[Combined immunological and cytochemical identification of nucleated cells in normal human peripheral blood].

A Alario, A L Claudy, M Faure, J Thivolet
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Abstract

Nucleated cells obtained from normal human peripheral blood on a layer of Ficoll Isopaque are identified according to the combination of various assays: phagocytosis, endogenous peroxidase, naphtol AS-D esterase, immunofluorescence (IF) performed at 4 degrees C and after incubation at 37 degrees C. The Ig bearing lymphocytes are evaluated with IF, while errors due to other nucleated cells may be evaluated by phagocytic and enzymatic capacities. As the presence of immunoglobulins (Ig) on the cell surface doses not prove its B lymphocytic nature, both immunofluorescence (IF) and endogenous peroxidase are usefully performed together. Exposure of the cells to 37 degrees C during half an hour may enable us to avoid to consider monocytes and lymphocytes with cell bound Ig. Thus con accurately be evaluated the percentages of lymphocytic populations in practice of immunological tests.

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正常人外周血有核细胞的免疫学和细胞化学联合鉴定。
从正常人外周血中获得的有核细胞在Ficoll Isopaque层上进行鉴定,根据多种检测方法的组合进行鉴定:吞噬、内源性过氧化物酶、萘酚AS-D酯酶、免疫荧光(IF),在4℃和37℃孵卵后进行。携带Ig的淋巴细胞用IF评估,而其他有核细胞的错误可能通过吞噬和酶促能力来评估。由于免疫球蛋白(Ig)在细胞表面的存在剂量不能证明其B淋巴细胞性质,因此免疫荧光(IF)和内源性过氧化物酶可以同时进行。将细胞暴露于37℃半小时可使我们避免考虑单核细胞和淋巴细胞结合Ig。因此,在实际的免疫试验中,可以准确地评估淋巴细胞群体的百分比。
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