Bone marrow transplantation for T−B− severe combined immunodeficiency disease in Athabascan-speaking native Americans (original) (raw)

Severe Combined Immunodeficiency

Bone Marrow Transplantation volume 27, pages 703–709 (2001)Cite this article

Abstract

A distinct form of autosomal recessive T−B− severe combined immunodeficiency disease occurs with a high frequency among Athabascan-speaking Native Americans (SCIDA), including Navajo and Apache Indians from the southwestern US and Dene Indians from the Canadian Northwest Territories. The SCIDA gene has been linked to markers on chromosome 10p although its identity and role in the pathogenesis of this disease are unknown. We report our experience in treating 18 Navajo and Dene children with SCIDA between 1984 and 1999; 16 underwent bone marrow transplants (BMT). All children were symptomatic within 2 months of birth, had the T−B−NK+SCID phenotype and 67% presented with oral and/or genital ulcers. Three children had evidence of maternal engraftment prior to transplant. Two children died shortly after diagnosis. Three children required more than one BMT and 12 are alive with T cell reconstitution at a median follow-up of 7 years. Three children developed normal B cell immunity, two of whom received ablative conditioning therapy with either radiation or busulfan. Three of the four children who died received therapy with either radiation or busulfan and two of eight long-term survivors who were also recipients of cytotoxic chemotherapy have failed to develop secondary teeth. These results demonstrate the efficacy of BMT in treating infants with this distinct form of SCID, although B cell reconstitution remains a problem even with HLA-matched donors. Without conditioning, T cell engraftment is likely when closely HLA-matched donors are used. With T cell depletion of haplocompatible marrow, conditioning with immunosuppressive therapy may be necessary; however, children with SCIDA who were treated with intensive immunosuppressive and myeloablative therapy had a poor outcome. Bone Marrow Transplantation (2001) 27, 703–709.

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Acknowledgements

We would like to thank the physicians on the Navajo, and Dene reservations for the prompt diagnosis of SCID, the nurses and housestaff at UCSF for the care that these children received pre- and post BMT, and Helen Crouch for her administrative skills in facilitating the transfer of the patients to UCSF and coordinating their evaluations. This work was supported by grants NIH AI28339 and March of Dimes FY95–0954 and FY00-301.

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Author notes

  1. AS O'Marcaigh
    Present address: Hematology Department, Our Lady's Hospital for Sick Children, Dublin, Ireland
  2. K DeSantes
    Present address: Department of Pediatrics, University of Wisconsin, Madison, WI, USA

Authors and Affiliations

  1. Department of Pediatrics Bone Marrow Transplant Division, University of California, San Francisco, CA, USA
    AS O'Marcaigh, K DeSantes, B Horn, L Li & MJ Cowan
  2. Department of Pediatrics, Tuba City Indian Health Services, Tuba City, AZ, USA
    D Hu
  3. Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada
    H Pabst

Authors

  1. AS O'Marcaigh
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  2. K DeSantes
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  3. D Hu
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  4. H Pabst
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  5. B Horn
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  6. L Li
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  7. MJ Cowan
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O'Marcaigh, A., DeSantes, K., Hu, D. et al. Bone marrow transplantation for T−B− severe combined immunodeficiency disease in Athabascan-speaking native Americans.Bone Marrow Transplant 27, 703–709 (2001). https://doi.org/10.1038/sj.bmt.1702831

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