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Immunohistological characterisation of tumour infiltrating lymphocytes in melanocytic skin lesions.

机译:黑色素细胞皮肤病变中肿瘤浸润淋巴细胞的免疫组织学表征。

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BACKGROUND: Although the presence of tumour infiltrating lymphocytes (TIL) is a constant feature in melanomas, their immunophenotypic characterisation is still incomplete. We hypothesise that the transition from normal skin to benign naevi (BN) to melanocytic dysplastic naevi (MDN) to radial growth phase cutaneous malignant melanoma (RGP-CMM) to vertical growth phase cutaneous malignant melanoma (VGP-CMM) is associated with alterations in TIL. This study attempted to test this hypothesis and to characterise TIL in the melanocytic skin lesions. METHODS: In total, 74 lesions (12 BN, 12 MDN, 13 RGP-CMM, 26 VGP-CMM, and 11 metastatic melanomas) were examined using immunoperoxidase staining methods and antibodies targeting leukocyte common antigen (LCA+), T (CD3+) and B (CD20+) lymphocytes, and resting cytotoxic T cells (TIA-1+). RESULTS: Histologically, the transitions from normal skin to BN to MDN to RGP-CMM to VGP-CMM was associated with a gradual increase in the numbers of TIL (total, parenchymal, stromal, perivascular, and epidermal TIL, as well as TIL at the base of the lesions). The numbers of TIL were higher at the stroma than at the parenchyma. Similarly, immunostaining revealed that these transitions were associated with a gradual increase in the staining values (staining intensity, percentage of positive cells, and immunoreactivity score) for LCA+, CD20+, CD3+, and TIA-1+cells. The number of CD3+ cells was higher than that of CD20+ cells. All these differences between the normal skin and the lesional ones reached statistical significance (p<0.01). The majority of CD3+ cells were TIA-1+ T cells with cytotoxic potential. Compared with primary melanomas, there was a decrease in TIL in metastatic melanomas. CONCLUSIONS: The gradual increase in TIL during melanoma tumorigenesis may reflect increased antigenicity of the tumour cells. Although both humoral and cell mediated immunity are involved in melanomagenesis, the latter seems to have the major role. The immune profile of MDN suggests their intermediacy between BN and CMM.
机译:背景:尽管黑色素瘤中肿瘤浸润淋巴细胞(TIL)的存在是一个恒定的特征,但其免疫表型特征仍然不完整。我们假设从正常皮肤到良性痣(BN)到黑素细胞增生异常痣(MDN)到放射状生长期皮肤恶性黑色素瘤(RGP-CMM)到垂直生长期皮肤恶性黑色素瘤(VGP-CMM)的转变瓷砖。这项研究试图检验这一假设并表征黑素细胞性皮肤病变中的TIL。方法:使用免疫过氧化物酶染色法和针对白细胞共同抗原(LCA +),T(CD3 +)和T细胞的抗体,共检查了74个病变(12 BN,12 MDN,13 RGP-CMM,26 VGP-CMM和11个转移性黑色素瘤)。 B(CD20 +)淋巴细胞和静止的细胞毒性T细胞(TIA-1 +)。结果:从组织学上看,从正常皮肤到BN到MDN到RGP-CMM到VGP-CMM的转变与TIL(总,实质,间质,血管周围和表皮TIL的数量)逐渐增加有关病变的基础)。 TIL的数量在基质处高于实质。同样,免疫染色显示,这些转变与LCA +,CD20 +,CD3 +和TIA-1 +细胞的染色值(染色强度,阳性细胞百分比和免疫反应评分)的逐渐增加有关。 CD3 +细胞的数量高于CD20 +细胞的数量。正常皮肤和病变皮肤之间的所有这些差异均达到统计学意义(p <0.01)。大多数CD3 +细胞是具有细胞毒性潜能的TIA-1 + T细胞。与原发性黑色素瘤相比,转移性黑色素瘤的TIL降低。结论:黑色素瘤发生过程中TIL的逐渐增加可能反映了肿瘤细胞的抗原性增加。尽管体液免疫和细胞介导的免疫均参与黑色素瘤的发生,但后者似乎起主要作用。 MDN的免疫特征表明它们在BN和CMM之间具有中介作用。

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