Circulating T-cell subpopulations in lithium-associated granulocytosis.

A D Crockard, Z R Desai, K T Ennis
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引用次数: 6

Abstract

Granulocytosis is a common feature in patients undergoing lithium therapy. With increasing evidence that T lymphocytes play a role in the control of granulopoiesis, we have investigated the effect of lithium administration on circulating levels of T helper and T suppressor cells, as identified by monoclonal antibodies, to determine whether lithium-induced granulocytosis is mediated through changes in peripheral blood T cell subsets. Lithium carbonate was administered to 10 subjects over a 2 week period. Differential leucocyte counts and T, B, T helper and T suppressor lymphocyte enumerations were performed prior to administration of lithium (Day 1) and on 2 occasions (Day 7 and 14) during ingestion of the drug. Ten healthy control subjects were similarly investigated. Small, but significant elevation (p less than 0.05) in neutrophil counts at 7 and 14 days were observed in subjects taking lithium, serum lithium levels at these times were 0.56 +/- 0.27 and 0.68 +/- 0.17 mmol/l, respectively; lymphocyte and monocyte levels were unaffected. The percentages and absolute numbers of circulating T, B, T helper and T suppressor lymphocytes were not significantly altered (p greater than 0.05) during lithium administration and did not differ significantly (p greater than 0.05) from those recorded for the control group. We were thus unable to demonstrate that short-term lithium administration induced changes in the circulating levels of T helper (OKT4+) or T suppressor (OKT8+) cells.

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锂相关粒细胞缺乏症的循环t细胞亚群。
粒细胞缺乏症是接受锂离子治疗的患者的共同特征。随着越来越多的证据表明T淋巴细胞在控制粒细胞生成中发挥作用,我们研究了锂给药对循环中T辅助细胞和T抑制细胞水平的影响,通过单克隆抗体鉴定,以确定锂诱导的粒细胞生成是否通过外周血T细胞亚群的变化介导。10名受试者在2周的时间内服用碳酸锂。在给药前(第1天)和服药期间2次(第7天和第14天)进行白细胞计数和T、B、T辅助和T抑制淋巴细胞计数。10名健康对照者也进行了类似的调查。在服用锂的受试者中,中性粒细胞计数在第7天和第14天小幅但显著升高(p < 0.05),这两个时期的血清锂水平分别为0.56 +/- 0.27和0.68 +/- 0.17 mmol/l;淋巴细胞和单核细胞水平未受影响。锂治疗组循环T淋巴细胞、B淋巴细胞、T辅助淋巴细胞和T抑制淋巴细胞的百分比和绝对数量无显著变化(p > 0.05),与对照组相比无显著差异(p > 0.05)。因此,我们无法证明短期锂治疗诱导T辅助细胞(OKT4+)或T抑制细胞(OKT8+)循环水平的变化。
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