4.5 Article

Highly skewed T-cell receptor V-beta chain repertoire in the bone marrow is associated with response to immunosuppressive drug therapy in children with very severe aplastic anemia

期刊

BLOOD CANCER JOURNAL
卷 1, 期 -, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/bcj.2011.6

关键词

aplastic anemia; T-cell receptor V-beta chain repertoire; children

资金

  1. Else-Kroner Fresenius Stiftung
  2. European Community
  3. Elterninitiative Kinderkrebsklinik Dusseldorf e.V.
  4. Elterninitative Intern 3 Munchen e.V.
  5. Deutsche Forschungsgemeinschaft [SFB-571-A1]

向作者/读者索取更多资源

One of the major obstacles of immunosuppressive therapy (IST) in children with severe aplastic anemia (SAA) comes from the often months-long unpredictability of bone-marrow (BM) recovery. In this prospective study in children with newly diagnosed very severe AA (n = 10), who were enrolled in the therapy study SAA-BFM 94, we found a dramatically reduced diversity of both CD4+ and CD8+ BM cells, as scored by comprehensive V-beta chain T-cell receptor (TCR) analysis. Strongly skewed TCR V-beta pattern was highly predictive for good or at least partial treatment response (n = 6, CD8+ complexity scoring median 35.5, range 24-73). In contrast, IST in patients with rather moderate reduction of TCR V-beta diversity (n = 4, CD8+ complexity scoring median 109.5, range 82-124) always failed (P = 0.0095). If confirmed in a larger series of patients, TCR V-beta repertoire in BM may help to assign children with SAA up-front either to IST or to allogeneic stem-cell transplantation. Blood Cancer Journal (2011) 1, e8; doi:10.1038/bcj.2011.6; published online 4 March 2011

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