Hiratsuka H, Imamura M, Ishii Y, Kohama G, Kikuchi K
Cancer. 1984 Jun 1;53(11):2456-66. doi: 10.1002/1097-0142(19840601)53:11<2456::aid-cncr2820531116>3.0.co;2-6.
Cancer tissues from 30 patients with squamous cell carcinoma of the oral cavity were examined immunohistopathologically as to the responsiveness of the host against its own cancer cells in both biopsy and surgically resected specimens from the same patients. Subpopulations of the infiltrating lymphocytes in cancer tissues were identified on paraffin-embedded serial sections by a modified indirect immunoperoxidase technique (PAB method) in which it was combined with peroxidase-antiperoxidase (PAP) complex and avidin-biotin system with rabbit anti-human B-cell, peripheral T-cell sera. Macrophages were also identified by nonspecific acid esterase staining. T-cells were predominant over B-cells in 26 of 30 tissues in biopsy specimens and 23 of 30 in surgically resected specimens with bleomycin treatment. T-cell infiltration in the peripheral region of the tumor was more prominent than that in the stroma among the cancer nests. T-cells surrounded the cancer nests, occasionally accumulated around the cancer cells, infiltrated at the marginal part of the cancer nests, and frequently produced perivascular massive accumulations. B-cells and macrophages, on the other hand, were almost absent or negligible around cancer tissues. The grade of T-cell infiltration, especially in biopsied specimens, was correlated well to the size of the tumor, and also more marked significantly in patients without cervical lymph node metastasis than in those with lymph node metastasis. Furthermore, there was a significant correlation between the grade of T-cell infiltration at the peripheral region of the invading cancer mass in initial biopsy specimens and the clinical tumor regression rates with bleomycin treatment, but it did not correlate to the surgically resected specimens. These facts suggest that T-cells might inhibit the development and spreading of the cancer cells, and that the T-cell infiltration correlates with the clinical course or prognosis of the oral cancer patients.
对30例口腔鳞状细胞癌患者的癌组织进行了免疫组织病理学检查,以研究同一患者活检标本和手术切除标本中宿主对自身癌细胞的反应性。采用改良间接免疫过氧化物酶技术(PAB法),将其与过氧化物酶 - 抗过氧化物酶(PAP)复合物及抗生物素蛋白 - 生物素系统相结合,并使用兔抗人B细胞、外周血T细胞血清,在石蜡包埋的连续切片上识别癌组织中浸润淋巴细胞的亚群。巨噬细胞也通过非特异性酸性酯酶染色进行识别。在活检标本的30个组织中有26个以及接受博来霉素治疗的手术切除标本的30个中有23个,T细胞比B细胞占优势。肿瘤外周区域的T细胞浸润比癌巢间基质中的更明显。T细胞围绕癌巢,偶尔在癌细胞周围聚集,在癌巢边缘浸润,并经常在血管周围大量聚集。另一方面,癌组织周围几乎没有B细胞和巨噬细胞,或数量可忽略不计。T细胞浸润程度,尤其是活检标本中的,与肿瘤大小密切相关,并且在无颈部淋巴结转移的患者中比有淋巴结转移的患者更显著。此外,初始活检标本中侵袭性癌块外周区域的T细胞浸润程度与博来霉素治疗后的临床肿瘤消退率之间存在显著相关性,但与手术切除标本无关。这些事实表明,T细胞可能抑制癌细胞的发展和扩散,并且T细胞浸润与口腔癌患者的临床病程或预后相关。