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携带甲基胆蒽诱导肉瘤的小鼠的抑制性淋巴结细胞对肿瘤相关抗原的细胞介导细胞毒性的抑制作用。

Inhibition of cell-mediated cytotoxicity against tumor-associated antigens by suppressor lymph node cells from mice bearing methylcholanthrene-induced sarcomas.

作者信息

Indrová M, Bubeník J

出版信息

Neoplasma. 1979;26(4):405-12.

PMID:160510
Abstract

Suppression of cell-mediated cytotoxicity directed against tumor-associated membrane antigens of methylcholanthrene (MC)-induced sarcomas by lymph node cells (LNC) from tumor-bearing mice was examined by inhibition of the 3H-thymidine incorporation assay. Normal LNC from B10 mice had been sensitized in vitro by 6-day cultivation on layers of irradiated syngeneic sarcoma cells and the effect of the generated cytotoxic lymphocytes was then inhibited by the admixture of suppressor cells present in lymph nodes of tumor-bearing mice. Suppressor cells were detected in lymph nodes from 7 of 16 (44 per cent) individually examined tumor bearers when LNC were added to cytotoxic lymphocytes which had been presensitized in vitro. When the experimental schedule was reverted and the tumor bearers' LNC were admixed to the normal LNC prior to the in vitro sensitization so that they were present in the population of the effector cells throughout the period of sensitization, the suppressor effect was detected in only 1 of 9 (11 per cent) tumor-bearers. The suppressive effect of tumor bearers' LNC was found to be nonspecific, being elicited not only by LNC derived from bearers of the sensitizing tumor, but also by LNC from bearers of an unrelated, immunologically noncross-reacting MC-induced sarcoma.

摘要

通过抑制³H-胸腺嘧啶核苷掺入试验,研究了荷瘤小鼠的淋巴结细胞(LNC)对甲基胆蒽(MC)诱导的肉瘤的肿瘤相关膜抗原的细胞介导细胞毒性的抑制作用。来自B10小鼠的正常LNC在体外通过在经照射的同基因肉瘤细胞层上培养6天进行致敏,然后通过荷瘤小鼠淋巴结中存在的抑制细胞的混合来抑制产生的细胞毒性淋巴细胞的作用。当将LNC添加到体外预先致敏的细胞毒性淋巴细胞中时,在16只单独检查的荷瘤小鼠中的7只(44%)的淋巴结中检测到抑制细胞。当实验方案颠倒过来,在体外致敏之前将荷瘤小鼠的LNC与正常LNC混合,以使它们在整个致敏期间存在于效应细胞群体中时,在9只荷瘤小鼠中仅1只(11%)检测到抑制作用。发现荷瘤小鼠的LNC的抑制作用是非特异性的,不仅由致敏肿瘤携带者的LNC引起,也由来自无关的、免疫非交叉反应的MC诱导肉瘤携带者的LNC引起。

相似文献

1
Inhibition of cell-mediated cytotoxicity against tumor-associated antigens by suppressor lymph node cells from mice bearing methylcholanthrene-induced sarcomas.携带甲基胆蒽诱导肉瘤的小鼠的抑制性淋巴结细胞对肿瘤相关抗原的细胞介导细胞毒性的抑制作用。
Neoplasma. 1979;26(4):405-12.
2
Cell-mediated immune reactions as probes of sensitization to tumour-associated antigens of methylcholanthrene-induced mouse sarcomas.细胞介导的免疫反应作为对甲基胆蒽诱导的小鼠肉瘤肿瘤相关抗原致敏的探针。
Arch Geschwulstforsch. 1981;51(4):349-53.
3
Non T suppressor cells in the lymph nodes of mice bearing methylcholanthrene-induced sarcomas.
Folia Biol (Praha). 1981;27(3):217-22.
4
In vitro immunization against tumour-associated antigen of methylcholanthrene-induced sarcoma.甲基胆蒽诱导肉瘤的肿瘤相关抗原的体外免疫
Folia Biol (Praha). 1978;24(2):118-27.
5
Specific stimulatory and cytotoxic effects of lymphocytes sensitized in vitro to either alloantigens or tumor antigens.体外对同种抗原或肿瘤抗原致敏的淋巴细胞的特异性刺激和细胞毒性作用。
J Immunol. 1975 Mar;114(3):1083-8.
6
Cell-mediated cytotoxicity of adherent and non-adherent mouse lymph node cells sensitized in vitro against tumour-associated antigens of syngenetic methylcholanthrene-induced sarcomas.体外致敏的贴壁和非贴壁小鼠淋巴结细胞对同基因甲基胆蒽诱导肉瘤的肿瘤相关抗原的细胞介导细胞毒性。
Folia Biol (Praha). 1979;25(2):137-41.
7
Effect of Nocardia rubra cell wall skeleton on T-cell-mediated cytotoxicity in mice bearing syngeneic sarcoma.红色诺卡氏菌细胞壁骨架对同基因肉瘤小鼠T细胞介导的细胞毒性的影响。
Cancer Res. 1981 Feb;41(2):660-6.
8
Phenotype analyses and cellular mechanisms of the pre-effector T-lymphocyte response to a progressive syngeneic murine sarcoma.效应前体T淋巴细胞对进行性同基因小鼠肉瘤反应的表型分析及细胞机制
Cancer Res. 1990 Jul 15;50(14):4371-6.
9
Generation from tumor-bearing mice of lymphocytes with in vivo therapeutic efficacy.从荷瘤小鼠体内生成具有体内治疗效果的淋巴细胞。
J Immunol. 1987 Jul 1;139(1):295-304.
10
Methylcholanthrene-induced mouse sarcomas express individually distinct major histocompatibility complex class I-associated peptides recognized by specific CD8+ T-cell lines.甲基胆蒽诱导的小鼠肉瘤表达出各自独特的与主要组织相容性复合体I类相关的肽段,这些肽段可被特定的CD8 + T细胞系识别。
Cancer Res. 1995 Dec 1;55(23):5648-55.

引用本文的文献

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Methylcholanthrene-Induced Sarcomas Develop Independently from NOX2-Derived ROS.甲基胆蒽诱导的肉瘤独立于NOX2衍生的活性氧生成。
PLoS One. 2015 Jun 15;10(6):e0129786. doi: 10.1371/journal.pone.0129786. eCollection 2015.