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Autologous Stem Cell Transplantation in Common Variable Immunodeficiency: A Case of Successful Treatment of Severe Refractory Autoimmune Encephalitis
Common variable immunodeficiency (CVID) is the most common primary immunodeficiency in adults. It is associated with hypogammaglobulinemia, recurring infections and autoimmune phenomena. Treatment includes immunoglobulin substitution and immunosuppressants. Autoimmune neurological manifestations of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330058/ https://www.ncbi.nlm.nih.gov/pubmed/32670291 http://dx.doi.org/10.3389/fimmu.2020.01317 |
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author | Froehlich, Matthias Schwaneck, Eva C. Gernert, Michael Gadeholt, Ottar Strunz, Patrick-Pascal Morbach, Henner Tony, Hans-Peter Schmalzing, Marc |
author_facet | Froehlich, Matthias Schwaneck, Eva C. Gernert, Michael Gadeholt, Ottar Strunz, Patrick-Pascal Morbach, Henner Tony, Hans-Peter Schmalzing, Marc |
author_sort | Froehlich, Matthias |
collection | PubMed |
description | Common variable immunodeficiency (CVID) is the most common primary immunodeficiency in adults. It is associated with hypogammaglobulinemia, recurring infections and autoimmune phenomena. Treatment includes immunoglobulin substitution and immunosuppressants. Autoimmune neurological manifestations of CVID are rare and occur predominantly as granulomatous disease. We report the case of a 35-year-old woman with CVID who developed autoimmune encephalitis as demonstrated by double cerebral biopsy. Infectious or malignant causes could be excluded. Despite intensive immunosuppressive therapy with common regimens no significant improvement could be achieved. Ultimately, an autologous hematopoietic stem cell transplantation (HSCT) was performed, resulting in lasting complete remission of the encephalitis. To our knowledge, this is the first report of refractory autoimmune phenomena in CVID treated by autologous HSCT. |
format | Online Article Text |
id | pubmed-7330058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73300582020-07-14 Autologous Stem Cell Transplantation in Common Variable Immunodeficiency: A Case of Successful Treatment of Severe Refractory Autoimmune Encephalitis Froehlich, Matthias Schwaneck, Eva C. Gernert, Michael Gadeholt, Ottar Strunz, Patrick-Pascal Morbach, Henner Tony, Hans-Peter Schmalzing, Marc Front Immunol Immunology Common variable immunodeficiency (CVID) is the most common primary immunodeficiency in adults. It is associated with hypogammaglobulinemia, recurring infections and autoimmune phenomena. Treatment includes immunoglobulin substitution and immunosuppressants. Autoimmune neurological manifestations of CVID are rare and occur predominantly as granulomatous disease. We report the case of a 35-year-old woman with CVID who developed autoimmune encephalitis as demonstrated by double cerebral biopsy. Infectious or malignant causes could be excluded. Despite intensive immunosuppressive therapy with common regimens no significant improvement could be achieved. Ultimately, an autologous hematopoietic stem cell transplantation (HSCT) was performed, resulting in lasting complete remission of the encephalitis. To our knowledge, this is the first report of refractory autoimmune phenomena in CVID treated by autologous HSCT. Frontiers Media S.A. 2020-06-25 /pmc/articles/PMC7330058/ /pubmed/32670291 http://dx.doi.org/10.3389/fimmu.2020.01317 Text en Copyright © 2020 Froehlich, Schwaneck, Gernert, Gadeholt, Strunz, Morbach, Tony and Schmalzing. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Froehlich, Matthias Schwaneck, Eva C. Gernert, Michael Gadeholt, Ottar Strunz, Patrick-Pascal Morbach, Henner Tony, Hans-Peter Schmalzing, Marc Autologous Stem Cell Transplantation in Common Variable Immunodeficiency: A Case of Successful Treatment of Severe Refractory Autoimmune Encephalitis |
title | Autologous Stem Cell Transplantation in Common Variable Immunodeficiency: A Case of Successful Treatment of Severe Refractory Autoimmune Encephalitis |
title_full | Autologous Stem Cell Transplantation in Common Variable Immunodeficiency: A Case of Successful Treatment of Severe Refractory Autoimmune Encephalitis |
title_fullStr | Autologous Stem Cell Transplantation in Common Variable Immunodeficiency: A Case of Successful Treatment of Severe Refractory Autoimmune Encephalitis |
title_full_unstemmed | Autologous Stem Cell Transplantation in Common Variable Immunodeficiency: A Case of Successful Treatment of Severe Refractory Autoimmune Encephalitis |
title_short | Autologous Stem Cell Transplantation in Common Variable Immunodeficiency: A Case of Successful Treatment of Severe Refractory Autoimmune Encephalitis |
title_sort | autologous stem cell transplantation in common variable immunodeficiency: a case of successful treatment of severe refractory autoimmune encephalitis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330058/ https://www.ncbi.nlm.nih.gov/pubmed/32670291 http://dx.doi.org/10.3389/fimmu.2020.01317 |
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