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Hematopoietic Stem Cell Transplant for the Treatment of X-MAID

We report outcomes after hematopoietic stem cell transplant for three patients with X-MAID, including 1 patient from the originally described cohort and two brothers with positive TREC newborn screening for SCID who were found to have a T-B-NK+ SCID phenotype attributable to X-linked moesin associat...

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Autores principales: Henrickson, Sarah E., Andre-Schmutz, Isabelle, Lagresle-Peyrou, Chantal, Deardorff, Matthew A., Jyonouchi, Harumi, Neven, Benedicte, Bunin, Nancy, Heimall, Jennifer R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527778/
https://www.ncbi.nlm.nih.gov/pubmed/31139601
http://dx.doi.org/10.3389/fped.2019.00170
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author Henrickson, Sarah E.
Andre-Schmutz, Isabelle
Lagresle-Peyrou, Chantal
Deardorff, Matthew A.
Jyonouchi, Harumi
Neven, Benedicte
Bunin, Nancy
Heimall, Jennifer R.
author_facet Henrickson, Sarah E.
Andre-Schmutz, Isabelle
Lagresle-Peyrou, Chantal
Deardorff, Matthew A.
Jyonouchi, Harumi
Neven, Benedicte
Bunin, Nancy
Heimall, Jennifer R.
author_sort Henrickson, Sarah E.
collection PubMed
description We report outcomes after hematopoietic stem cell transplant for three patients with X-MAID, including 1 patient from the originally described cohort and two brothers with positive TREC newborn screening for SCID who were found to have a T-B-NK+ SCID phenotype attributable to X-linked moesin associated immunodeficiency (X-MAID). A c.511C>T variant in moesin was identified via exome sequencing in the older of these siblings in the setting of low lymphocyte counts and poor proliferative responses consistent with SCID. He received reduced intensity conditioning due to CMV, and was transplanted with a T-depleted haploidentical (maternal) donor. His post-transplant course was complicated by hemolytic anemia, neutropenia, and sepsis. He had poor engraftment, requiring a 2nd transplant. His younger brother presented with the same clinical phenotype and was treated with umbilical cord blood transplant following myeloablative conditioning, has engrafted and is doing well. The third case also presented with severe lymphopenia in infancy, received a matched related bone marrow transplant following myeloablative conditioning, has engrafted and is doing well. These cases represent a novel manifestation of non-radiosensitive X-linked form of T-B-NK+ SCID that is able to be detected by TREC based newborn screening and effectively treated with HCT.
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spelling pubmed-65277782019-05-28 Hematopoietic Stem Cell Transplant for the Treatment of X-MAID Henrickson, Sarah E. Andre-Schmutz, Isabelle Lagresle-Peyrou, Chantal Deardorff, Matthew A. Jyonouchi, Harumi Neven, Benedicte Bunin, Nancy Heimall, Jennifer R. Front Pediatr Pediatrics We report outcomes after hematopoietic stem cell transplant for three patients with X-MAID, including 1 patient from the originally described cohort and two brothers with positive TREC newborn screening for SCID who were found to have a T-B-NK+ SCID phenotype attributable to X-linked moesin associated immunodeficiency (X-MAID). A c.511C>T variant in moesin was identified via exome sequencing in the older of these siblings in the setting of low lymphocyte counts and poor proliferative responses consistent with SCID. He received reduced intensity conditioning due to CMV, and was transplanted with a T-depleted haploidentical (maternal) donor. His post-transplant course was complicated by hemolytic anemia, neutropenia, and sepsis. He had poor engraftment, requiring a 2nd transplant. His younger brother presented with the same clinical phenotype and was treated with umbilical cord blood transplant following myeloablative conditioning, has engrafted and is doing well. The third case also presented with severe lymphopenia in infancy, received a matched related bone marrow transplant following myeloablative conditioning, has engrafted and is doing well. These cases represent a novel manifestation of non-radiosensitive X-linked form of T-B-NK+ SCID that is able to be detected by TREC based newborn screening and effectively treated with HCT. Frontiers Media S.A. 2019-05-14 /pmc/articles/PMC6527778/ /pubmed/31139601 http://dx.doi.org/10.3389/fped.2019.00170 Text en Copyright © 2019 Henrickson, Andre-Schmutz, Lagresle-Peyrou, Deardorff, Jyonouchi, Neven, Bunin and Heimall. 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 Pediatrics
Henrickson, Sarah E.
Andre-Schmutz, Isabelle
Lagresle-Peyrou, Chantal
Deardorff, Matthew A.
Jyonouchi, Harumi
Neven, Benedicte
Bunin, Nancy
Heimall, Jennifer R.
Hematopoietic Stem Cell Transplant for the Treatment of X-MAID
title Hematopoietic Stem Cell Transplant for the Treatment of X-MAID
title_full Hematopoietic Stem Cell Transplant for the Treatment of X-MAID
title_fullStr Hematopoietic Stem Cell Transplant for the Treatment of X-MAID
title_full_unstemmed Hematopoietic Stem Cell Transplant for the Treatment of X-MAID
title_short Hematopoietic Stem Cell Transplant for the Treatment of X-MAID
title_sort hematopoietic stem cell transplant for the treatment of x-maid
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527778/
https://www.ncbi.nlm.nih.gov/pubmed/31139601
http://dx.doi.org/10.3389/fped.2019.00170
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