Banks P M, Caron B L, Morgan T W
Am J Clin Pathol. 1983 Apr;79(4):438-42. doi: 10.1093/ajcp/79.4.438.
Air-dried imprint preparations are conveniently produced from human lymphoid samples without the special methods required for snap-freezing tissues or rendering them into suspensions. T-cells, T-cell subsets (helper and suppressor), and HLA-DR-positive cells (B-lymphocytes, monocytic-histiocytic cells) can be identified in such imprints by the use of commercially obtained mouse hybridoma antibodies with a simple two-step immunoperoxidase method. Direct nuclear morphologic correlation with surface determinants is achieved by this method. Immunoreactivity is retained only eight to 10 days in such air-dried preparations, and attempts to prolong reactivity have been unsuccessful so far.
空气干燥印片标本可方便地从人淋巴样样本制备,无需速冻组织或将其制成悬液所需的特殊方法。通过使用市售小鼠杂交瘤抗体,采用简单的两步免疫过氧化物酶法,可在此类印片中识别T细胞、T细胞亚群(辅助性和抑制性)以及HLA-DR阳性细胞(B淋巴细胞、单核-组织细胞)。该方法可实现细胞核形态与表面决定簇的直接关联。在此类空气干燥标本中,免疫反应性仅保留8至10天,迄今为止延长反应性的尝试均未成功。