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Chemotherapy for a secondary malignancy nearly restores complete chimerism in an SCID-patient after HSCT.
Maier, Felix I; Schulz, Ansgar; Furlan, Ingrid; Felgentreff, Kerstin; Jacobsen, Eva-Maria; Sirin, Mehtap; Schwarz, Klaus; Pannicke, Ulrich; Stursberg, Jana; Debatin, Klaus-Michael; Hönig, Manfred.
Afiliação
  • Maier FI; Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Eythstraße 24, 89075 Ulm, Germany. Electronic address: felix.maier@uniklinik-ulm.de.
  • Schulz A; Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Eythstraße 24, 89075 Ulm, Germany.
  • Furlan I; Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Eythstraße 24, 89075 Ulm, Germany.
  • Felgentreff K; Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Eythstraße 24, 89075 Ulm, Germany.
  • Jacobsen EM; Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Eythstraße 24, 89075 Ulm, Germany.
  • Sirin M; Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Eythstraße 24, 89075 Ulm, Germany.
  • Schwarz K; Institute for Transfusion Medicine, University of Ulm, Helmholtzstraße 10, 89081 Ulm, Germany; Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Service Baden-Württemberg-Hessen, Helmholtzstraße 10, 89081 Ulm, Germany.
  • Pannicke U; Institute for Transfusion Medicine, University of Ulm, Helmholtzstraße 10, 89081 Ulm, Germany.
  • Stursberg J; Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Eythstraße 24, 89075 Ulm, Germany.
  • Debatin KM; Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Eythstraße 24, 89075 Ulm, Germany.
  • Hönig M; Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Eythstraße 24, 89075 Ulm, Germany.
Clin Immunol ; 259: 109891, 2024 02.
Article em En | MEDLINE | ID: mdl-38185266
ABSTRACT
For patients with inborn errors of immunity (IEI) and other inborn diseases, mixed donor chimerism is a well-accepted outcome of hematopoietic stem cell transplantation (HSCT). Cytoreductive chemotherapy for a secondary malignancy is a potential challenge for the stability of the graft function after HSCT. We report on a boy with X-SCID who developed Ewing sarcoma ten years after HSCT which was successfully treated with cytoreductive chemotherapy, surgery and local radiation. Surprisingly, this treatment had a positive impact on mixed chimerism with an increase of donor-cell proportions from 40% for neutrophils and 75% for non-T-mononuclear cells (MNCs) to >90% for both. T-cell counts remained stable with 100% of donor origin. This is -to our knowledge- the first report on the impact of cytoreductive chemotherapy on post-HSCT mixed chimerism and provides an important first impression for future patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro / Neoplasias Limite: Humans / Male Idioma: En Revista: Clin Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro / Neoplasias Limite: Humans / Male Idioma: En Revista: Clin Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2024 Tipo de documento: Article