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Intravenous immunoglobulin for the treatment of autoimmune encephalopathy in children with autism
The identification of brain-targeted autoantibodies in children with autism spectrum disorder (ASD) raises the possibility of autoimmune encephalopathy (AIE). Intravenous immunoglobulin (IVIG) is effective for AIE and for some children with ASD. Here, we present the largest case series of children w...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086890/ https://www.ncbi.nlm.nih.gov/pubmed/30097568 http://dx.doi.org/10.1038/s41398-018-0214-7 |
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author | Connery, Kathleen Tippett, Marie Delhey, Leanna M. Rose, Shannon Slattery, John C. Kahler, Stephen G. Hahn, Juergen Kruger, Uwe Cunningham, Madeleine W. Shimasaki, Craig Frye, Richard E. |
author_facet | Connery, Kathleen Tippett, Marie Delhey, Leanna M. Rose, Shannon Slattery, John C. Kahler, Stephen G. Hahn, Juergen Kruger, Uwe Cunningham, Madeleine W. Shimasaki, Craig Frye, Richard E. |
author_sort | Connery, Kathleen |
collection | PubMed |
description | The identification of brain-targeted autoantibodies in children with autism spectrum disorder (ASD) raises the possibility of autoimmune encephalopathy (AIE). Intravenous immunoglobulin (IVIG) is effective for AIE and for some children with ASD. Here, we present the largest case series of children with ASD treated with IVIG. Through an ASD clinic, we screened 82 children for AIE, 80 of them with ASD. IVIG was recommended for 49 (60%) with 31 (38%) receiving the treatment under our care team. The majority of parents (90%) reported some improvement with 71% reporting improvements in two or more symptoms. In a subset of patients, Aberrant Behavior Checklist (ABC) and/or Social Responsiveness Scale (SRS) were completed before and during IVIG treatment. Statistically significant improvement occurred in the SRS and ABC. The antidopamine D2L receptor antibody, the anti-tubulin antibody and the ratio of the antidopamine D2L to D1 receptor antibodies were related to changes in the ABC. The Cunningham Panel predicted SRS, ABC, parent-based treatment responses with good accuracy. Adverse effects were common (62%) but mostly limited to the infusion period. Only two (6%) patients discontinued IVIG because of adverse effects. Overall, our open-label case series provides support for the possibility that some children with ASD may benefit from IVIG. Given that adverse effects are not uncommon, IVIG treatment needs to be considered cautiously. We identified immune biomarkers in select IVIG responders but larger cohorts are needed to study immune biomarkers in more detail. Our small open-label exploratory trial provides evidence supporting a neuroimmune subgroup in patients with ASD. |
format | Online Article Text |
id | pubmed-6086890 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60868902018-08-13 Intravenous immunoglobulin for the treatment of autoimmune encephalopathy in children with autism Connery, Kathleen Tippett, Marie Delhey, Leanna M. Rose, Shannon Slattery, John C. Kahler, Stephen G. Hahn, Juergen Kruger, Uwe Cunningham, Madeleine W. Shimasaki, Craig Frye, Richard E. Transl Psychiatry Article The identification of brain-targeted autoantibodies in children with autism spectrum disorder (ASD) raises the possibility of autoimmune encephalopathy (AIE). Intravenous immunoglobulin (IVIG) is effective for AIE and for some children with ASD. Here, we present the largest case series of children with ASD treated with IVIG. Through an ASD clinic, we screened 82 children for AIE, 80 of them with ASD. IVIG was recommended for 49 (60%) with 31 (38%) receiving the treatment under our care team. The majority of parents (90%) reported some improvement with 71% reporting improvements in two or more symptoms. In a subset of patients, Aberrant Behavior Checklist (ABC) and/or Social Responsiveness Scale (SRS) were completed before and during IVIG treatment. Statistically significant improvement occurred in the SRS and ABC. The antidopamine D2L receptor antibody, the anti-tubulin antibody and the ratio of the antidopamine D2L to D1 receptor antibodies were related to changes in the ABC. The Cunningham Panel predicted SRS, ABC, parent-based treatment responses with good accuracy. Adverse effects were common (62%) but mostly limited to the infusion period. Only two (6%) patients discontinued IVIG because of adverse effects. Overall, our open-label case series provides support for the possibility that some children with ASD may benefit from IVIG. Given that adverse effects are not uncommon, IVIG treatment needs to be considered cautiously. We identified immune biomarkers in select IVIG responders but larger cohorts are needed to study immune biomarkers in more detail. Our small open-label exploratory trial provides evidence supporting a neuroimmune subgroup in patients with ASD. Nature Publishing Group UK 2018-08-10 /pmc/articles/PMC6086890/ /pubmed/30097568 http://dx.doi.org/10.1038/s41398-018-0214-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Connery, Kathleen Tippett, Marie Delhey, Leanna M. Rose, Shannon Slattery, John C. Kahler, Stephen G. Hahn, Juergen Kruger, Uwe Cunningham, Madeleine W. Shimasaki, Craig Frye, Richard E. Intravenous immunoglobulin for the treatment of autoimmune encephalopathy in children with autism |
title | Intravenous immunoglobulin for the treatment of autoimmune encephalopathy in children with autism |
title_full | Intravenous immunoglobulin for the treatment of autoimmune encephalopathy in children with autism |
title_fullStr | Intravenous immunoglobulin for the treatment of autoimmune encephalopathy in children with autism |
title_full_unstemmed | Intravenous immunoglobulin for the treatment of autoimmune encephalopathy in children with autism |
title_short | Intravenous immunoglobulin for the treatment of autoimmune encephalopathy in children with autism |
title_sort | intravenous immunoglobulin for the treatment of autoimmune encephalopathy in children with autism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086890/ https://www.ncbi.nlm.nih.gov/pubmed/30097568 http://dx.doi.org/10.1038/s41398-018-0214-7 |
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