Mulligan S P, Wills E J, Young G A
Clinical Immunology Research Centre, University of Sydney, N.S.W., Australia.
Br J Haematol. 1990 Jun;75(2):175-80. doi: 10.1111/j.1365-2141.1990.tb02645.x.
This report describes a patient with a large granular lymphocyte leukaemia (CD8 + lymphoproliferative disease) and severe neutropenia (less than 0.5 x 10(9)/l) in whom exercise resulted in a marked lymphocytosis, a phenomenon which has not previously been recorded. The lymphocyte count at rest was within normal limits (2.2 x 10(9)/l), then fell to the resting level within 15 min of cessation of exercise. The peripheral blood mononuclear cells showed the morphology of large granular lymphocytes (LGL) by light and electron microscopy both at rest (30%) and to a much greater extent during exercise (70%). Immunophenotyping of these lymphocytes during exercise demonstrated that the predominant cell was CD3+, CD8+, CD57+ (Leu7)/CD4-, CD16-, CD25-. In the resting state, despite a total lymphocyte count within the normal range, surface marker studies indicated an excess of cells with the CD8+/CD57 + T cell phenotype (26%; cf. normal range less than or equal to 10%). Functional assays revealed a minimal increase in natural killer (NK) activity during exercise. T cell receptor beta chain gene rearrangement was demonstrable in the peripheral blood at rest and during exercise. Although severe neutropenia was present, the growth of normal colony forming units, granulocyte-macrophage (CFU-GM) was not inhibited by patient lymphocytes and no anti-neutrophil antibodies were demonstrated. Finally, hyposplenism has developed and the relationship of this to the LGL leukaemia is discussed. In summary, the findings demonstrated large granular lymphocyte leukaemia as the primary disorder for which the primary manifestation, apart from the neutropenia, was a marked exercise-induced lymphocytosis.
本报告描述了一名患有大颗粒淋巴细胞白血病(CD8 + 淋巴细胞增殖性疾病)和严重中性粒细胞减少症(低于0.5×10⁹/L)的患者,其运动后出现显著的淋巴细胞增多,这一现象此前未见记录。静息时淋巴细胞计数在正常范围内(2.2×10⁹/L),运动停止后15分钟内降至静息水平。外周血单个核细胞在静息时(30%)以及运动期间(70%,程度更高)通过光镜和电镜均显示出大颗粒淋巴细胞(LGL)的形态。运动期间这些淋巴细胞的免疫表型分析表明,主要细胞为CD3⁺、CD8⁺、CD57⁺(Leu7)/CD4⁻、CD16⁻、CD25⁻。在静息状态下,尽管总淋巴细胞计数在正常范围内,但表面标志物研究表明具有CD8⁺/CD57⁺ T细胞表型的细胞过量(26%;正常范围≤10%)。功能测定显示运动期间自然杀伤(NK)活性仅有轻微增加。静息时和运动期间外周血中均可检测到T细胞受体β链基因重排。尽管存在严重中性粒细胞减少症,但患者淋巴细胞并未抑制正常集落形成单位、粒细胞 - 巨噬细胞(CFU - GM)的生长,且未检测到抗中性粒细胞抗体。最后,患者出现了脾功能减退,并讨论了其与LGL白血病的关系。总之,研究结果表明大颗粒淋巴细胞白血病是主要疾病,除中性粒细胞减少症外,其主要表现为运动诱导的显著淋巴细胞增多。