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Autoimmunity

Rituximab is effective in the management of refractory autoimmune cytopenias occurring after allogeneic stem cell transplantation

Summary:

Autoimmune haemolytic anaemia (AIHA), immune thrombocytopenia (ITP) and autoimmune neutropenia (AIN) are well-recognised complications of allogeneic stem cell transplantation (SCT), but have previously only been reported in the context of myeloablative conditioning regimens. Management of AIHA, ITP or AIN occurring after allogeneic SCT is unsatisfactory since they frequently prove refractory to conventional therapies including splenectomy. As a consequence, autoimmune cytopenias occurring after allogeneic SCT are associated with substantial morbidity and mortality. We report four patients who developed AIHA or ITP after allogeneic transplantation – three of which occurred after a reduced-intensity conditioning (RIC) regimen. All patients demonstrated a complete response to Rituximab, having failed to respond to conventional treatment including high-dose prednisolone and intravenous immunoglobulin (IVIg). We conclude that Rituximab can be a valuable agent in the management of autoimmune cytopenias occurring after allogeneic SCT and that autoimmune cytopenias may be a hitherto unrecognised complication of RIC regimens.

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References

  1. Horn B, Viele M, Mentzer W et al. Autoimmune hemolytic anemia in patients with SCID after T-cell depleted BM and PBSC transplantation. Bone Marrow Transplant 1999; 24: 1009–1013.

    Article  CAS  Google Scholar 

  2. Herbert H, Einsele H, Klien R et al. CMV infection after allogeneic transplantation is associated with the occurrence of various autoantibodies and monoclonal gammopathies. Br J Haematol 1996; 95: 138–144.

    Article  Google Scholar 

  3. Drobyski WR, Potluri J, Sauer D et al. Autoimmune hemolytic anemia following T-cell depleted allogeneic bone marrow transplantation. Bone Marrow Transplant 1996; 17: 1093–1099.

    CAS  Google Scholar 

  4. Cwynarski K, Goulding R, Pocock C et al. Immune hemolytic anemia following T-cell depleted allogeneic bone marrow transplantation for chronic myeloid leukaemia: association with leukaemic relapse and treatment with donor lymphocyte infusions. Bone Marrow Transplant 2001; 28: 581–586.

    Article  CAS  Google Scholar 

  5. Klumpp TR, Herman JH, Schnell M et al. Association between antibodies reactive with neutrophils, rate of neutrophil engraftment, and incidence of post-engraftment neutropenia following BMT. Bone Marrow Transplant 1996; 18: 559–564.

    CAS  PubMed  Google Scholar 

  6. Kottaridis PD, Milligan DW, Chopra R et al. In vivo CAMPATH-1H prevents graft-versus-host disease following nonmyeloablative stem cell transplantation. Blood 2000; 96: 2419–2425.

    CAS  Google Scholar 

  7. Chakraverty R, Peggs K, Chopra R et al. Limiting transplantation-related mortality following unrelated donor stem cell transplantation by using a nonmyeloablative conditioning regimen. Blood 2002; 99: 1071–1078.

    Article  CAS  Google Scholar 

  8. Maris MB, Niederwieser D, Sandmeier BM et al. HLA-matched unrelated donor hematopoietic cell transplantation after nonmyeloablative conditioning for patients with hematologic malignancies. Blood 2003; 102: 2021–2030.

    Article  CAS  Google Scholar 

  9. Faulkner RD, Craddock C, Byrne JL et al. BEAM-alemtuzumab reduced-intensity allogeneic stem cell transplantation for lymphoproliferative diseases: GVHD, toxicity and survival in 65 patients. Blood 2004; 103: 428–434.

    Article  CAS  Google Scholar 

  10. Delgrado J, Bustos JG, Jimenez-Yuste V et al. Anti- CD20 monoclonal antibody in refractory immune thrombocytopenic purpura. Haematologica 2002; 87: 215–216.

    Google Scholar 

  11. Zaja F, Iaocona I, Masolini P et al. B-cell depletion with Rituximab as treatment for immune hemolytic anemia and chronic thrombocytopenia. Haematologica 2002; 87: 189–195.

    CAS  PubMed  Google Scholar 

  12. Stasi R, Pagano A, Stipa E et al. Rituximab chimeric CD20 antibody treatment for adults with chronic idiopathic thrombocytopenic purpura. Blood 2001; 98: 952–957.

    Article  CAS  Google Scholar 

  13. Ratanatharathorn V, Carson E, Reynolds C et al. Anti-CD20 chimeric monoclonal antibody treatment of refractory immune-mediated thrombocytopenia in a patient with chronic graft-versus-host disease. Ann Int Med 2000; 133: 275–279.

    Article  CAS  Google Scholar 

  14. Hongeng S, Tardong P, Worapongpaiboon S . Successful treatment of refractory autoimmune hemolytic anaemia in a post-unrelated bone marrow transplant paediatric patient with Rituximab. Bone Marrow Transplant 2002; 29: 871–872.

    Article  CAS  Google Scholar 

  15. Corti P, Bonanomi S, Vallinoto C et al. Rituximab for immune hemolytic anaemia following T and B cell depleted hematopoietic stem cell transplantation. Acta Haematol 2003; 109: 43–45.

    Article  CAS  Google Scholar 

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Correspondence to C Craddock.

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Raj, K., Narayanan, S., Augustson, B. et al. Rituximab is effective in the management of refractory autoimmune cytopenias occurring after allogeneic stem cell transplantation. Bone Marrow Transplant 35, 299–301 (2005). https://doi.org/10.1038/sj.bmt.1704705

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