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author Davies, E. Graham
Cheung, Melissa
Gilmour, Kimberly
Maimaris, Jesmeen
Curry, Joe
Furmanski, Anna
Sebire, Neil
Halliday, Neil
Mengrelis, Konstantinos
Adams, Stuart
Bernatoniene, Jolanta
Bremner, Ronald
Browning, Michael
Devlin, Blythe
Erichsen, Hans Christian
Gaspar, H. Bobby
Hutchison, Lizzie
Ip, Winnie
Ifversen, Marianne
Leahy, T. Ronan
McCarthy, Elizabeth
Moshous, Despina
Neuling, Kim
Pac, Malgorzata
Papadopol, Alina
Parsley, Kathryn L.
Poliani, Luigi
Ricciardelli, Ida
Sansom, David M.
Voor, Tiia
Worth, Austen
Crompton, Tessa
Markert, M. Louise
Thrasher, Adrian J.
author_facet Davies, E. Graham
Cheung, Melissa
Gilmour, Kimberly
Maimaris, Jesmeen
Curry, Joe
Furmanski, Anna
Sebire, Neil
Halliday, Neil
Mengrelis, Konstantinos
Adams, Stuart
Bernatoniene, Jolanta
Bremner, Ronald
Browning, Michael
Devlin, Blythe
Erichsen, Hans Christian
Gaspar, H. Bobby
Hutchison, Lizzie
Ip, Winnie
Ifversen, Marianne
Leahy, T. Ronan
McCarthy, Elizabeth
Moshous, Despina
Neuling, Kim
Pac, Malgorzata
Papadopol, Alina
Parsley, Kathryn L.
Poliani, Luigi
Ricciardelli, Ida
Sansom, David M.
Voor, Tiia
Worth, Austen
Crompton, Tessa
Markert, M. Louise
Thrasher, Adrian J.
author_sort Davies, E. Graham
collection PubMed
description BACKGROUND: Thymus transplantation is a promising strategy for the treatment of athymic complete DiGeorge syndrome (cDGS). METHODS: Twelve patients with cDGS underwent transplantation with allogeneic cultured thymus. OBJECTIVE: We sought to confirm and extend the results previously obtained in a single center. RESULTS: Two patients died of pre-existing viral infections without having thymopoiesis, and 1 late death occurred from autoimmune thrombocytopenia. One infant had septic shock shortly after transplantation, resulting in graft loss and the need for a second transplant. Evidence of thymopoiesis developed from 5 to 6 months after transplantation in 10 patients. Median circulating naive CD4 counts were 44 × 10(6)/L (range, 11-440 × 10(6)/L) and 200 × 10(6)/L (range, 5-310 × 10(6)/L) at 12 and 24 months after transplantation and T-cell receptor excision circles were 2,238/10(6) T cells (range, 320-8,807/10(6) T cells) and 4,184/10(6) T cells (range, 1,582-24,596/10(6) T cells). Counts did not usually reach normal levels for age, but patients were able to clear pre-existing infections and those acquired later. At a median of 49 months (range, 22-80 months), 8 have ceased prophylactic antimicrobials, and 5 have ceased immunoglobulin replacement. Histologic confirmation of thymopoiesis was seen in 7 of 11 patients undergoing biopsy of transplanted tissue, including 5 showing full maturation through to the terminal stage of Hassall body formation. Autoimmune regulator expression was also demonstrated. Autoimmune complications were seen in 7 of 12 patients. In 2 patients early transient autoimmune hemolysis settled after treatment and did not recur. The other 5 experienced ongoing autoimmune problems, including thyroiditis (3), hemolysis (1), thrombocytopenia (4), and neutropenia (1). CONCLUSIONS: This study confirms the previous reports that thymus transplantation can reconstitute T cells in patients with cDGS but with frequent autoimmune complications in survivors.
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spelling pubmed-57166702017-12-11 Thymus transplantation for complete DiGeorge syndrome: European experience Davies, E. Graham Cheung, Melissa Gilmour, Kimberly Maimaris, Jesmeen Curry, Joe Furmanski, Anna Sebire, Neil Halliday, Neil Mengrelis, Konstantinos Adams, Stuart Bernatoniene, Jolanta Bremner, Ronald Browning, Michael Devlin, Blythe Erichsen, Hans Christian Gaspar, H. Bobby Hutchison, Lizzie Ip, Winnie Ifversen, Marianne Leahy, T. Ronan McCarthy, Elizabeth Moshous, Despina Neuling, Kim Pac, Malgorzata Papadopol, Alina Parsley, Kathryn L. Poliani, Luigi Ricciardelli, Ida Sansom, David M. Voor, Tiia Worth, Austen Crompton, Tessa Markert, M. Louise Thrasher, Adrian J. J Allergy Clin Immunol Article BACKGROUND: Thymus transplantation is a promising strategy for the treatment of athymic complete DiGeorge syndrome (cDGS). METHODS: Twelve patients with cDGS underwent transplantation with allogeneic cultured thymus. OBJECTIVE: We sought to confirm and extend the results previously obtained in a single center. RESULTS: Two patients died of pre-existing viral infections without having thymopoiesis, and 1 late death occurred from autoimmune thrombocytopenia. One infant had septic shock shortly after transplantation, resulting in graft loss and the need for a second transplant. Evidence of thymopoiesis developed from 5 to 6 months after transplantation in 10 patients. Median circulating naive CD4 counts were 44 × 10(6)/L (range, 11-440 × 10(6)/L) and 200 × 10(6)/L (range, 5-310 × 10(6)/L) at 12 and 24 months after transplantation and T-cell receptor excision circles were 2,238/10(6) T cells (range, 320-8,807/10(6) T cells) and 4,184/10(6) T cells (range, 1,582-24,596/10(6) T cells). Counts did not usually reach normal levels for age, but patients were able to clear pre-existing infections and those acquired later. At a median of 49 months (range, 22-80 months), 8 have ceased prophylactic antimicrobials, and 5 have ceased immunoglobulin replacement. Histologic confirmation of thymopoiesis was seen in 7 of 11 patients undergoing biopsy of transplanted tissue, including 5 showing full maturation through to the terminal stage of Hassall body formation. Autoimmune regulator expression was also demonstrated. Autoimmune complications were seen in 7 of 12 patients. In 2 patients early transient autoimmune hemolysis settled after treatment and did not recur. The other 5 experienced ongoing autoimmune problems, including thyroiditis (3), hemolysis (1), thrombocytopenia (4), and neutropenia (1). CONCLUSIONS: This study confirms the previous reports that thymus transplantation can reconstitute T cells in patients with cDGS but with frequent autoimmune complications in survivors. The Authors. Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology. 2017-12 2017-04-08 /pmc/articles/PMC5716670/ /pubmed/28400115 http://dx.doi.org/10.1016/j.jaci.2017.03.020 Text en © 2017 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Davies, E. Graham
Cheung, Melissa
Gilmour, Kimberly
Maimaris, Jesmeen
Curry, Joe
Furmanski, Anna
Sebire, Neil
Halliday, Neil
Mengrelis, Konstantinos
Adams, Stuart
Bernatoniene, Jolanta
Bremner, Ronald
Browning, Michael
Devlin, Blythe
Erichsen, Hans Christian
Gaspar, H. Bobby
Hutchison, Lizzie
Ip, Winnie
Ifversen, Marianne
Leahy, T. Ronan
McCarthy, Elizabeth
Moshous, Despina
Neuling, Kim
Pac, Malgorzata
Papadopol, Alina
Parsley, Kathryn L.
Poliani, Luigi
Ricciardelli, Ida
Sansom, David M.
Voor, Tiia
Worth, Austen
Crompton, Tessa
Markert, M. Louise
Thrasher, Adrian J.
Thymus transplantation for complete DiGeorge syndrome: European experience
title Thymus transplantation for complete DiGeorge syndrome: European experience
title_full Thymus transplantation for complete DiGeorge syndrome: European experience
title_fullStr Thymus transplantation for complete DiGeorge syndrome: European experience
title_full_unstemmed Thymus transplantation for complete DiGeorge syndrome: European experience
title_short Thymus transplantation for complete DiGeorge syndrome: European experience
title_sort thymus transplantation for complete digeorge syndrome: european experience
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716670/
https://www.ncbi.nlm.nih.gov/pubmed/28400115
http://dx.doi.org/10.1016/j.jaci.2017.03.020
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