Sitnicka Ewa
Hematopoietic Stem Cell Laboratory, Lund Research Center for Stem Cell Biology and Cell Therapy, Lund University, Lund.
Crit Rev Immunol. 2009;29(6):487-530. doi: 10.1615/critrevimmunol.v29.i6.30.
The thymus produces new T cells throughout life but has no self-renewing ability and requires replenishment and recruitment of progenitors derived from the bone marrow. Despite the progress in delineation of mature blood cell development several questions remain regarding T lymphopoiesis. Understanding the developmental stages from multipotent hematopoietic stem cells (HSCs) to the T-cell lineage-restricted progenitors has many potential clinical implications as it is important for understanding malignant transformation in T-cell cancer, accelerating T-cell regeneration after bone marrow transplantation and chemotherapy, and establishing new therapies to treat T-cell immune deficiencies. This review focuses on the steps leading from the HSCs in the bone marrow to the lineage committed T cells inside the thymus.
胸腺在人的一生中持续产生新的T细胞,但它没有自我更新能力,需要补充和募集源自骨髓的祖细胞。尽管在成熟血细胞发育的描述方面取得了进展,但关于T淋巴细胞生成仍存在一些问题。了解从多能造血干细胞(HSC)到T细胞谱系受限祖细胞的发育阶段具有许多潜在的临床意义,因为这对于理解T细胞癌中的恶性转化、加速骨髓移植和化疗后的T细胞再生以及建立治疗T细胞免疫缺陷的新疗法非常重要。本综述重点关注从骨髓中的造血干细胞到胸腺内谱系定向T细胞的过程。