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Impaired autologous mixed lymphocyte reactivity in Hodgkin's disease

Gestörte Lymphozytenreaktivität in der autologen gemischten Lymphozytenkultur bei Morbus Hodgkin

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Summary

In patients with Hodkin's disease, the impaired immune reactivity, especially of the thymus dependent system, is well established. This decreased immune response of the lymphocytes from the peripheral blood contrasts to an increased lymphocytopoiesis in the lymphatic organs with a hyperplasia of these tissues. We studied the reactivity of peripheral T lymphocytes from 20 patients with Hodgkin's disease and 26 healthy control persons against autologous and allogeneic non T cells respectively in the mixed lymphocyte culture (MLC). Our experiments show an extremely depressed autologous mixed lymphocyte reactivity (MLR) of T lymphocytes from patients with Hodgkin's disease compared to those from normal donors. In the allogeneic MLC, the proliferation of the patients' T cells was stronger than in the autologous MLC, but significantly lower than the proliferation of normal T lymphocytes when stimulated by normal non T cells. Patients' non T cells stimulated T lymphocytes from healthy donors as well as non T lymphocytes from normals did. Finally, the autologous MLR of normal lymphocytes was significantly suppressed by 18 of 23 sera from Hodgkin's patients when these sera were substituted for normal AB serum in the cultures. These results demonstrate an impaired function of T lymphocytes from patients with Hodgkin's disease in the autologous MLC and the presence of one or more factors in their serum which inhibit the proliferation of normal lymphocytes in the autologous MLC. The role of suppressor cells and their factors will be discussed.

Zusammenfassung

Die gestörte Funktion des Immunsystems, besonders die der zellulären Immunabwehr ist bei Patienten mit Morbus Hodgkin seit langem bekannt. Dabei steht der verminderten Reaktivität der peripheren Blutlymphozyten eine gesteigerte Lymphozytopoese in lymphatischen Organen mit Hyperplasie dieser Gewebe gegenüber. Wir untersuchten die Reaktivität peripherer T-Lymphozyten von 20 Patienten mit Morbus Hodgkin und 26 gesunden Kontrollpersonen gegen autologe und allogene Nicht-T-Lymphozyten in der gemischten Lymphozytenkultur (MLC). Unsere Versuche hatten folgende Ergebnisse: (1) T-Lymphozyten von Morbus Hodgkin-Patienten werden nicht oder nur sehr schwach in der autologen MLC stimuliert. (2) In der allogenen MLC reagieren T-Zellen von Patienten deutlich stärker als in der autologen MLC, jedoch significant geringer als normale T-Lymphozyten gegen normale Nicht-T-Lymphozyten. Nicht-T-Zellen von Patienten stimulieren dagegen allogene T-Lymphozyten von Gesunden kaum weniger als normale Nicht-T-Zellen. (3) Wird eine autologe MLC mit Lymphozyten gesunder Spender, jedoch mit Serum von Patienten mit Morbus Hodgkin durchgeführt, zeigt sich eine signifikante, dosisabhängige Verminderung der Reaktivität gegenüber Kontrollen mit Serum von Normalpersonen. Diese Ergebnisse zeigen zusammengefaßt bei Patienten mit Morbus Hodgkin eine gestörte Funktion der T-Lymphozyten in der autologen MLC und die Existenz eines oder mehrerer Serumfaktoren, die die Proliferation von T-Lymphozyten gesunder Personen in der autologen MLC hemmen. Die Rolle von Suppressorzellen und derer Faktoren als Ursache für diese Befunde wird diskutiert.

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Begemann, M., Claas, G. & Falke, H. Impaired autologous mixed lymphocyte reactivity in Hodgkin's disease. Klin Wochenschr 60, 19–26 (1982). https://doi.org/10.1007/BF01721583

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