New therapeutic approaches for protecting hematopoietic stem cells in aplastic anemia

Wendy Weston, Vineet Gupta, Rebecca Adkins, Roland Jurecic

Research output: Contribution to journalArticlepeer-review


Aplastic anemia (AA) is an immune-mediated and life-threatening form of acquired bone marrow failure (BMF), characterized by development and expansion of self-reactive T cells these T cells cause continuous destruction of hematopoietic stem cells (HSCs), progenitors, and mature blood cells, leading to severe and if left untreated fatal marrow hypoplasia and pancytopenia. Standard treatment options for patients with AA include: (1) immunosuppressive therapy (IST) with anti-thymocyte globulin and cyclosporine A which targets self-reactive T cells, or (2) matched sibling or unrelated BM transplant (BMT) the IST treatment is often not effective due to poor response to therapy or disease relapse after IST. Also, BMT is not an option for many patients due to their age, comorbidities, and the lack of histocompatible donor. This necessitates development and testing of novel approaches to reduce severity of AA and to efficiently treat patients with refractory and relapsed AA. Immune-mediated AA was reproduced in animals, including mouse lymphocyte infusion models, which are used to study further etiology and pathophysiology of AA and test new drugs and approaches in treating and managing AA. In these mouse models the immune correlates and pathologic features of AA are strikingly similar to features of severe human AA. In this article we (a) briefly review standard and developing approaches for treating AA and (b) describe development and testing of novel treatment approach with a potential to safely reduce BM hypoplasia and significantly decrease the loss of HSCs in mouse lymphocyte infusion model of AA.

Original languageEnglish (US)
Pages (from-to)34-43
Number of pages10
JournalImmunologic Research
Issue number1-3
StatePublished - Dec 2013
Externally publishedYes


  • Aplastic anemia
  • Bone marrow failure
  • Dendritic cells
  • Hematopoietic stem cells
  • Immunosuppressive therapy
  • T cells
  • β2 integrin CD11b/CD18

ASJC Scopus subject areas

  • Immunology


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