Wang B L, Springer G F, Kaufman M W
Heather M. Bligh Cancer Research Laboratories, Chicago Medical School, IL 60064, USA.
J Histochem Cytochem. 1996 Feb;44(2):187-91. doi: 10.1177/44.2.8609376.
The composition of tumor-infiltrating lymphocytes (TIL) often reflects the host's immune response to the tumor. To study the relationship of TIL and carcinoma-associated T/Tn antigens in breast carcinoma, a straightforward concurrent immunoenzyme staining procedure was developed. Fresh tissue was directly fixed in a zinc-based fixative to preserve lymphocyte markers and then routinely embedded in paraffin. The TIL subtypes in the sections were identified in the first immunostaining cycle by reaction with a monoclonal antibody (MAb) to lymphocyte markers CD3, CD4, CD8, CD19, or CD56, followed by a modified avidin-biotin procedure and diaminobenzidine tetrahydrochloride-H2O2 for color development. This was followed by paraformaldehyde fixation to block antibody crossreactivity. The T and Tn antigens on carcinoma cells were then demonstrated in a second staining cycle by reaction with an MAb against T or Tn antigen, followed by an indirect immunoalkaline phosphatase procedure and corresponding substrate systems for color development. The distinguishable brown color for TIL and blue or red color for T or Tn antigen enabled us to identify the TIL subsets and to describe their relations with T/Tn antigen expression in situ. This approach may contribute to better understanding of the patients' immune defenses against their tumor and aid in prognostication.
肿瘤浸润淋巴细胞(TIL)的组成常常反映宿主对肿瘤的免疫反应。为了研究乳腺癌中TIL与癌相关T/Tn抗原的关系,开发了一种直接的同步免疫酶染色方法。新鲜组织直接固定于锌基固定剂中以保存淋巴细胞标志物,然后常规石蜡包埋。在第一个免疫染色循环中,通过与针对淋巴细胞标志物CD3、CD4、CD8、CD19或CD56的单克隆抗体(MAb)反应来识别切片中的TIL亚型,随后采用改良的抗生物素蛋白-生物素方法和四盐酸二氨基联苯胺-H2O2进行显色。接着用多聚甲醛固定以阻断抗体交叉反应。然后在第二个染色循环中,通过与抗T或Tn抗原的MAb反应来显示癌细胞上的T和Tn抗原,随后采用间接免疫碱性磷酸酶方法和相应的底物系统进行显色。TIL呈现可区分的棕色,T或Tn抗原呈现蓝色或红色,这使我们能够原位识别TIL亚群并描述它们与T/Tn抗原表达的关系。这种方法可能有助于更好地理解患者针对肿瘤的免疫防御,并有助于预后判断。