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Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency
BACKGROUND: Patients with an IgG subclass deficiency (IgSD) ± specific polysaccharide antibody deficiency (SPAD) often present with recurrent infections. Previous retrospective studies have shown that prophylactic antibiotics (PA) and immunoglobulin replacement therapy (IRT) can both be effective in...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858555/ https://www.ncbi.nlm.nih.gov/pubmed/33206257 http://dx.doi.org/10.1007/s10875-020-00841-3 |
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author | Smits, Bas M. Kleine Budde, Ilona de Vries, Esther ten Berge, Ineke J. M. Bredius, Robbert G. M. van Deuren, Marcel van Dissel, Jaap T. Ellerbroek, Pauline M. van der Flier, Michiel van Hagen, P. Martin Nieuwhof, Chris Rutgers, Bram Sanders, Lieke E. A. M. Simon, Anna Kuijpers, Taco W. van Montfrans, Joris M. |
author_facet | Smits, Bas M. Kleine Budde, Ilona de Vries, Esther ten Berge, Ineke J. M. Bredius, Robbert G. M. van Deuren, Marcel van Dissel, Jaap T. Ellerbroek, Pauline M. van der Flier, Michiel van Hagen, P. Martin Nieuwhof, Chris Rutgers, Bram Sanders, Lieke E. A. M. Simon, Anna Kuijpers, Taco W. van Montfrans, Joris M. |
author_sort | Smits, Bas M. |
collection | PubMed |
description | BACKGROUND: Patients with an IgG subclass deficiency (IgSD) ± specific polysaccharide antibody deficiency (SPAD) often present with recurrent infections. Previous retrospective studies have shown that prophylactic antibiotics (PA) and immunoglobulin replacement therapy (IRT) can both be effective in preventing these infections; however, this has not been confirmed in a prospective study. OBJECTIVE: To compare the efficacy of PA and IRT in a randomized crossover trial. METHODS: A total of 64 patients (55 adults and 9 children) were randomized (2:2) between two treatment arms. Treatment arm A began with 12 months of PA, and treatment arm B began with 12 months of IRT. After a 3-month bridging period with cotrimoxazole, the treatment was switched to 12 months of IRT and PA, respectively. The efficacy (measured by the incidence of infections) and proportion of related adverse events in the two arms were compared. RESULTS: The overall efficacy of the two regimens did not differ (p = 0.58, two-sided Wilcoxon signed-rank test). A smaller proportion of patients suffered a related adverse event while using PA (26.8% vs. 60.3%, p < 0.0003, chi-squared test). Patients with persistent infections while using PA suffered fewer infections per year after switching to IRT (2.63 vs. 0.64, p < 0.01). CONCLUSION: We found comparable efficacy of IRT and PA in patients with IgSD ± SPAD. Patients with persistent infections during treatment with PA had less infections after switching to IRT. CLINICAL IMPLICATION: Given the costs and associated side-effects of IRT, it should be reserved for patients with persistent infections despite treatment with PA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10875-020-00841-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7858555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-78585552021-02-11 Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency Smits, Bas M. Kleine Budde, Ilona de Vries, Esther ten Berge, Ineke J. M. Bredius, Robbert G. M. van Deuren, Marcel van Dissel, Jaap T. Ellerbroek, Pauline M. van der Flier, Michiel van Hagen, P. Martin Nieuwhof, Chris Rutgers, Bram Sanders, Lieke E. A. M. Simon, Anna Kuijpers, Taco W. van Montfrans, Joris M. J Clin Immunol Original Article BACKGROUND: Patients with an IgG subclass deficiency (IgSD) ± specific polysaccharide antibody deficiency (SPAD) often present with recurrent infections. Previous retrospective studies have shown that prophylactic antibiotics (PA) and immunoglobulin replacement therapy (IRT) can both be effective in preventing these infections; however, this has not been confirmed in a prospective study. OBJECTIVE: To compare the efficacy of PA and IRT in a randomized crossover trial. METHODS: A total of 64 patients (55 adults and 9 children) were randomized (2:2) between two treatment arms. Treatment arm A began with 12 months of PA, and treatment arm B began with 12 months of IRT. After a 3-month bridging period with cotrimoxazole, the treatment was switched to 12 months of IRT and PA, respectively. The efficacy (measured by the incidence of infections) and proportion of related adverse events in the two arms were compared. RESULTS: The overall efficacy of the two regimens did not differ (p = 0.58, two-sided Wilcoxon signed-rank test). A smaller proportion of patients suffered a related adverse event while using PA (26.8% vs. 60.3%, p < 0.0003, chi-squared test). Patients with persistent infections while using PA suffered fewer infections per year after switching to IRT (2.63 vs. 0.64, p < 0.01). CONCLUSION: We found comparable efficacy of IRT and PA in patients with IgSD ± SPAD. Patients with persistent infections during treatment with PA had less infections after switching to IRT. CLINICAL IMPLICATION: Given the costs and associated side-effects of IRT, it should be reserved for patients with persistent infections despite treatment with PA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10875-020-00841-3) contains supplementary material, which is available to authorized users. Springer US 2020-11-18 2021 /pmc/articles/PMC7858555/ /pubmed/33206257 http://dx.doi.org/10.1007/s10875-020-00841-3 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Smits, Bas M. Kleine Budde, Ilona de Vries, Esther ten Berge, Ineke J. M. Bredius, Robbert G. M. van Deuren, Marcel van Dissel, Jaap T. Ellerbroek, Pauline M. van der Flier, Michiel van Hagen, P. Martin Nieuwhof, Chris Rutgers, Bram Sanders, Lieke E. A. M. Simon, Anna Kuijpers, Taco W. van Montfrans, Joris M. Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency |
title | Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency |
title_full | Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency |
title_fullStr | Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency |
title_full_unstemmed | Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency |
title_short | Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency |
title_sort | immunoglobulin replacement therapy versus antibiotic prophylaxis as treatment for incomplete primary antibody deficiency |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858555/ https://www.ncbi.nlm.nih.gov/pubmed/33206257 http://dx.doi.org/10.1007/s10875-020-00841-3 |
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