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Featured researches published by Tibor Bakács.


Cancer | 1981

Angioimmunoblastic lymphadenopathy: A study of the function of lymphocyte populations

T. Garam; Mihály Bak; Tibor Bakács; Eszter Döbrentei; Győző Petrányi

The case of a 57‐year‐old woman with the diagnosis of angioimmunoblastic lymphadenopathy (AILD) is reported. During the 15 years of the disease, no malignant transformation had been detected. The clinical picture is unusual in certain respects. Lymph node manifestation had been preceded by extraglandular AILD infiltrates. All histologic materials showed a picture typical of AILD. A functional study of peripheral lymphocyte subpopulations revealed decreased natural cytotoxicity and decreased T‐lymphocyte activity.


Cancer Immunology, Immunotherapy | 1984

Enhanced K-cell activity in the peripheral blood of patients with malignant disease

Tibor Bakács; Pál Czanik; Ian Kimber; Gábor Ringwald; Michael Moore; Erzsébet Ábrahám

SummaryWe have analysed the influence of human malignant, inflammatory and infectious disease on the capacity of peripheral lymphocytes to mediate antibody-dependent haemolysis. The application of an enzyme-like kinetic model for measurement of maximal cytotoxic function has permitted reproducible and sensitive determinations of the K-cell function. The results show that malignant disease is associated with enhancement of ADCC capacity.


British Journal of Haematology | 1984

K cell mediated haemolysis: influence of large numbers of unsensitized cells on the antibody-dependent lysis of anti-D-sensitized erythrocytes by human lymphocytes.

Tibor Bakács; Ian Kimber; Gábor Ringwald; Michael Moore

Summary. The inhibition of K cell mediated haemolysis of anti‐D‐sensitized human red blood cells by unsensitized erythrocytes has been demonstrated. Inhibition of lysis was non‐competitive in nature and influenced by the size and number of unsensitized cells. However, even in the presence of high inhibitor: target cell ratios (50:1) haemolysis, although reduced, was still effected suggesting that K cells are highly motile and capable of recognizing and destroying minority populations of antibody‐sensitized erythrocytes. These data are compatible with a role for cytotoxic lymphocytes in the intravascular lysis of autoantibody or alloantibody‐sensitized red cells.


Immunology Letters | 1982

Direct ADCC lysis of O,Rh-positive (R1R2) erythrocytes by lymphocytes of individuals sensitized against antigen D

Tibor Bakács; Gábor Ringwald; Ilona Jókuti

Non-T-cells from individuals sensitized against antigen D were found to lyze O,Rh-positive erythrocytes. The lytic effect was abolished by incubation of the effector cells at 37 degrees C for 30 min, and was reconstituted by addition of anti-D antibodies. These results suggested that sensitized donors have lymphocytes armed with specific antibodies in vivo.


Vox Sanguinis | 1989

The Role of Antibody Density in the Immune Lysis of Sensitised Erythrocytes: A Mathematical Appreciation

Tibor Bakács; Gábor Ringwald; Tünde Léránth; Ian Kimber

Abstract. The influence of sensitizing antibody density on target cell selection by effector monocytes was examined by modifying the sensitization of red cells either by dilution of the antiserum, variation of the number of erythrocytes or both in a cold target competition assay of antibody‐dependent cellular cytotoxicity (ADCC). Human A1 and B erythrocyte target and competitor cells were employed in the presence of hyperimmune anti‐A and anti‐B sera at concentrations above that necessary for saturation of red cells with respect to lytic susceptibility. When the number of red cells was kept constant and the dilution of antisera was varied a linear relationship between the competitive capacity of erythrocytes and the concentration of sensitizing antiserum was observed. When the number of target (competitor) cells and the concentration of antisera were varied simultaneously it was apparent that the competitive capacity was dependent upon the relative densities of the sensitizing antibodies. When competition was tested in the presence of suboptimal concentrations of complement, rather than effector cells it was observed that, in common with ADCC, the effectiveness of cold competition was dependent upon the concentration of sensitizing antibody.


NK Cells and Other Natural Effector Cells | 1982

NK AND K CELL ACTIVITY IN MAMMARY AND CERVIX CARCINOMA PATIENTS IN RELATION TO RADIATION THERAPY AND THE COURSE OF DISEASE

T. Garam; Tamás Pulay; Tibor Bakács; Egon Svastits; Gábor Ringwald; Klára Tótpál; Győző Petrányi

Publisher Summary This chapter reviews natural killer (NK)- and K-cell activity in mammary and cervix carcinoma patients in relation to radiation therapy and the course of disease. In a study described in the chapter, 79 patients with mammary tumors and 40 cervical cancer patients were tested before and after surgical and X-ray therapy. The patients were categorized in stage I–IV according to the definition of UICC and FIGO. The patients were not given antitumor therapy before the surgical intervention. The control group consisted of 70 healthy women. Two methods were used for examining cytotoxicity with the lymphocytes separated from the peripheral blood. One of them was the conventional cytitoxic assay and the other method was the cytotoxic capacity test. The data obtained show a general decrease of the NK- and K-cell activity of mammary carcinoma patients and a decrease of the NK-cell activity of cervix carcinoma patients, in comparison with the healthy controls. Irradiation did not influence the NK- and K-cell function in comparison to the values obtained before radiotherapy. NK activity is increased by average of 72.6% by the serum of mammary tumor patients and 41.6% by the serum of cervix carcinoma patients.


Immunology Letters | 1982

Inhibition of the anti-D antibody-dependent cellular cytotoxicity against O,Rh-positive (R1R2) erythrocytes by O,Rh-negative (rr) competitor cells

Tibor Bakács; Gábor Ringwald; Károly Wedrödy

Anti-D antibody-dependent lymphocyte-mediated lysis of O,Rh-positive (R1R2) erythrocytes was inhibited by O,Rh-negative (rr) erythrocytes in cold target competition experiments. The degree of inhibitory effects was different with the different antisera used for sensitization. Under the same conditions the inhibition varied between 23 and 79%. The difference did not relate to the titres of the sera.


Vox Sanguinis | 1989

The Role of Antibody Density in the Immune Lysis of Sensitised Erythrocytes

Tibor Bakács; Gábor Ringwald; Tünde Léránth; Ian Kimber

The influence of sensitizing antibody density on target cell selection by effector monocytes was examined by modifying the sensitization of red cells either by dilution of the antiserum, variation of the number of erythrocytes or both in a cold target competition assay of antibody-dependent cellular cytotoxicity (ADCC). Human A1 and B erythrocyte target and competitor cells were employed in the presence of hyperimmune anti-A and anti-B sera at concentrations above that necessary for saturation of red cells with respect to lytic susceptibility. When the number of red cells was kept constant and the dilution of antisera was varied a linear relationship between the competitive capacity of erythrocytes and the concentration of sensitizing antiserum was observed. When the number of target (competitor) cells and the concentration of antisera were varied simultaneously it was apparent that the competitive capacity was dependent upon the relative densities of the sensitizing antibodies. When competition was tested in the presence of suboptimal concentrations of complement, rather than effector cells it was observed that, in common with ADCC, the effectiveness of cold competition was dependent upon the concentration of sensitizing antibody.


Clinical and Experimental Immunology | 1983

Regulation of natural and antibody-dependent cellular cytotoxicity by staphylococcal enterotoxin A

Ian Kimber; Tibor Bakács; Michael Moore


Journal of clinical & laboratory immunology | 1984

Influence of lectin-free interleukin-2 on natural and antibody-dependent cellular cytotoxicity.

Ian Kimber; Tibor Bakács; Kevan Roberts; Michael Moore

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Ian Kimber

University of Manchester

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Michael Moore

Plymouth Marine Laboratory

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T. Garam

Semmelweis University

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Gergely P

Semmelweis University

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