Kipar A, Baumgärtner W, Kremmer E, Frese K, Weiss E
Institut für Veterinär-Pathologie, Universität Leipzig, Germany.
Vet Immunol Immunopathol. 1998 Mar 18;62(1):1-13. doi: 10.1016/s0165-2427(97)00170-0.
Forty five cases of canine cutaneous histiocytoma (CCH) were examined by immunohistology for expression and distribution of major histocompatibility complex (MHC) class II antigen in neoplastic cells. In addition, expression of lysozyme and calprotectin (leucocyte protein L1) in neoplastic cells was investigated. Furthermore, B and T lymphocytes were demonstrated by antibodies against the CD3 antigen, IgG, and IgM. Neoplastic cells showed two staining patterns for MHC class II antigen: focal juxtanuclear cytoplasmic staining and/or rim-like staining along the cell periphery. In 24 cases, a predominant or exclusive focal juxtanuclear cytoplasmic MHC class II antigen reaction in neoplastic cells, and the presence of few diffusely distributed infiltrating CD3 antigen-positive T lymphocytes were observed. Tumors with numerous neoplastic cells exhibiting staining for MHC class II antigen along the cell periphery (n = 21) showed increased inflammatory alterations, represented by disseminated and nodular infiltrations of mainly CD3 antigen-positive T cells. B cells, plasma cells, exudate macrophages, and neutrophils were rarely seen disseminated between neoplastic cells whereas their number increased within focal inflammatory infiltrates. The focal cytoplasmic reaction for MHC class II antigen in neoplastic cells might represent newly synthesized MHC class II molecules stored in vesicles, whereas staining of the cell periphery might occur due to accumulation of MHC class II molecules along the plasma membrane. The increasing expression of MHC class II molecules on the cell surface might be the decisive factor for onset and progression of tumor regression. However, the exact mechanism of priming and activation of T cells by neoplastic cells and the nature of the presented antigen are not yet known.
对45例犬皮肤组织细胞瘤(CCH)进行免疫组织学检查,以检测肿瘤细胞中主要组织相容性复合体(MHC)II类抗原的表达和分布。此外,还研究了肿瘤细胞中溶菌酶和钙卫蛋白(白细胞蛋白L1)的表达。此外,用抗CD3抗原、IgG和IgM的抗体证实了B淋巴细胞和T淋巴细胞。肿瘤细胞对MHC II类抗原表现出两种染色模式:局灶性近核周胞质染色和/或沿细胞周边的边缘样染色。在24例病例中,观察到肿瘤细胞中主要为局灶性近核周胞质MHC II类抗原反应,且有少量弥漫性分布的浸润性CD3抗原阳性T淋巴细胞。许多肿瘤细胞沿细胞周边呈现MHC II类抗原染色的肿瘤(n = 21)显示炎症改变增加,主要表现为主要为CD3抗原阳性T细胞的弥漫性和结节性浸润。B细胞、浆细胞、渗出性巨噬细胞和中性粒细胞很少在肿瘤细胞之间弥漫性出现,而它们的数量在局灶性炎症浸润中增加。肿瘤细胞中MHC II类抗原的局灶性胞质反应可能代表储存在囊泡中的新合成的MHC II类分子,而细胞周边的染色可能是由于MHC II类分子沿质膜积累所致。肿瘤细胞表面MHC II类分子表达的增加可能是肿瘤消退发生和进展的决定性因素。然而,肿瘤细胞引发和激活T细胞的确切机制以及所呈递抗原的性质尚不清楚。