Sarcoidosis Following Hematopoietic Stem Cell Transplantation: Clinical Characteristics and HLA Associations.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2021
Historique:
received: 25 07 2021
accepted: 20 09 2021
entrez: 25 10 2021
pubmed: 26 10 2021
medline: 17 12 2021
Statut: epublish

Résumé

Extrinsic factors and genetic predisposition contribute to the etiology of sarcoidosis, converging in a phenotype of altered immune response associated with multisystemic inflammatory granulomatous tissue infiltration. Immunological reconstitution after hematopoietic stem cell transplantation (HSCT) may represent a unique window for the pathogenesis of the disease. We describe the incidence, clinicopathological features, and HLA associations of sarcoidosis after HSCT in a single-center cohort of patients, together with data from previously published cases. We retrospectively analyzed clinical characteristics and HLA haplotypes from allogeneic (allo) or autologous (auto) HSCT patients from January 2001 through May 2021 at the University Medicine Goettingen (UMG), and data from previously published cases. A total number of 19 patients was identified. These included 4 patients from our center (3 allo HSCT and 1 auto HSCT) and 15 patients from the literature review. Thirteen patients had received an allo HSCT, and six patients had received an auto HSCT. Sarcoidosis occurred after a median interval of 20 (after allo HSCT) and 7 (after auto HSCT) months, respectively. The predominant HLA allele associated with sarcoidosis was HLA DRB1*03:01. Sarcoidosis involved the respiratory tract in 15 patients (three unknown, one without pulmonary involvement), and it was associated with graft-versus-host disease in 7 of 13 patients receiving allo HSCT. None of the donors or patients had a history of sarcoidosis before transplantation. Disease manifestations resolved with standard glucocorticoid treatment without long-term sequelae. Sarcoidosis may occur at low frequency during reconstitution of the immune system after HSCT. HLA allele associations reflect the associations observed in the general population, particularly with DRB1*03:01. Further insights into the interplay between Tcell reconstitution and the development of sarcoidosis could also provide novel approaches to an improved understanding of the pathogenesis in sarcoidosis.

Identifiants

pubmed: 34691055
doi: 10.3389/fimmu.2021.746996
pmc: PMC8529157
doi:

Substances chimiques

HLA Antigens 0

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

746996

Informations de copyright

Copyright © 2021 Wurm-Kuczera, Buentzel, Koenig, Legler, Valk, Hasenkamp, Jung, Rademacher, Korsten and Wulf.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Rebecca Isabel Wurm-Kuczera (RI)

Department of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.

Judith Buentzel (J)

Department of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.

Julia Felicitas Leni Koenig (JFL)

Department of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.

Tobias Legler (T)

Department of Transfusion Medicine, University Medical Center Goettingen, Goettingen, Germany.

Jan-Jakob Valk (JJ)

Department of Transfusion Medicine, University Medical Center Goettingen, Goettingen, Germany.

Justin Hasenkamp (J)

Department of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.

Wolfram Jung (W)

Department of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.

Jan-Gerd Rademacher (JG)

Department of Nephrology and Rheumatology, University Medical Center Goettingen, Goettingen, Germany.

Peter Korsten (P)

Department of Nephrology and Rheumatology, University Medical Center Goettingen, Goettingen, Germany.

Gerald Georg Wulf (GG)

Department of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.

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