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Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody
An 80-year-old woman with malignant melanoma received 20 cycles of anti-programmed death 1 (PD-1) antibody (nivolumab) treatment and showed normal glucose tolerance. Three weeks after switching to anti-cytotoxic T-lymphocyte associated antigen 4 (CTLA-4) antibody (ipilimumab), her plasma glucose lev...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society of Internal Medicine
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096029/ https://www.ncbi.nlm.nih.gov/pubmed/29491310 http://dx.doi.org/10.2169/internalmedicine.9518-17 |
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author | Shiba, Michiru Inaba, Hidefumi Ariyasu, Hiroyuki Kawai, Shintaro Inagaki, Yuko Matsuno, Shohei Iwakura, Hiroshi Yamamoto, Yuki Nishi, Masahiro Akamizu, Takashi |
author_facet | Shiba, Michiru Inaba, Hidefumi Ariyasu, Hiroyuki Kawai, Shintaro Inagaki, Yuko Matsuno, Shohei Iwakura, Hiroshi Yamamoto, Yuki Nishi, Masahiro Akamizu, Takashi |
author_sort | Shiba, Michiru |
collection | PubMed |
description | An 80-year-old woman with malignant melanoma received 20 cycles of anti-programmed death 1 (PD-1) antibody (nivolumab) treatment and showed normal glucose tolerance. Three weeks after switching to anti-cytotoxic T-lymphocyte associated antigen 4 (CTLA-4) antibody (ipilimumab), her plasma glucose level was elevated to 639 mg/dL, her HbA1c was 7.7%, and her fastening serum C-peptide immunoreactivity was undetectable. Anti-glutamic acid decarboxylase and insulinoma-associated protein-2 antibodies were negative. She was diagnosed with fulminant type 1 diabetes mellitus (F1DM). Remarkably, her anti-insulin antibody was positively converted, and her Sialylated Carbohydrate Antigen, Krebs von den Lungen-6 levels increased after ipilimumab therapy. She possessed F1DM-susceptible Human Leukocyte Antigen-DR4. A fluorescence activated cell sorting analysis showed an altered T-cell population. This case of F1DM highlights specific mechanisms underlying pancreatic beta cell immunity. |
format | Online Article Text |
id | pubmed-6096029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Japanese Society of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-60960292018-08-17 Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody Shiba, Michiru Inaba, Hidefumi Ariyasu, Hiroyuki Kawai, Shintaro Inagaki, Yuko Matsuno, Shohei Iwakura, Hiroshi Yamamoto, Yuki Nishi, Masahiro Akamizu, Takashi Intern Med Case Report An 80-year-old woman with malignant melanoma received 20 cycles of anti-programmed death 1 (PD-1) antibody (nivolumab) treatment and showed normal glucose tolerance. Three weeks after switching to anti-cytotoxic T-lymphocyte associated antigen 4 (CTLA-4) antibody (ipilimumab), her plasma glucose level was elevated to 639 mg/dL, her HbA1c was 7.7%, and her fastening serum C-peptide immunoreactivity was undetectable. Anti-glutamic acid decarboxylase and insulinoma-associated protein-2 antibodies were negative. She was diagnosed with fulminant type 1 diabetes mellitus (F1DM). Remarkably, her anti-insulin antibody was positively converted, and her Sialylated Carbohydrate Antigen, Krebs von den Lungen-6 levels increased after ipilimumab therapy. She possessed F1DM-susceptible Human Leukocyte Antigen-DR4. A fluorescence activated cell sorting analysis showed an altered T-cell population. This case of F1DM highlights specific mechanisms underlying pancreatic beta cell immunity. The Japanese Society of Internal Medicine 2018-02-28 2018-07-15 /pmc/articles/PMC6096029/ /pubmed/29491310 http://dx.doi.org/10.2169/internalmedicine.9518-17 Text en Copyright © 2018 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Shiba, Michiru Inaba, Hidefumi Ariyasu, Hiroyuki Kawai, Shintaro Inagaki, Yuko Matsuno, Shohei Iwakura, Hiroshi Yamamoto, Yuki Nishi, Masahiro Akamizu, Takashi Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody |
title | Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody |
title_full | Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody |
title_fullStr | Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody |
title_full_unstemmed | Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody |
title_short | Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody |
title_sort | fulminant type 1 diabetes mellitus accompanied by positive conversion of anti-insulin antibody after the administration of anti-ctla-4 antibody following the discontinuation of anti-pd-1 antibody |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096029/ https://www.ncbi.nlm.nih.gov/pubmed/29491310 http://dx.doi.org/10.2169/internalmedicine.9518-17 |
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