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Successful hematopoietic stem-cell transplantation in a patient with chronic granulomatous disease and McLeod phenotype sensitized to Kx and K antigens

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References

  1. Roos D, Kuijpers T, Curnutte J . Chronic granulomatous disease. In: Ochs H, Smith E, Puck J (eds). Primary Immunodeficiency Diseases, 2nd edn. Oxford University Press: Oxford, New York, 2007, pp 525–549.

    Google Scholar 

  2. Lee S, Russo D, Redman CM . The Kell blood group system: Kell and XK membrane proteins. Semin Hematol 2000; 37: 113–121.

    Article  PubMed  Google Scholar 

  3. Brzica Jr SM, Pineda AA, Taswell HF, Rhodes KH . Chronic granulomatous disease and the McLeod phenotype. Successful treatment of infection with granulocyte transfusions resulting in subsequent hemolytic transfusion reaction. Mayo Clin Proc 1977; 52: 153–156.

    PubMed  Google Scholar 

  4. van der Hart M, Szaloky A, van Loghem JJ . A ‘new’ antibody associated with the Kell blood group system. Vox Sang 1968; 15: 456–458.

    Article  CAS  PubMed  Google Scholar 

  5. Bansal I, Jeon HR, Hui SR, Calhoun BW, Manning DW, Kelly TJ et al. Transfusion support for a patient with McLeod phenotype without chronic granulomatous disease and with antibodies to Kx and Km. Vox Sang 2008; 94: 216–220.

    Article  CAS  PubMed  Google Scholar 

  6. Pu JJ, Redman CM, Visser JW, Lee S . Onset of expression of the components of the Kell blood group complex. Transfusion 2005; 45: 969–974.

    Article  CAS  PubMed  Google Scholar 

  7. Wagner T, Berer A, Lanzer G, Geissler K . Kell is not restricted to the erythropoietic lineage but is also expressed on myeloid progenitor cells. Br J Haematol 2000; 110: 409–411.

    Article  CAS  PubMed  Google Scholar 

  8. Suzuki N, Hatakeyama N, Yamamoto M, Mizue N, Kuroiwa Y, Yoda M et al. Treatment of McLeod phenotype chronic granulomatous disease with reduced-intensity conditioning and unrelated-donor umbilical cord blood transplantation. Int J Hematol 2007; 85: 70–72.

    Article  PubMed  Google Scholar 

  9. Kordes U, Binder TMC, Eiermann TH, Hassenpflug-Diederich B, Hassan MA, Beutel K et al. Successful donor-lymphocyte infusion for extreme immune-hemolysis following unrelated BMT in a patient with X-linked chronic granulomatous disease and McLeod phenotype. Bone Marrow Transplant 2008; 42: 219–220.

    Article  CAS  PubMed  Google Scholar 

  10. Franchini M, Gandini G, Aprili G . Non-ABO red blood cell alloantibodies following allogeneic hematopoietic stem cell transplantation. Bone Marrow Transplant 2004; 33: 1169.

    Article  CAS  PubMed  Google Scholar 

  11. Kent WJ, Sugnet CW, Furey TS, Roskin KM, Pringle TH, Zahler AM et al. The human genome browser at UCSC. Genome Res 2002; 12: 996–1006.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Correspondence to W Friedrich.

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Hönig, M., Flegel, W., Schwarz, K. et al. Successful hematopoietic stem-cell transplantation in a patient with chronic granulomatous disease and McLeod phenotype sensitized to Kx and K antigens. Bone Marrow Transplant 45, 209–211 (2010). https://doi.org/10.1038/bmt.2009.115

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