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Immune reconstitution, glomerulonephritis, and successful treatment with rituximab

Background: Alemtuzumab can induce secondary autoimmunity affecting multiple organs. While kidney involvement is uncommon, it can be associated with devastating forms of glomerulonephritis (GN). Case presentation: A 32-year-old African American woman presented with hypertension, proteinuria, and pro...

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Autores principales: Vasquez-Rios, George, Edwards, John C., Tummala, Saketh, Chapel, Ashley, Sunna, Ramez, Brink, David S., Laohathai, Christopher, Vo, Thanh-Mai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dustri-Verlag Dr. Karl Feistle 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469242/
https://www.ncbi.nlm.nih.gov/pubmed/32905274
http://dx.doi.org/10.5414/CNCS110061
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author Vasquez-Rios, George
Edwards, John C.
Tummala, Saketh
Chapel, Ashley
Sunna, Ramez
Brink, David S.
Laohathai, Christopher
Vo, Thanh-Mai
author_facet Vasquez-Rios, George
Edwards, John C.
Tummala, Saketh
Chapel, Ashley
Sunna, Ramez
Brink, David S.
Laohathai, Christopher
Vo, Thanh-Mai
author_sort Vasquez-Rios, George
collection PubMed
description Background: Alemtuzumab can induce secondary autoimmunity affecting multiple organs. While kidney involvement is uncommon, it can be associated with devastating forms of glomerulonephritis (GN). Case presentation: A 32-year-old African American woman presented with hypertension, proteinuria, and progressive renal failure. Her medical history was remarkable for secondary progressive multiple sclerosis (SPMS). She had received her first induction dose of alemtuzumab 1 year prior to presentation. Upon evaluation, she had scanning speech, multidirectional nystagmus, and mild edema. Her serum creatinine was 2 mg/dL. Urine studies revealed proteinuria and microscopic hematuria. Her serologic tests were positive for c-antineutrophil cytoplasmic antibodies (> 1 : 640). In addition, she was found to have new-onset severe thyroid dysfunction with antibodies against thyroglobulin and thyroid peroxidase. Kidney biopsy was diagnostic for pauci-immune crescentic GN. The patient was treated with methylprednisolone and rituximab with subsequent renal, thyroid, and neurological recovery. Conclusion: This is an atypical case of GN following therapy with alemtuzumab. We hypothesize that immune reconstitution may be a potential mechanism. Alemtuzumab is a new treatment for SPMS that can be associated with GN. Practice guidelines should address the management of its renal complications.
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spelling pubmed-74692422020-09-03 Immune reconstitution, glomerulonephritis, and successful treatment with rituximab Vasquez-Rios, George Edwards, John C. Tummala, Saketh Chapel, Ashley Sunna, Ramez Brink, David S. Laohathai, Christopher Vo, Thanh-Mai Clin Nephrol Case Stud Case Report Background: Alemtuzumab can induce secondary autoimmunity affecting multiple organs. While kidney involvement is uncommon, it can be associated with devastating forms of glomerulonephritis (GN). Case presentation: A 32-year-old African American woman presented with hypertension, proteinuria, and progressive renal failure. Her medical history was remarkable for secondary progressive multiple sclerosis (SPMS). She had received her first induction dose of alemtuzumab 1 year prior to presentation. Upon evaluation, she had scanning speech, multidirectional nystagmus, and mild edema. Her serum creatinine was 2 mg/dL. Urine studies revealed proteinuria and microscopic hematuria. Her serologic tests were positive for c-antineutrophil cytoplasmic antibodies (> 1 : 640). In addition, she was found to have new-onset severe thyroid dysfunction with antibodies against thyroglobulin and thyroid peroxidase. Kidney biopsy was diagnostic for pauci-immune crescentic GN. The patient was treated with methylprednisolone and rituximab with subsequent renal, thyroid, and neurological recovery. Conclusion: This is an atypical case of GN following therapy with alemtuzumab. We hypothesize that immune reconstitution may be a potential mechanism. Alemtuzumab is a new treatment for SPMS that can be associated with GN. Practice guidelines should address the management of its renal complications. Dustri-Verlag Dr. Karl Feistle 2020-09-01 /pmc/articles/PMC7469242/ /pubmed/32905274 http://dx.doi.org/10.5414/CNCS110061 Text en © Dustri-Verlag Dr. K. Feistle http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Vasquez-Rios, George
Edwards, John C.
Tummala, Saketh
Chapel, Ashley
Sunna, Ramez
Brink, David S.
Laohathai, Christopher
Vo, Thanh-Mai
Immune reconstitution, glomerulonephritis, and successful treatment with rituximab
title Immune reconstitution, glomerulonephritis, and successful treatment with rituximab
title_full Immune reconstitution, glomerulonephritis, and successful treatment with rituximab
title_fullStr Immune reconstitution, glomerulonephritis, and successful treatment with rituximab
title_full_unstemmed Immune reconstitution, glomerulonephritis, and successful treatment with rituximab
title_short Immune reconstitution, glomerulonephritis, and successful treatment with rituximab
title_sort immune reconstitution, glomerulonephritis, and successful treatment with rituximab
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469242/
https://www.ncbi.nlm.nih.gov/pubmed/32905274
http://dx.doi.org/10.5414/CNCS110061
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