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Interleukin 2 as a potential cancer marker in patients after kidney transplantation

Transplant recipients have a significantly greater incidence of cancer, compared with the general population, who are referred to immunosuppressive therapy as an additional malignancy risk factor. Therefore, there is a need to search for an easy in clinical practice neoplasm predictor, especially fo...

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Published in:Annals of Agricultural and Environmental Medicine 2015-01, Vol.22 (2), p.320-324
Main Authors: Witkowska, Agnieszka, Zywiec, Joanna, Strozik, Agnieszka, Gorczynska-Kosiorz, Sylwia, Trautsolt, Wanda, Strzalka-Mrozik, Barbara, Kimsa, Magdalena, Owczarek, Aleksander, Stępień, Beata, Mazurek, Urszula, Grzeszczak, Władysław, Gumprecht, Janusz
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Language:English
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Summary:Transplant recipients have a significantly greater incidence of cancer, compared with the general population, who are referred to immunosuppressive therapy as an additional malignancy risk factor. Therefore, there is a need to search for an easy in clinical practice neoplasm predictor, especially for this group of patients. A group of 74 (43M and 31F; aged 46.8 ± 12 years) kidney transplant recipients was investigated in a three-year follow-up study. During the time of observation, 7 patients were diagnosed with neoplasm (7.4 ± 1.5 years after transplantation). A serum level of IL2 (ELISA test) and mRNA level of IL1beta, IL10 and TNFalfa in peripheral mononuclear blood cells - PBMCs (QRT - PCR method) were measured in every year of observation. Analysis of variances and t-Student test were used in groups mean comparison: N - patients developing malignant neoplasm group (24 probes); M - set of probes from patients with malignancies at the moment of diagnosis (11 probes); P - set of probes from patients before developing malignant neoplasm (10 probes); C - control group of healthy transplant recipients (31 probes). Among the analyzed agents, only serum IL2 level differed between the analyzed groups, with higher values in the M compared with the P group (p
ISSN:1232-1966
1898-2263
DOI:10.5604/12321966.1152087