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1000 Titel
  • Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency
1000 Autor/in
  1. Raedler, Johannes |
  2. Magg, Thomas |
  3. Rohlfs, Meino |
  4. Klein, Christoph |
  5. Vallée, Tanja |
  6. Hauck, Fabian |
  7. Albert, Michael |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-06-02
1000 Erschienen in
1000 Quellenangabe
  • 41(7):1536-1548
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s10875-021-01069-5 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452590/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Bi-allelic variants in the dedicator of cytokinesis 8 (DOCK8) gene cause a combined immunodeficiency, characterized by recurrent sinopulmonary and skin infections, food allergies, eczema, eosinophilia, and elevated IgE. Long-term outcome is poor given susceptibility to infections, malignancy, and vascular complications. Allogeneic hematopoietic stem cell transplantation is currently the only curative treatment option and has shown promising outcome. The impact of mixed chimerism on long-term outcome is unclear. We reasoned that reversal of disease phenotype would depend on cell lineage-specific chimerism. DOCK8 variants were confirmed by Sanger and/or exome sequencing and immunoblot and/or intracellular flow cytometry. Donor chimerism was analyzed by XY-fluorescence in situ hybridization or quantitative short tandem repeat PCR. Outcome was assessed by laboratory tests, lymphocyte subsets, intracellular DOCK8 protein flow cytometry, T-cell proliferation analysis, and multiparameter immunoblot allergy screening. We report on nine patients, four of whom with mixed chimerism, with a median follow-up of 78 months after transplantation. Overall, we report successful transplantation with improvement of susceptibility to infections and allergies, and resolution of eczema in all patients. Immunological outcome in patients with mixed chimerism suggests a selective advantage for wild-type donor T-cells but lower donor B-cell chimerism possibly results in a tendency to hypogammaglobulinemia. No increased infectious and allergic complications were associated with mixed chimerism. Aware of the relatively small cohort size, we could not demonstrate a consistent detrimental effect of mixed chimerism on clinical outcomes. We nevertheless advocate aiming for complete donor chimerism in treating DOCK8 deficiency, but recommend reduced toxicity conditioning.
1000 Sacherschließung
lokal Immunologic Deficiency Syndromes/genetics [MeSH]
lokal Mixed chimerism
lokal Virus Diseases/therapy [MeSH]
lokal Guanine Nucleotide Exchange Factors/deficiency [MeSH]
lokal Hypersensitivity/genetics [MeSH]
lokal Original Article
lokal DOCK8 deficiency
lokal Infant [MeSH]
lokal Male [MeSH]
lokal Hypersensitivity/immunology [MeSH]
lokal Immunologic Deficiency Syndromes/therapy [MeSH]
lokal Guanine Nucleotide Exchange Factors/genetics [MeSH]
lokal Child [MeSH]
lokal Immunoglobulin E/blood [MeSH]
lokal Adolescent [MeSH]
lokal Female [MeSH]
lokal Hypersensitivity/therapy [MeSH]
lokal Immunologic Deficiency Syndromes/immunology [MeSH]
lokal Lymphocyte Count [MeSH]
lokal Humans [MeSH]
lokal HSCT
lokal Hematopoietic Stem Cell Transplantation [MeSH]
lokal Retrospective Studies [MeSH]
lokal Virus Diseases/genetics [MeSH]
lokal Virus Diseases/immunology [MeSH]
lokal Chimerism [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/UmFlZGxlciwgSm9oYW5uZXM=|https://frl.publisso.de/adhoc/uri/TWFnZywgVGhvbWFz|https://frl.publisso.de/adhoc/uri/Um9obGZzLCBNZWlubw==|https://frl.publisso.de/adhoc/uri/S2xlaW4sIENocmlzdG9waA==|https://frl.publisso.de/adhoc/uri/VmFsbMOpZSwgVGFuamE=|https://frl.publisso.de/adhoc/uri/SGF1Y2ssIEZhYmlhbg==|https://orcid.org/0000-0001-9143-3263
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1000 Erstellt am 2023-04-28T12:01:31.970+0200
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1000 Zuletzt bearbeitet 2023-10-20T17:27:01.964+0200
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