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细胞因子基因修饰的自体肿瘤细胞疫苗接种诱导的针对黑色素瘤抗原的体液免疫反应。

Humoral immune response against melanoma antigens induced by vaccination with cytokine gene-modified autologous tumor cells.

作者信息

Ehlken Hanno, Schadendorf Dirk, Eichmüller Stefan

机构信息

German Cancer Research Center (DKFZ), Skin Cancer Unit (D070), Heidelberg, Germany.

出版信息

Int J Cancer. 2004 Jan 10;108(2):307-13. doi: 10.1002/ijc.11537.

DOI:10.1002/ijc.11537
PMID:14639620
Abstract

Although the existence of a humoral response against tumor-associated antigens is well appreciated, a systematic analysis of its possible induction by the tumor remains missing. We compared the specific IgG response of Stage IV melanoma patients during vaccination. Patients had been treated within 2 clinical trials with autologous tumor cells gene-modified for IL-7 or IL-12. A panel of 27 tumor-associated antigens (HD-MM-01 to HD-MM-27) was isolated by a SEREX screening of a testis cDNA library using a pool of 5 sera from patients after vaccination. All antigens were retested with individual sera of 12 patients both pre- and post-vaccination. A serological response was induced during vaccination against 18 antigens. Remarkably, induction was detected only in patients included in the screening pool. The low overlap between sero-reactivity of the 12 patients suggested a very individualized immunological reaction. Two of 5 sera included in the screening pool exhibited a high frequency of induced humoral responses. The same patients had been shown to have a high Karnovsky index and had generated lytic cytotoxic T cells against the tumor. Besides 2 known cancer-germline genes (SCP-1 and PLU-1), the other isolated antigens were expressed in a non-tumor-specific fashion as analyzed by virtual Northern blot or RT-PCR. The properties of homologues to several of the identified tumor-antigens, especially PLU-1, SCP-1, DNEL2, CLOCK, and PIASx-alpha, suggest further investigation of their possible function in malignant melanoma. We conclude that a strong humoral response against tumor-associated antigens is inducible by tumor cells and that this response is very individual.

摘要

尽管针对肿瘤相关抗原的体液免疫反应的存在已得到充分认识,但对肿瘤可能诱导该反应的系统分析仍缺失。我们比较了IV期黑色素瘤患者在疫苗接种期间的特异性IgG反应。患者在两项临床试验中接受了用IL-7或IL-12基因修饰的自体肿瘤细胞治疗。通过使用接种后患者的5份血清池对睾丸cDNA文库进行SEREX筛选,分离出一组27种肿瘤相关抗原(HD-MM-01至HD-MM-27)。所有抗原均用12名患者接种前和接种后的个体血清重新检测。疫苗接种期间诱导了针对18种抗原的血清学反应。值得注意的是,仅在筛选池中的患者中检测到诱导。12名患者的血清反应性之间的低重叠表明免疫反应非常个体化。筛选池中包含的5份血清中有2份表现出高频率的诱导体液反应。相同的患者已被证明具有高卡诺夫斯基指数,并产生了针对肿瘤的溶细胞性细胞毒性T细胞。除了2个已知的癌胚基因(SCP-1和PLU-1)外,通过虚拟Northern印迹或RT-PCR分析,其他分离的抗原以非肿瘤特异性方式表达。几种已鉴定的肿瘤抗原的同源物的特性,特别是PLU-1、SCP-1、DNEL2、CLOCK和PIASx-α,表明需要进一步研究它们在恶性黑色素瘤中的可能功能。我们得出结论,肿瘤细胞可诱导针对肿瘤相关抗原的强烈体液反应,并且这种反应非常个体化。

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Metastatic melanomas express inhibitory low affinity fc gamma receptor and escape humoral immunity.
转移性黑色素瘤表达抑制性低亲和力Fcγ受体并逃避体液免疫。
Dermatol Res Pract. 2010;2010:657406. doi: 10.1155/2010/657406. Epub 2010 Jun 28.
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