IVIg Treatment Reduces Catalytic Antibody Titers of Renal Transplanted Patients
Catalytic antibodies are immunoglobulins endowed with enzymatic activity. Catalytic IgG has been reported in several human autoimmune and inflammatory diseases. In particular, low levels of catalytic IgG have been proposed as a prognostic marker for chronic allograft rejection in patients undergoing...
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Published in | PloS one Vol. 8; no. 8; p. e70731 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Public Library of Science
15.08.2013
Public Library of Science (PLoS) |
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ISSN | 1932-6203 1932-6203 |
DOI | 10.1371/journal.pone.0070731 |
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Abstract | Catalytic antibodies are immunoglobulins endowed with enzymatic activity. Catalytic IgG has been reported in several human autoimmune and inflammatory diseases. In particular, low levels of catalytic IgG have been proposed as a prognostic marker for chronic allograft rejection in patients undergoing kidney transplant. Kidney allograft is a treatment of choice for patients with end-stage renal failure. Intravenous immunoglobulins, a therapeutic pool of human IgG, is used in patients with donor-specific antibodies, alone or in conjunction with other immunosuppressive treatments, to desensitize the patients and prevent the development of acute graft rejection. Here, we followed for a period of 24 months the levels of catalytic IgG towards the synthetic peptide Pro-Phe-Arg-methylcoumarinimide in a large cohort of patients undergoing kidney transplantation. Twenty-four percent of the patients received IVIg at the time of transplantation. Our results demonstrate a marked reduction in levels of catalytic antibodies in all patients three months following kidney transplant. The decrease was significantly pronounced in patients receiving adjunct IVIg therapy. The results suggests that prevention of acute graft rejection using intravenous immunoglobulins induces a transient reduction in the levels of catalytic IgG, thus potentially jeopardizing the use of levels of catalytic antibodies as a prognosis marker for chronic allograft nephropathy. |
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AbstractList | Catalytic antibodies are immunoglobulins endowed with enzymatic activity. Catalytic IgG has been reported in several human autoimmune and inflammatory diseases. In particular, low levels of catalytic IgG have been proposed as a prognostic marker for chronic allograft rejection in patients undergoing kidney transplant. Kidney allograft is a treatment of choice for patients with end-stage renal failure. Intravenous immunoglobulins, a therapeutic pool of human IgG, is used in patients with donor-specific antibodies, alone or in conjunction with other immunosuppressive treatments, to desensitize the patients and prevent the development of acute graft rejection. Here, we followed for a period of 24 months the levels of catalytic IgG towards the synthetic peptide Pro-Phe-Arg-methylcoumarinimide in a large cohort of patients undergoing kidney transplantation. Twenty-four percent of the patients received IVIg at the time of transplantation. Our results demonstrate a marked reduction in levels of catalytic antibodies in all patients three months following kidney transplant. The decrease was significantly pronounced in patients receiving adjunct IVIg therapy. The results suggests that prevention of acute graft rejection using intravenous immunoglobulins induces a transient reduction in the levels of catalytic IgG, thus potentially jeopardizing the use of levels of catalytic antibodies as a prognosis marker for chronic allograft nephropathy. Catalytic antibodies are immunoglobulins endowed with enzymatic activity. Catalytic IgG has been reported in several human autoimmune and inflammatory diseases. In particular, low levels of catalytic IgG have been proposed as a prognostic marker for chronic allograft rejection in patients undergoing kidney transplant. Kidney allograft is a treatment of choice for patients with end-stage renal failure. Intravenous immunoglobulins, a therapeutic pool of human IgG, is used in patients with donor-specific antibodies, alone or in conjunction with other immunosuppressive treatments, to desensitize the patients and prevent the development of acute graft rejection. Here, we followed for a period of 24 months the levels of catalytic IgG towards the synthetic peptide Pro-Phe-Arg-methylcoumarinimide in a large cohort of patients undergoing kidney transplantation. Twenty-four percent of the patients received IVIg at the time of transplantation. Our results demonstrate a marked reduction in levels of catalytic antibodies in all patients three months following kidney transplant. The decrease was significantly pronounced in patients receiving adjunct IVIg therapy. The results suggests that prevention of acute graft rejection using intravenous immunoglobulins induces a transient reduction in the levels of catalytic IgG, thus potentially jeopardizing the use of levels of catalytic antibodies as a prognosis marker for chronic allograft nephropathy.Catalytic antibodies are immunoglobulins endowed with enzymatic activity. Catalytic IgG has been reported in several human autoimmune and inflammatory diseases. In particular, low levels of catalytic IgG have been proposed as a prognostic marker for chronic allograft rejection in patients undergoing kidney transplant. Kidney allograft is a treatment of choice for patients with end-stage renal failure. Intravenous immunoglobulins, a therapeutic pool of human IgG, is used in patients with donor-specific antibodies, alone or in conjunction with other immunosuppressive treatments, to desensitize the patients and prevent the development of acute graft rejection. Here, we followed for a period of 24 months the levels of catalytic IgG towards the synthetic peptide Pro-Phe-Arg-methylcoumarinimide in a large cohort of patients undergoing kidney transplantation. Twenty-four percent of the patients received IVIg at the time of transplantation. Our results demonstrate a marked reduction in levels of catalytic antibodies in all patients three months following kidney transplant. The decrease was significantly pronounced in patients receiving adjunct IVIg therapy. The results suggests that prevention of acute graft rejection using intravenous immunoglobulins induces a transient reduction in the levels of catalytic IgG, thus potentially jeopardizing the use of levels of catalytic antibodies as a prognosis marker for chronic allograft nephropathy. |
Audience | Academic |
Author | Peyron, Ivan Gilardin, Laurent Padiolleau-Lefevre, Séverine Dollinger, Cécile Friboulet, Alain Boquet, Didier Legendre, Christophe Mahendra, Ankit Thaunat, Olivier Kaveri, Srinivas V. Sharma, Meenu Wootla, Bharath Lacroix-Desmazes, Sébastien |
AuthorAffiliation | 11 Université de Lyon, Lyon, France 5 Génie Enzymatique et Cellulaire, Unité Mixte de Recherche 6022 Centre National de la Recherche Scientifique. Université de Technologie de Compiègne, Compiègne, France 9 Indian Council of Medical Research, New Delhi, India 7 Service de Transplantation Rénale et de Soins Intensifs, Hôpital Necker, Assistance publique-hôpitaux de Paris, Paris, France 10 Institut national de la santé et de la recherche médicale, U851, Lyon, France 1 Centre de Recherche des Cordeliers, Université Pierre et Marie Curie, Unité Mixte de Recherche S 872, Paris, France 8 Laboratoire international associé Institut national de la santé et de la recherche médicale, Paris, France 4 Hospices Civils de Lyon, Hôpital Edouard Herriot, Service de Transplantation, Néphrologie et Immunologie Clinique, Lyon, France 6 Institut de biologie et de technologies de Saclay, Service de Pharmacologie et d'Immunoanalyse, Laboratoire d'Ingénierie des Anticorps pour la Santé, Commissariat à l'énergie atomi |
AuthorAffiliation_xml | – name: 6 Institut de biologie et de technologies de Saclay, Service de Pharmacologie et d'Immunoanalyse, Laboratoire d'Ingénierie des Anticorps pour la Santé, Commissariat à l'énergie atomique, Saclay, Gif-sur-Yvette, France – name: 3 Institut national de la santé et de la recherche médicale U872, Paris, France – name: 5 Génie Enzymatique et Cellulaire, Unité Mixte de Recherche 6022 Centre National de la Recherche Scientifique. Université de Technologie de Compiègne, Compiègne, France – name: 11 Université de Lyon, Lyon, France – name: 2 Université Paris Descartes, Unité Mixte de Recherche S 872, Paris, France – name: 9 Indian Council of Medical Research, New Delhi, India – name: Universidade de Sao Paulo, Brazil – name: 1 Centre de Recherche des Cordeliers, Université Pierre et Marie Curie, Unité Mixte de Recherche S 872, Paris, France – name: 10 Institut national de la santé et de la recherche médicale, U851, Lyon, France – name: 7 Service de Transplantation Rénale et de Soins Intensifs, Hôpital Necker, Assistance publique-hôpitaux de Paris, Paris, France – name: 4 Hospices Civils de Lyon, Hôpital Edouard Herriot, Service de Transplantation, Néphrologie et Immunologie Clinique, Lyon, France – name: 8 Laboratoire international associé Institut national de la santé et de la recherche médicale, Paris, France |
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Copyright | COPYRIGHT 2013 Public Library of Science 2013 Mahendra et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Distributed under a Creative Commons Attribution 4.0 International License 2013 Mahendra et al 2013 Mahendra et al |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 PMCID: PMC3744545 Conceived and designed the experiments: AM CL AF DB OT SVK SLD. Performed the experiments: AM IP CD MS BW SPL. Analyzed the data: AM IP LG MS SPL OT SLD. Contributed reagents/materials/analysis tools: SPL CL. Wrote the paper: AM LG OT SLD. Competing Interests: The authors have declared that no competing interests exist. |
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Snippet | Catalytic antibodies are immunoglobulins endowed with enzymatic activity. Catalytic IgG has been reported in several human autoimmune and inflammatory... |
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SubjectTerms | Adult Aged Aged, 80 and over Antibodies Antibodies, Catalytic - blood Antibodies, Catalytic - metabolism Autoantibodies - blood Autoantibodies - immunology Biology Care and treatment Catalysis Catalytic antibodies Desensitization End-stage renal disease Engineering Sciences Enzymatic activity Enzymes Female Graft rejection Graft Rejection - immunology Health aspects Hemophilia Histocompatibility Antigens - immunology Humans Hydrolysis Immunoglobulin G Immunoglobulin G - blood Immunoglobulin G - metabolism Immunoglobulins Immunoglobulins, Intravenous - administration & dosage Immunology Immunosuppression Immunosuppressive agents Inflammatory diseases Intravenous administration Kidney diseases Kidney Transplantation Lymphocytes Male Medical prognosis Medical research Medicine Middle Aged Nephrology Nephropathy Other Patients Peptides Prognosis Reduction Rejection Renal failure Rodents Transplantation Transplants & implants Young Adult |
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Title | IVIg Treatment Reduces Catalytic Antibody Titers of Renal Transplanted Patients |
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