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Monoclonal antibody treatment during pregnancy and/or lactation in women with MS or neuromyelitis optica spectrum disorder

OBJECTIVE: To assess possible adverse effects on breastfed infants of mothers receiving monoclonal antibodies (MAbs) during pregnancy and/or lactation. METHODS: We identified 23 patients from the German Multiple Sclerosis and Pregnancy Registry (DMSKW) who received MAbs (17 natalizumab and 6 anti-CD...

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Autores principales: Ciplea, Andrea Ines, Langer-Gould, Annette, de Vries, Annick, Schaap, Tiny, Thiel, Sandra, Ringelstein, Marius, Gold, Ralf, Hellwig, Kerstin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188475/
https://www.ncbi.nlm.nih.gov/pubmed/32327455
http://dx.doi.org/10.1212/NXI.0000000000000723
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author Ciplea, Andrea Ines
Langer-Gould, Annette
de Vries, Annick
Schaap, Tiny
Thiel, Sandra
Ringelstein, Marius
Gold, Ralf
Hellwig, Kerstin
author_facet Ciplea, Andrea Ines
Langer-Gould, Annette
de Vries, Annick
Schaap, Tiny
Thiel, Sandra
Ringelstein, Marius
Gold, Ralf
Hellwig, Kerstin
author_sort Ciplea, Andrea Ines
collection PubMed
description OBJECTIVE: To assess possible adverse effects on breastfed infants of mothers receiving monoclonal antibodies (MAbs) during pregnancy and/or lactation. METHODS: We identified 23 patients from the German Multiple Sclerosis and Pregnancy Registry (DMSKW) who received MAbs (17 natalizumab and 6 anti-CD20) during lactation. Thirteen were already exposed to natalizumab during the third trimester of pregnancy, and 1 received ocrelizumab during pregnancy. Data were obtained from standardized, telephone-administered questionnaires completed by the mother during pregnancy and at 1, 3, 6, and 12 months postpartum. Natalizumab concentration in mother’s milk was analyzed in 3 patients and natalizumab serum concentration in 2 of these patients and their breastfed infants. RESULTS: We did not observe a negative impact on infant health and development attributable to breast milk exposure after a median follow-up of 1 year. Infants exposed to natalizumab during the third trimester had a lower birth weight and more hospitalizations in the first year of life. The concentration of natalizumab in breast milk and serum of infants was low; B cells normal in infants breastfed under anti-CD20. CONCLUSION: More data on the effect of Mab exposure during pregnancy are needed. Otherwise, our data suggest that treatment with natalizumab, ocrelizumab, or rituximab during lactation might be safe for breastfed infants.
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spelling pubmed-71884752020-05-04 Monoclonal antibody treatment during pregnancy and/or lactation in women with MS or neuromyelitis optica spectrum disorder Ciplea, Andrea Ines Langer-Gould, Annette de Vries, Annick Schaap, Tiny Thiel, Sandra Ringelstein, Marius Gold, Ralf Hellwig, Kerstin Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To assess possible adverse effects on breastfed infants of mothers receiving monoclonal antibodies (MAbs) during pregnancy and/or lactation. METHODS: We identified 23 patients from the German Multiple Sclerosis and Pregnancy Registry (DMSKW) who received MAbs (17 natalizumab and 6 anti-CD20) during lactation. Thirteen were already exposed to natalizumab during the third trimester of pregnancy, and 1 received ocrelizumab during pregnancy. Data were obtained from standardized, telephone-administered questionnaires completed by the mother during pregnancy and at 1, 3, 6, and 12 months postpartum. Natalizumab concentration in mother’s milk was analyzed in 3 patients and natalizumab serum concentration in 2 of these patients and their breastfed infants. RESULTS: We did not observe a negative impact on infant health and development attributable to breast milk exposure after a median follow-up of 1 year. Infants exposed to natalizumab during the third trimester had a lower birth weight and more hospitalizations in the first year of life. The concentration of natalizumab in breast milk and serum of infants was low; B cells normal in infants breastfed under anti-CD20. CONCLUSION: More data on the effect of Mab exposure during pregnancy are needed. Otherwise, our data suggest that treatment with natalizumab, ocrelizumab, or rituximab during lactation might be safe for breastfed infants. Lippincott Williams & Wilkins 2020-04-23 /pmc/articles/PMC7188475/ /pubmed/32327455 http://dx.doi.org/10.1212/NXI.0000000000000723 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Ciplea, Andrea Ines
Langer-Gould, Annette
de Vries, Annick
Schaap, Tiny
Thiel, Sandra
Ringelstein, Marius
Gold, Ralf
Hellwig, Kerstin
Monoclonal antibody treatment during pregnancy and/or lactation in women with MS or neuromyelitis optica spectrum disorder
title Monoclonal antibody treatment during pregnancy and/or lactation in women with MS or neuromyelitis optica spectrum disorder
title_full Monoclonal antibody treatment during pregnancy and/or lactation in women with MS or neuromyelitis optica spectrum disorder
title_fullStr Monoclonal antibody treatment during pregnancy and/or lactation in women with MS or neuromyelitis optica spectrum disorder
title_full_unstemmed Monoclonal antibody treatment during pregnancy and/or lactation in women with MS or neuromyelitis optica spectrum disorder
title_short Monoclonal antibody treatment during pregnancy and/or lactation in women with MS or neuromyelitis optica spectrum disorder
title_sort monoclonal antibody treatment during pregnancy and/or lactation in women with ms or neuromyelitis optica spectrum disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188475/
https://www.ncbi.nlm.nih.gov/pubmed/32327455
http://dx.doi.org/10.1212/NXI.0000000000000723
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