CNRS-UMR 8080 'Développement et Evolution', Université Paris-Sud, Orsay Cedex, France.
Cell Prolif. 2010 Jun;43(3):326-32. doi: 10.1111/j.1365-2184.2010.00678.x.
To elucidate the natural history of T-cell large granular lymphocyte (T-LGL) lymphoproliferation, we followed changes in associated fluctuating neutropenia for 3 years in an untreated patient presenting with the disease.
We report a nonlinear mathematical analysis of irregular neutrophil fluctuation, using iterative data maps, to detect long-term regulation of the neutrophil population.
This geometric analysis indicated that variations of this sequence of neutrophil counts followed bounded deterministic dynamics around a fixed low level equilibrium, a situation similar to that previously observed for cultured mouse early bone marrow progenitor cells.
These findings illustrate how the deleterious effect of T-LGL on neutrophils is balanced, over periods of years, by pulses of compensatory neutrophil production, potentially accounting for the commonly observed prolonged indolent course of the disease.
为了阐明 T 细胞大颗粒淋巴细胞(T-LGL)淋巴增生的自然史,我们对一名未经治疗的患者在 3 年内与疾病相关的波动中性粒细胞减少症的变化进行了随访。
我们报告了一种使用迭代数据图对不规则中性粒细胞波动的非线性数学分析,以检测中性粒细胞群体的长期调节。
这种几何分析表明,该序列中性粒细胞计数的变化遵循固定低水平平衡的有界确定性动力学,这种情况类似于以前观察到的培养的小鼠早期骨髓祖细胞。
这些发现说明了 T-LGL 对中性粒细胞的有害影响是如何在数年的时间内通过补偿性中性粒细胞生成的脉冲来平衡的,这可能解释了疾病通常观察到的迁延性病程。