Skip to main content
Erschienen in: Journal of Clinical Immunology 5/2021

05.02.2021 | Letter to Editor

Immune Reconstitution after Hematopoietic Stem Cell Transplantation in Immunodeficiency–Centromeric Instability–Facial Anomalies Syndrome Type 1

verfasst von: Monica T. Kraft, Lubna S. Mehyar, Benjamin T. Prince, Shalini C. Reshmi, Roshini S. Abraham, Rolla Abu-Arja

Erschienen in: Journal of Clinical Immunology | Ausgabe 5/2021

Einloggen, um Zugang zu erhalten

Excerpt

To the Editor: …
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Hagleitner MM, Lankester A, Maraschio P, Hultén M, Fryns JP, Schuetz C, et al. Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome). J Med Genet. 2008;45(2):93–9.CrossRef Hagleitner MM, Lankester A, Maraschio P, Hultén M, Fryns JP, Schuetz C, et al. Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome). J Med Genet. 2008;45(2):93–9.CrossRef
3.
Zurück zum Zitat Sterlin D, Velasco G, Moshous D, Touzot F, Mahlaoui N, Fischer A, et al. Genetic, cellular and clinical features of ICF syndrome: a French national survey. J Clin Immunol. 2016;36(2):149–59.CrossRef Sterlin D, Velasco G, Moshous D, Touzot F, Mahlaoui N, Fischer A, et al. Genetic, cellular and clinical features of ICF syndrome: a French national survey. J Clin Immunol. 2016;36(2):149–59.CrossRef
4.
Zurück zum Zitat Weemaes CM, van Tol MJ, Wang J, van Ostaijen-ten Dam MM, van Eggermond MC, Thijssen PE, et al. Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects. Eur J Hum Genet. 2013;21(11):1219–25.CrossRef Weemaes CM, van Tol MJ, Wang J, van Ostaijen-ten Dam MM, van Eggermond MC, Thijssen PE, et al. Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects. Eur J Hum Genet. 2013;21(11):1219–25.CrossRef
5.
Zurück zum Zitat Kamae C, Imai K, Kato T, Okano T, Honma K, Nakagawa N, et al. Clinical and immunological characterization of ICF syndrome in Japan. J Clin Immunol. 2018;38(8):927–37.CrossRef Kamae C, Imai K, Kato T, Okano T, Honma K, Nakagawa N, et al. Clinical and immunological characterization of ICF syndrome in Japan. J Clin Immunol. 2018;38(8):927–37.CrossRef
6.
Zurück zum Zitat Gennery AR, Slatter MA, Bredius RG, Hagleitner MM, Weemaes C, Cant AJ, et al. Hematopoietic stem cell transplantation corrects the immunologic abnormalities associated with immunodeficiency-centromeric instability-facial dysmorphism syndrome. Pediatrics. 2007;120(5):e1341–4.CrossRef Gennery AR, Slatter MA, Bredius RG, Hagleitner MM, Weemaes C, Cant AJ, et al. Hematopoietic stem cell transplantation corrects the immunologic abnormalities associated with immunodeficiency-centromeric instability-facial dysmorphism syndrome. Pediatrics. 2007;120(5):e1341–4.CrossRef
7.
Zurück zum Zitat Kellner ES, Rathbun PA, Marshall GS, Tolusso LK, Smolarek TA, Sun M, et al. The value of chromosome analysis to interrogate variants in DNMT3B causing immunodeficiency, centromeric instability, and facial anomaly syndrome type I (ICF1). J Clin Immunol. 2019;39(8):857–9.CrossRef Kellner ES, Rathbun PA, Marshall GS, Tolusso LK, Smolarek TA, Sun M, et al. The value of chromosome analysis to interrogate variants in DNMT3B causing immunodeficiency, centromeric instability, and facial anomaly syndrome type I (ICF1). J Clin Immunol. 2019;39(8):857–9.CrossRef
9.
Zurück zum Zitat Bacigalupo A, Ballen K, Rizzo D, Giralt S, Lazarus H, Ho V, et al. Defining the intensity of conditioning regimens: working definitions. Biol Blood Marrow Transplant. 2009;15(12):1628–33.CrossRef Bacigalupo A, Ballen K, Rizzo D, Giralt S, Lazarus H, Ho V, et al. Defining the intensity of conditioning regimens: working definitions. Biol Blood Marrow Transplant. 2009;15(12):1628–33.CrossRef
10.
Zurück zum Zitat Connelly JA, Marsh R, Parikh S, Talano J-A. Allogeneic hematopoietic cell transplantation for chronic granulomatous disease: controversies and state of the art. J Pediatr Infect Dis Soc. 2018;7(suppl_1):S31–9.CrossRef Connelly JA, Marsh R, Parikh S, Talano J-A. Allogeneic hematopoietic cell transplantation for chronic granulomatous disease: controversies and state of the art. J Pediatr Infect Dis Soc. 2018;7(suppl_1):S31–9.CrossRef
11.
Zurück zum Zitat Chandra S, Bleesing JJ, Jordan MB, Grimley MS, Khandelwal P, Davies SM, et al. Post-transplant CD34+ selected stem cell “boost” for mixed chimerism after reduced-intensity conditioning hematopoietic stem cell transplantation in children and young adults with primary immune deficiencies. Biol Blood Marrow Transplant. 2018;24(7):1527–9.CrossRef Chandra S, Bleesing JJ, Jordan MB, Grimley MS, Khandelwal P, Davies SM, et al. Post-transplant CD34+ selected stem cell “boost” for mixed chimerism after reduced-intensity conditioning hematopoietic stem cell transplantation in children and young adults with primary immune deficiencies. Biol Blood Marrow Transplant. 2018;24(7):1527–9.CrossRef
12.
Zurück zum Zitat Slatter MA, Rao K, Amrolia P, Flood T, Abinun M, Hambleton S, et al. Treosulfan-based conditioning regimens for hematopoietic stem cell transplantation in children with primary immunodeficiency: United Kingdom experience. Blood. 2011;117(16):4367–75.CrossRef Slatter MA, Rao K, Amrolia P, Flood T, Abinun M, Hambleton S, et al. Treosulfan-based conditioning regimens for hematopoietic stem cell transplantation in children with primary immunodeficiency: United Kingdom experience. Blood. 2011;117(16):4367–75.CrossRef
13.
Zurück zum Zitat Burk CM, Coffey KE, Mace EM, Bostwick BL, Chinn IK, Coban-Akdemir ZH, et al. Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome with NK dysfunction and EBV-driven malignancy treated with stem cell transplantation. J Allergy Clin Immunol Pract. 2020;8(3):1103–1106.e3.CrossRef Burk CM, Coffey KE, Mace EM, Bostwick BL, Chinn IK, Coban-Akdemir ZH, et al. Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome with NK dysfunction and EBV-driven malignancy treated with stem cell transplantation. J Allergy Clin Immunol Pract. 2020;8(3):1103–1106.e3.CrossRef
14.
Zurück zum Zitat Marsh RA, Vaughn G, Kim M-O, Li D, Jodele S, Joshi S, et al. Reduced-intensity conditioning significantly improves survival of patients with hemophagocytic lymphohistiocytosis undergoing allogeneic hematopoietic cell transplantation. Blood. 2010;116(26):5824–31.CrossRef Marsh RA, Vaughn G, Kim M-O, Li D, Jodele S, Joshi S, et al. Reduced-intensity conditioning significantly improves survival of patients with hemophagocytic lymphohistiocytosis undergoing allogeneic hematopoietic cell transplantation. Blood. 2010;116(26):5824–31.CrossRef
Metadaten
Titel
Immune Reconstitution after Hematopoietic Stem Cell Transplantation in Immunodeficiency–Centromeric Instability–Facial Anomalies Syndrome Type 1
verfasst von
Monica T. Kraft
Lubna S. Mehyar
Benjamin T. Prince
Shalini C. Reshmi
Roshini S. Abraham
Rolla Abu-Arja
Publikationsdatum
05.02.2021
Verlag
Springer US
Erschienen in
Journal of Clinical Immunology / Ausgabe 5/2021
Print ISSN: 0271-9142
Elektronische ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-021-00984-x

Weitere Artikel der Ausgabe 5/2021

Journal of Clinical Immunology 5/2021 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.