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1
Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. II. T lymphocyte-mediated cytolysis.通过对小鼠肥大细胞瘤P815进行诱变获得的免疫原性变体。II. T淋巴细胞介导的细胞溶解作用。
J Exp Med. 1980 Nov 1;152(5):1184-93. doi: 10.1084/jem.152.5.1184.
2
Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. I. Rejection by syngeneic mice.通过对小鼠肥大细胞瘤P815进行诱变获得的免疫原性变体。I. 同基因小鼠的排斥反应。
J Exp Med. 1980 Nov 1;152(5):1175-83. doi: 10.1084/jem.152.5.1175.
3
Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. VI. Occasional escape from host rejection due to antigen-loss secondary variants.通过对小鼠肥大细胞瘤P815进行诱变获得的免疫原性变体。VI. 由于抗原缺失继发变体导致偶尔逃避宿主排斥反应。
Int J Cancer. 1983 Jan 15;31(1):119-23. doi: 10.1002/ijc.2910310119.
4
Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. VII. Dominant expression of variant antigens in somatic cell hybrids.通过对小鼠肥大细胞瘤P815进行诱变获得的免疫原性变体。VII. 变体抗原在体细胞杂种中的显性表达。
Somatic Cell Genet. 1983 May;9(3):345-57. doi: 10.1007/BF01539143.
5
Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. IV. Analysis of variant-specific antigens by selection of antigen-loss variants with cytolytic T cell clones.通过对小鼠肥大细胞瘤P815进行诱变获得的免疫原性变体。IV. 用细胞溶解T细胞克隆选择抗原缺失变体分析变体特异性抗原。
Eur J Immunol. 1982 May;12(5):406-12. doi: 10.1002/eji.1830120509.
6
Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. III. Clonal analysis of the syngeneic cytolytic T lymphocyte response.通过对小鼠肥大细胞瘤P815进行诱变获得的免疫原性变体。III. 同基因细胞溶解型T淋巴细胞反应的克隆分析。
Eur J Immunol. 1982 May;12(5):401-6. doi: 10.1002/eji.1830120508.
7
Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. V. H-2 associativity of variant-specific antigens.通过对小鼠肥大细胞瘤P815进行诱变获得的免疫原性变体。V. 变体特异性抗原的H-2关联性
Eur J Immunol. 1982 Nov;12(11):905-8. doi: 10.1002/eji.1830121102.
8
Immunogenic (tum-) variants obtained by mutagenesis of mouse mastocytoma P815. VIII. Detection of stable transfectants expressing a tum- antigen with a cytolytic T cell stimulation assay.通过对小鼠肥大细胞瘤P815进行诱变获得的免疫原性(肿瘤 - )变体。VIII. 用细胞溶解T细胞刺激试验检测表达肿瘤抗原的稳定转染子。
Immunogenetics. 1987;26(3):178-87. doi: 10.1007/BF00365909.
9
Tumour cell variants with increased immunogenicity obtained by mutagen treatment.通过诱变处理获得的具有增强免疫原性的肿瘤细胞变体。
Cancer Surv. 1985;4(1):135-48.
10
Increased frequency of immunogenic variants obtained by repeated mutagen treatment of mouse mastocytoma P815.通过对小鼠肥大细胞瘤P815进行反复诱变处理获得的免疫原性变体频率增加。
Eur J Cancer Clin Oncol. 1983 Nov;19(11):1529-37. doi: 10.1016/0277-5379(83)90082-2.

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1
Multiplex bead-based measurement of humoral immune responses against tumor-associated antigens in stage II melanoma patients of the EORTC18961 trial.在EORTC18961试验的II期黑色素瘤患者中,基于多重微珠的针对肿瘤相关抗原的体液免疫反应测量。
Oncoimmunology. 2018 Feb 12;7(6):e1428157. doi: 10.1080/2162402X.2018.1428157. eCollection 2018.
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Tumour antigens recognized by T lymphocytes: at the core of cancer immunotherapy.T 淋巴细胞识别的肿瘤抗原:癌症免疫治疗的核心。
Nat Rev Cancer. 2014 Feb;14(2):135-46. doi: 10.1038/nrc3670.
3
Targets for active immunotherapy against pediatric solid tumors.针对儿童实体瘤的主动免疫疗法靶点。
Cancer Immunol Immunother. 2009 Jun;58(6):831-41. doi: 10.1007/s00262-008-0619-x. Epub 2008 Nov 14.
4
Molecular cancer vaccines: Tumor therapy using antigen-specific immunizations.分子癌症疫苗:利用抗原特异性免疫的肿瘤治疗。
Pathol Oncol Res. 1997 Sep;3(3):164-76. doi: 10.1007/BF02899917.
5
A new tumor-specific antigen encoded by MAGE-C2 and presented to cytolytic T lymphocytes by HLA-B44.一种由MAGE-C2编码并由HLA-B44呈递给细胞毒性T淋巴细胞的新型肿瘤特异性抗原。
Cancer Immunol Immunother. 2007 Jun;56(6):753-9. doi: 10.1007/s00262-006-0244-5. Epub 2006 Nov 10.
6
Identification of a new HLA-A*0201-restricted cytotoxic T lymphocyte epitope from CML28.从CML28中鉴定出一种新的HLA-A*0201限制性细胞毒性T淋巴细胞表位。
Cancer Immunol Immunother. 2006 Dec;55(12):1575-83. doi: 10.1007/s00262-006-0152-8. Epub 2006 Mar 14.
7
A CASP-8 mutation recognized by cytolytic T lymphocytes on a human head and neck carcinoma.一种在人类头颈癌上被细胞毒性T淋巴细胞识别的半胱天冬酶8(CASP-8)突变。
J Exp Med. 1997 Aug 29;186(5):785-93. doi: 10.1084/jem.186.5.785.
8
A new gene coding for an antigen recognized by autologous cytolytic T lymphocytes on a human renal carcinoma.一种编码人类肾癌上被自体细胞溶解性T淋巴细胞识别的抗原的新基因。
Immunogenetics. 1996;44(5):323-30. doi: 10.1007/BF02602776.
9
Regulatory mechanisms of antitumor T cell responses in the tumor-bearing state.荷瘤状态下抗肿瘤T细胞反应的调节机制。
Immunol Res. 1995;14(4):271-91. doi: 10.1007/BF02935625.
10
A mutated HLA-A2 molecule recognized by autologous cytotoxic T lymphocytes on a human renal cell carcinoma.一种在人肾细胞癌上被自体细胞毒性T淋巴细胞识别的突变HLA - A2分子。
J Exp Med. 1996 Jun 1;183(6):2501-8. doi: 10.1084/jem.183.6.2501.

本文引用的文献

1
Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. I. Rejection by syngeneic mice.通过对小鼠肥大细胞瘤P815进行诱变获得的免疫原性变体。I. 同基因小鼠的排斥反应。
J Exp Med. 1980 Nov 1;152(5):1175-83. doi: 10.1084/jem.152.5.1175.
2
Cooperation of immune lymphoid cells with macrophages in tumour immunity.免疫淋巴细胞与巨噬细胞在肿瘤免疫中的协同作用。
Nature. 1970 Nov 14;228(5272):620-2. doi: 10.1038/228620a0.
3
Role of macrophages in tumour immunity. I. Co-operation between macrophages and lymphoid cells in syngeneic tumour immunity.巨噬细胞在肿瘤免疫中的作用。I. 巨噬细胞与淋巴细胞在同基因肿瘤免疫中的协作。
Immunology. 1972 Oct;23(4):615-26.
4
The lymphocyte response to primary Moloney sarcoma virus tumors in BALB-c mice. Definition of the active subpopulations at different times after infection.BALB-c小鼠对原发性莫洛尼肉瘤病毒肿瘤的淋巴细胞反应。感染后不同时间活性亚群的定义。
J Exp Med. 1973 Jun 1;137(6):1472-93. doi: 10.1084/jem.137.6.1472.
5
A rapid method for the isolation of functional thymus-derived murine lymphocytes.一种分离功能性胸腺来源的小鼠淋巴细胞的快速方法。
Eur J Immunol. 1973 Oct;3(10):645-9. doi: 10.1002/eji.1830031011.
6
Cell-mediated immune reaction against tumors induced by oncornaviruses. II. Nature of the effector cells in tumor-cell cytolysis.针对肿瘤病毒诱导的肿瘤的细胞介导免疫反应。II. 肿瘤细胞溶解中效应细胞的性质。
Int J Cancer. 1973 Mar 15;11(2):426-32. doi: 10.1002/ijc.2910110220.
7
Generation of cytotoxic T lymphocytes in vitro. I. Response of normal and immune mouse spleen cells in mixed leukocyte cultures.体外细胞毒性T淋巴细胞的产生。I. 混合白细胞培养中正常和免疫小鼠脾细胞的反应。
J Exp Med. 1974 Sep 1;140(3):703-17. doi: 10.1084/jem.140.3.703.
8
"Natural" killer cells in the mouse. I. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Specificity and distribution according to genotype.小鼠中的“天然”杀伤细胞。I. 对小鼠莫洛尼白血病细胞具有特异性的细胞毒性细胞。根据基因型的特异性和分布。
Eur J Immunol. 1975 Feb;5(2):112-7. doi: 10.1002/eji.1830050208.
9
In vitro induction of cytotoxicity against syngeneic mastocytoma and its suppression by spleen and thymus cells from tumor-bearing mice.体外诱导对同基因肥大细胞瘤的细胞毒性及其被荷瘤小鼠的脾细胞和胸腺细胞抑制的情况。
J Immunol. 1976 Feb;116(2):288-93.
10
Cytotoxic T-cell responses to H-Y: correlation with the rejection of syngeneic male skin grafts.细胞毒性T细胞对H-Y的反应:与同基因雄性皮肤移植排斥反应的相关性。
J Exp Med. 1978 Mar 1;147(3):768-75. doi: 10.1084/jem.147.3.768.

通过对小鼠肥大细胞瘤P815进行诱变获得的免疫原性变体。II. T淋巴细胞介导的细胞溶解作用。

Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815. II. T lymphocyte-mediated cytolysis.

作者信息

Boon T, Van Snick J, Van Pel A, Uyttenhove C, Marchand M

出版信息

J Exp Med. 1980 Nov 1;152(5):1184-93. doi: 10.1084/jem.152.5.1184.

DOI:10.1084/jem.152.5.1184
PMID:6776227
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2186002/
Abstract

Tumor cell variants that were rejected by syngeneic mice (tum-) were obtained from mastocytoma P815 by mutagenesis (as described in the accompanying report (13). A considerable T lymphocyte-mediated lysis was observed upon incubation of these tum- variants with peritoneal exudate cells collected a few days after an intraperitoneal challenge of immune animals. Spleen cells from these animals were cytolytic after stimulation in vitro with the immunizing variant. New antigens, absent from the original P815 tum+ cells, were detected on 15 of the 21 tum- variants that were tested. All these antigens appeared to be different. No new antigen was detected on any of 10 mutagenized P815 clones that had retained their ability to form tumors. We compared the evidence obtained in vivo and in vitro for the presence of specific antigens on five tum- variants. Three variants were shown both in vivo and in vitro to carry an individual antigen. One showed no specificity either in vivo or in vitro. However, for one variant, no specificity was observed in vivo, although cytolysis tests demonstrated the existence of a singular antigenic specificity.

摘要

通过诱变从肥大细胞瘤P815获得被同基因小鼠排斥的肿瘤细胞变体(tum-)(如随附报告(13)中所述)。将这些tum-变体与免疫动物腹腔内攻击后几天收集的腹腔渗出细胞一起孵育时,观察到相当程度的T淋巴细胞介导的裂解。这些动物的脾细胞在体外用免疫变体刺激后具有细胞溶解性。在测试的21个tum-变体中的15个上检测到原始P815 tum+细胞中不存在的新抗原。所有这些抗原似乎都不同。在10个保留形成肿瘤能力的诱变P815克隆中,没有一个检测到新抗原。我们比较了在体内和体外获得的关于五个tum-变体上存在特异性抗原的证据。三个变体在体内和体外均显示携带单个抗原。一个在体内和体外均未显示出特异性。然而,对于一个变体,尽管细胞溶解试验证明存在单一抗原特异性,但在体内未观察到特异性。