Departamento de Patologia e Clinicas, Escola de Medicina Veterinaria- Universidade Federal da Bahia, Salvador, Bahia, Brasil.
BMC Cancer. 2010 Jun 4;10:256. doi: 10.1186/1471-2407-10-256.
The immune system plays an important role in the multifactorial biologic system during the development of neoplasias. However, the involvement of the inflammatory response in the promotion/control of malignant cells is still controversial, and the cell subsets and the mechanisms involved are poorly investigated. The goal of this study was to characterize the clinical-pathological status and the immunophenotyping profile of tumor infiltrating lymphocytes and their association with the animal survival rates in canine mammary carcinomas.
Fifty-one animals with mammary carcinomas, classified as carcinomas in mixed tumors-MC-BMT = 31 and carcinomas-MC = 20 were submitted to systematic clinical-pathological analysis (tumor size; presence of lymph node and pulmonary metastasis; clinical stage; histological grade; inflammatory distribution and intensity as well as the lymphocytic infiltrate intensity) and survival rates. Twenty-four animals (MC-BMT = 16 and MC = 8) were elected to the immunophenotypic study performed by flow cytometry.
Data analysis demonstrated that clinical stage II-IV and histological grade was I more frequent in MC-BMT as compared to MC. Univariate analysis demonstrated that the intensity of inflammation (moderate/intense) and the proportion of CD4+ (> or = 66.7%) or CD8+ T-cells (<33.3%) were not associated with worse survival rate. Multivariate analysis demonstrated that only lymphocytic infiltrate intensity > or = 600 (P = 0.02) remained as independent prognostic factor. Despite the clinical manifestation, the lymphocytes represented the predominant cell type in the tumor infiltrate. The percentage of T-cells was higher in animals with MC-BMT without metastasis, while the percentage of B-lymphocytes was greater in animals with metastasized MC-BMT (P < 0.05). The relative percentage of CD4+ T-cells was significantly greater in metastasized tumors (both MC-BMT and MC), (P < 0.05) while the proportion of CD8+ T-cells was higher in MC-BMT without metastasis. Consequently, the CD4+/CD8+ ratio was significantly increased in both groups with metastasis. Regardless of the tumor type, the animals with high proportions of CD4+ and low CD8+ T-cells had decreased survival rates.
The intensity of lymphocytic infiltrate and probably the relative abundance of the CD4+ and CD8+ T-lymphocytes may represent important survival prognostic biomarkers for canine mammary carcinomas.
免疫系统在肿瘤发生的多因素生物系统中起着重要作用。然而,炎症反应在促进/控制恶性细胞中的作用仍存在争议,而且涉及的细胞亚群和机制研究甚少。本研究的目的是描述肿瘤浸润淋巴细胞的临床病理状态和免疫表型特征,并探讨其与犬乳腺肿瘤动物生存率的关系。
对 51 例乳腺肿瘤动物(混合瘤中的癌-MC-BMT=31 例,癌-MC=20 例)进行系统的临床病理分析(肿瘤大小、淋巴结和肺转移的存在、临床分期、组织学分级、炎症分布和强度以及淋巴细胞浸润强度)和生存率分析。选择 24 只动物(MC-BMT=16 只,MC=8 只)进行流式细胞术免疫表型研究。
数据分析表明,MC-BMT 比 MC 更常见临床分期 II-IV 级和组织学分级 I 级。单因素分析表明,炎症强度(中度/重度)和 CD4+(≥66.7%)或 CD8+T 细胞(<33.3%)的比例与生存率较差无关。多因素分析表明,只有淋巴细胞浸润强度>或=600(P=0.02)仍然是独立的预后因素。尽管临床表现不同,但淋巴细胞是肿瘤浸润的主要细胞类型。无转移的 MC-BMT 动物的 T 细胞百分比较高,而有转移的 MC-BMT 动物的 B 淋巴细胞百分比较高(P<0.05)。转移瘤(MC-BMT 和 MC)中 CD4+T 细胞的相对百分比显著增加(P<0.05),而无转移的 MC-BMT 中 CD8+T 细胞的比例较高。因此,两组转移瘤的 CD4+/CD8+比值均显著升高。无论肿瘤类型如何,高比例 CD4+和低比例 CD8+T 细胞的动物生存率降低。
淋巴细胞浸润的强度以及 CD4+和 CD8+T 淋巴细胞的相对丰度可能是犬乳腺肿瘤重要的生存预后生物标志物。