[Acute mature myelocytic leukemia as a form of the myeloproliferative syndrome].

On the basis of five observations of adult patients with the clinical feature of mature cellular leukaemia which proved to be therapy-refractory and which was characterized by a rapid course is referred to the necessity of the differentiation of such cases from the classical myeloic leukaemia. The cardinal symptoms of this type of disease, which probably is identified with the cases described in literature as atypical chronic myelosis, as paraneutrophil leukaemia or as acute myelofibrosis, and also shows common features with the juvenile chronic myelosis, are, apart from the mature cellular differential blood picture a short life expectancy (less than 1 year), an initial thrombocytopenia, a normal or increased activity of the alkaline granulocyte phosphatase, the lack of Ph1-chromosome as well as the bad therapeutic reaction to busulfan. The observation of the simultaneously existing fibroses of the bone marrow as well as of the final increase of immature blasts induced the classification of the clinical picture as a special form of the myeloproliferative syndrome.

Acute Disease↗

[Immunology and oncology of paraproteins].

Since the first description by Apitz paraproteins were for a long time regarded as biologically abnormal proteins which normally do not appear in the human plasma. According to the modern biochemical knowledge this determination of the notion can no more be acknowledged, since analyses of amino acids did not reveal any differences in the composition of the complete paraproteins and the immune globulins. Apart from the complete paraproteins which consist either of gamma, my, delta, alpha or epsilon heavy chains on the one hand and of kappa or lambda easy chains on the other hand, also molecule fragments and isolated heavy or easy chains, respectively, appear. Like immune proteins paraproteins are formed by B-lymphocytes and their transformation forms, respectively, in which case the monoclonality represents their specific characteristic. Thus exist close relations to malignant changes of the B-lymphocyte system, in particular to the non-Hodgkin-lymphomas. Several functional peculiarities of the paraproteins, such as autoantibody effect, lymphocytotoxicity, aggregation ability and binding affinity to blood cells lead to multiform clinical phenomena. To this belong immune defects, nephropathies, haemocytopenias, amyloidoses and haemorrhagic diatheses. As evoking cause of the alteration of B-lymphocyte system with activation of one or several cell clones (e.g. in double paraproteinaemia) tumour viruses are taken into consideration. After an infection with oncogenic herpes viruses irreversible cell transformations in the lymphatic system have been proved. Thus it is doubtful, whether there are indeed true benign paraproteinaemias. One has rather to speak only of relatively benign forms of the course.

Animals↗

[Studies on cell-mediated immunity in patients with chronic lymphatic leukemia].

More than 100,000 variables (anamnestic, clinical, serological, radiological and histological individual findings) of 142 patients with rheumatoid arthritis underwent a factor analysis. In the calculatory statistical course by means of information densification we established a few basic variables, called factors. The interpretation of these factors showed apart from logical and pathogenetic connection also relations which gave an impetus for further clinical research.

Aged↗

[Chronic lymphadenosis--short review].

It was tried to show in form of a survey some molecular-biological, immunopathological and kinetic aspects of the CL (chronic lymphadenosis)-lymphocytes, which seem to be significant for the pathogenesis of chronic lymphadenosis. Apart from this, the modern therapeutic possibilities concerning the inhibition of proliferation as well as the depletion which seem to be suitable for influencing the still fatal course of chronic lymphadenosis are discussed.

Antibody Formation↗