Selective unresponsiveness to beta cell autoantigens after induction immunosuppression in pancreas transplantation with anti-interleukin-2 receptor antibody versus anti-thymocyte globulin

التفاصيل البيبلوغرافية
العنوان: Selective unresponsiveness to beta cell autoantigens after induction immunosuppression in pancreas transplantation with anti-interleukin-2 receptor antibody versus anti-thymocyte globulin
المؤلفون: J.W. de Fijter, O. M. H. Tysma, Bart O. Roep, P. Van De Linde, Frans H.J. Claas, D.L. Roelen, P. J. M. vd Boog, J. F. Elliott
المصدر: Clinical and Experimental Immunology. 149:56-62
بيانات النشر: Oxford University Press (OUP), 2007.
سنة النشر: 2007
مصطلحات موضوعية: Adult, Graft Rejection, Male, Interleukin 2, Daclizumab, Translational Studies, medicine.medical_treatment, T cell, Immunology, Antibodies, Monoclonal, Humanized, Autoantigens, Immune system, Insulin-Secreting Cells, Immune Tolerance, Humans, Immunology and Allergy, Medicine, IL-2 receptor, Antilymphocyte Serum, Immunosuppression Therapy, business.industry, Antibodies, Monoclonal, Receptors, Interleukin-2, Immunosuppression, Middle Aged, Kidney Transplantation, Recombinant Proteins, eye diseases, CD4 Lymphocyte Count, Anti-thymocyte globulin, Transplantation, Cross-Sectional Studies, Diabetes Mellitus, Type 1, medicine.anatomical_structure, Immunoglobulin G, Interleukin-2, Female, Pancreas Transplantation, business, Immunologic Memory, Immunosuppressive Agents, medicine.drug
الوصف: Summary Pancreas transplantation in type 1 diabetes patients could result in (re)activation of allo- and autoreactive T lymphocytes. Anti-thymocyte globulin (ATG) induction treatment is a successful, but broadly reactive anti-lymphocyte therapy used in pancreas and islet transplantation. A more selective alternative is daclizumab, a monoclonal antibody directed against the interleukin-2 receptor (CD25) on activated lymphocytes. We tested the hypothesis that daclizumab is more selective and has less immunological side effects than ATG. Thirty-nine simultaneous pancreas–kidney transplantation patients with type 1 diabetes were randomized for induction therapy with ATG or daclizumab. Auto- and recall immunity was measured cross-sectionally by lymphocyte stimulation tests with a series of auto- and recall antigens in 35 successfully transplanted patients. T cell autoimmunity to islets was low in both groups, except for a marginal but significantly higher reactivity against glutamic acid decarboxylase (GAD)65 in daclizumab-treated patients. The memory responses to recall antigens were significantly higher in the daclizumab-treated group compared to ATG-treated patients, specifically against purified protein derivative (PPD) (anti-bacterial immunity), Haemophilus influenzae virus matrix protein-1 (anti-viral immunity) and p53 [anti-tumour (auto)immunity]. These data imply that daclizumab is more specifically affecting diabetes-related immune responses than ATG. The autoimmunity is affected effectively after daclizumab induction, while memory responses towards bacterial, viral and tumour antigens are preserved.
تدمد: 1365-2249
0009-9104
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe8a3b711283d56de0839712fad30e8bTest
https://doi.org/10.1111/j.1365-2249.2007.03400.xTest
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....fe8a3b711283d56de0839712fad30e8b
قاعدة البيانات: OpenAIRE