Fitzgerald M G
J Clin Pathol. 1972 Feb;25(2):163-8. doi: 10.1136/jcp.25.2.163.
Despite widespread doubts about the quantitative validity or clinical usefulness of lymphocyte response to phytohaemagglutinin (PHA), a satisfactory quantitative test of such responsiveness suitable for the clinical recognition of immunological defects has been developed here. This was achieved by exploring and controlling technical and other variables in the culture of lymphocytes and the quantitation of their response to phytohaemagglutinin. The aspects evaluated included intraperson as well as person-to-person variations, non-lymphocytic cell content, lymphocyte number, PHA batch, atmospheric conditions, culture duration, and quantitation of response. As a result of the information gained from these studies, together with the normal dose-response curve previously established (Fitzgerald, 1971), a satisfactory quantitative and reproducible method suitable for routine clinical use has been realized. This has been applied to the investigation of patients with suspected immunological deficiency disorders, and significant deviations from the normal have been shown. In addition, a PHA dose-response ratio derived from the responses of normal individuals and patients gives a practical quantitative expression of such defects.
尽管对于淋巴细胞对植物血凝素(PHA)反应的定量有效性或临床实用性存在广泛质疑,但本文已开发出一种适用于临床识别免疫缺陷的此类反应性的令人满意的定量检测方法。这是通过探索和控制淋巴细胞培养中的技术及其他变量以及对其对植物血凝素反应的定量来实现的。评估的方面包括个体内以及个体间的差异、非淋巴细胞含量、淋巴细胞数量、PHA批次、大气条件、培养持续时间以及反应的定量。从这些研究中获得的信息,连同先前建立的正常剂量反应曲线(菲茨杰拉德,1971年),实现了一种适用于常规临床使用的令人满意的定量且可重复的方法。这已应用于对疑似免疫缺陷疾病患者的调查,并显示出与正常情况的显著偏差。此外,由正常个体和患者的反应得出的PHA剂量反应比给出了此类缺陷的实际定量表达。