Efficacy of the Antigenicity-Retaining Ability of Fixative Solutions for Liquid-Based Cytology: Immunocytochemistry of Long-Term Storage

被引:4
|
作者
Sato, Hiaki [1 ]
Norimatsu, Yoshiaki [2 ]
Irino, Satoshi [3 ]
Nishikawa, Takeshi [4 ]
机构
[1] Hokuriku Univ, Fac Hlth & Med Sci, Dept Med Technol & Clin Engn, Kanazawa, Ishikawa, Japan
[2] Ehime Prefectural Univ Hlth Sci, Fac Hlth Sci, Dept Med Technol, Tobe, Japan
[3] Ehime Prefectural Univ Hlth Sci, Dept Nursing, Tobe, Japan
[4] Nara Med Univ Hosp, Dept Pathol, Nara, Japan
关键词
Antigenicity-retaining ability; Fixative solution; Liquid-based cytology; Immunocytochemical staining; Long-term storage; FORMALIN TISSUE FIXATION; CERVICAL-CANCER; P53; IMMUNOREACTIVITY; EXPRESSION; ANTIBODIES; PROTEINS; MUTATION; DNA;
D O I
10.1159/000518452
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Introduction/Objective: Liquid-based cytology (LBC) is advantageous as multiple stained specimens can be prepared and used for additional assays such as immunocytochemical and molecular-pathological investigations. Two types of preservative-fixative solutions (fixatives) are used for nongynecologic specimens used in the BD SurePath-LBC (SP-LBC) method, and their components vary. However, few studies have evaluated the differences in antigen-retaining ability between these fixatives. Therefore, we investigated and compared the antigen-retaining ability of the fixatives in immunocytochemical staining (ICC) under long-term storage conditions. Materials and Methods: Sediments of cultured RAJI cells (derived from Burkitt's lymphoma) were added to each fixative (red and blue) and stored at room temperature for a specified period (1 h; 1 week; and 1, 3, and 6 months). The specimens were then prepared using the SP-LBC method and subjected to ICC. Positivity rate was calculated using the specimens fixed at room temperature for 1 h as a control. Antibodies against Ki67 expressed in the nucleus and against CD20 and leukocyte common antigen (LCA) expressed on the cell membrane were used. Results: For CD20 and LCA, the positivity rate increased with time in the red fixative compared with that in the control. In the blue fixative, the positivity rate was highest at 1 h and was maintained at a high level throughout the storage period. In contrast, the Ki67 positivity rate was highest at 1 h in both red and blue fixatives and markedly decreased with time. Therefore, although refrigerated (8 degrees C) storage was used, no improvement was noted. Conclusions: Long-term storage is possible for cell membrane antigens at room temperature; however, it is unsuitable for intranuclear antigens. Therefore, we conclude that suitable fixative type and storage temperature differ based on antigen location. Further investigation is warranted.
引用
收藏
页码:510 / 521
页数:12
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