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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

机译:骨髓中高度偏斜的T细胞受体V-β链库与非常严重的再生障碍性贫血儿童对免疫抑制药物治疗的反应有关

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摘要

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.
机译:患有严重再生障碍性贫血(SAA)的儿童的免疫抑制疗法(IST)的主要障碍之一,是骨髓(BM)康复通常长达数月之久。在这项针对SAA-BFM 94治疗研究的新诊断为非常严重的AA(n = 10)的儿童的前瞻性研究中,我们发现CD4 +和CD8 + BM细胞的多样性显着降低,由综合V- β链T细胞受体(TCR)分析。强烈偏斜的TCRV-β模式可预测良好或至少部分治疗反应(n = 6,CD8 +复杂性得分中位数35.5,范围24-73)。相反,TCRV-β多样性相当适度降低(n = 4,CD8 +复杂性得分中位数为109.5,范围82-124)的IST总是失败(P = 0.0095)。如果在更多的患者中得到证实,则BM中的TCR V-beta库可能有助于预先将SAA患儿分配给IST或同种异体干细胞移植。

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