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可溶性物质诱导的特异性肿瘤免疫:免疫保护的抗原剂量范围和攻击肿瘤负荷范围受限。

Specific tumor immunity induced with soluble materials: restricted range of antigen dose and of challenge tumor load for immunoprotection.

作者信息

Pellis N R, Kahan B D

出版信息

J Immunol. 1975 Dec;115(6):1717-22.

PMID:52676
Abstract

Immunogenic materials were solubilized from two methylcholanthrene-induced fibrosarcomas using 3 M KCl and were assessed for antigen activity in an immunoprotection assay. Mice which had been pretreated with a single injection of extract (0.1 to 2.0 mg protein) were challenged 10 days later with 10(3), 10(4), or 10(5) tumor cells. Optimal protection, as evidenced by survival, tumor incidence, and prolonged latent period before neoplastic outgrowth, was found after pretreatment with 0.5 mg of crude KCl extract and challenge with 10(4) tumor cells. These results further reinforce the weak nature of tumor-specific antigens as immunogens and show that only in very restricted circumstances can solubilized preparations administered without adjuvant induce immunoprotection in syngeneic hosts.

摘要

使用3M氯化钾从两个甲基胆蒽诱导的纤维肉瘤中溶解免疫原性物质,并在免疫保护试验中评估其抗原活性。预先单次注射提取物(0.1至2.0毫克蛋白质)的小鼠在10天后接受10³、10⁴或10⁵个肿瘤细胞的攻击。在用0.5毫克粗氯化钾提取物预处理并接受10⁴个肿瘤细胞攻击后,观察到了最佳保护效果,这体现在生存率、肿瘤发生率以及肿瘤生长前潜伏期延长等方面。这些结果进一步证实了肿瘤特异性抗原作为免疫原的微弱性质,并表明只有在非常有限的情况下,无佐剂给药的溶解制剂才能在同基因宿主中诱导免疫保护。

相似文献

1
Specific tumor immunity induced with soluble materials: restricted range of antigen dose and of challenge tumor load for immunoprotection.可溶性物质诱导的特异性肿瘤免疫:免疫保护的抗原剂量范围和攻击肿瘤负荷范围受限。
J Immunol. 1975 Dec;115(6):1717-22.
2
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J Immunol. 1980 Oct;125(4):1639-43.
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Investigations into the nature of Igh-V region-restricted T cell interactions by using antibodies to antigens on methylcholanthrene-induced sarcomas. I. Analysis of an Igh-V-restricted suppressor-inducer factor.利用针对甲基胆蒽诱导肉瘤上抗原的抗体对Igh-V区限制性T细胞相互作用的性质进行研究。I. Igh-V限制性抑制诱导因子的分析。
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Induction of tumor-specific in vivo protective immunity by immunization with tumor antigen-pulsed antigen-presenting cells.用肿瘤抗原脉冲刺激的抗原呈递细胞进行免疫接种诱导肿瘤特异性体内保护性免疫。
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Cell-mediated immune responses to syngeneic tumors. I. Identification of two distinct CTL effector pathways which differ in antigen specificity, genetic regulation, and cell surface phenotype.对同基因肿瘤的细胞介导免疫反应。I. 两种不同CTL效应途径的鉴定,这两种途径在抗原特异性、遗传调控和细胞表面表型方面存在差异。
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Protective immunity to progressive tumors can be induced by antigen presented on regressor tumors.消退期肿瘤所呈递的抗原可诱导对进行性肿瘤的保护性免疫。
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引用本文的文献

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Susceptibility to the biological effects of polyaromatic hydrocarbons is influenced by genes of the major histocompatibility complex.对多环芳烃生物效应的易感性受主要组织相容性复合体基因的影响。
Proc Natl Acad Sci U S A. 1998 Dec 8;95(25):14915-9. doi: 10.1073/pnas.95.25.14915.
2
Induction of syngeneic tumour-specific immunity by liposomes reconstituted with L2C tumour-cell antigens.用L2C肿瘤细胞抗原重构的脂质体诱导同基因肿瘤特异性免疫。
Immunology. 1983 Jul;49(3):431-8.
3
Immunogenicity of cellular and acellular antigen preparations from a methylcholanthrene-induced mouse sarcoma.
来自甲基胆蒽诱导的小鼠肉瘤的细胞和脱细胞抗原制剂的免疫原性。
J Cancer Res Clin Oncol. 1982;104(3):237-47. doi: 10.1007/BF00406244.
4
Production of a tumor-specific xenoantiserum from partially purified immunoprotective tumor antigen.由部分纯化的免疫保护性肿瘤抗原制备肿瘤特异性异种抗血清。
Cancer Immunol Immunother. 1982;13(1):48-52. doi: 10.1007/BF00200200.
5
Assignment of the gene encoding for Meth A tumour rejection antigen (TATA) to chromosome 12 of the mouse.将编码Meth A肿瘤排斥抗原(TATA)的基因定位到小鼠的12号染色体上。
Br J Cancer. 1984 Jul;50(1):109-11. doi: 10.1038/bjc.1984.145.
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Purification of immunoprotective tumor antigens by preparative isotachophoresis.通过制备型等速电泳纯化免疫保护性肿瘤抗原。
Cancer Immunol Immunother. 1983;16(2):101-8. doi: 10.1007/BF00199240.
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Antibody response to a solubilized tumor-associated membrane antigen (TAMA) from the murine Lewis lung tumor.对来自小鼠Lewis肺癌的可溶性肿瘤相关膜抗原(TAMA)的抗体反应。
Cancer Immunol Immunother. 1983;15(2):131-7. doi: 10.1007/BF00199704.
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Cancer Immunol Immunother. 1985;19(1):22-7. doi: 10.1007/BF00199307.
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