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Role of TNF-alpha in CD8+ cytotoxic T lymphocyte-mediated lysis.肿瘤坏死因子-α在CD8 + 细胞毒性T淋巴细胞介导的细胞裂解中的作用。
J Immunol. 1993 May 15;150(10):4303-14.
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Mechanisms of rejection induced by tumor cell-targeted gene transfer of interleukin 2, interleukin 4, interleukin 7, tumor necrosis factor, or interferon gamma.白细胞介素2、白细胞介素4、白细胞介素7、肿瘤坏死因子或干扰素γ的肿瘤细胞靶向基因转移诱导的排斥机制。
Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2774-8. doi: 10.1073/pnas.90.7.2774.
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CD2/LFA-3 or LFA-1/ICAM-1 but not CD28/B7 interactions can augment cytotoxicity by virus-specific CD8+ cytotoxic T lymphocytes.CD2/LFA - 3或LFA - 1/ICAM - 1相互作用而非CD28/B7相互作用可增强病毒特异性CD8 + 细胞毒性T淋巴细胞的细胞毒性。
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In situ detection of activated cytotoxic cells in follicular lymphomas.滤泡性淋巴瘤中活化细胞毒性细胞的原位检测。
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Constant-infusion recombinant interleukin-2 in adoptive immunotherapy of advanced cancer.持续输注重组白细胞介素-2在晚期癌症过继性免疫治疗中的应用
N Engl J Med. 1987 Apr 9;316(15):898-905. doi: 10.1056/NEJM198704093161502.
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A progress report on the treatment of 157 patients with advanced cancer using lymphokine-activated killer cells and interleukin-2 or high-dose interleukin-2 alone.关于使用淋巴因子激活的杀伤细胞和白细胞介素-2或单独使用高剂量白细胞介素-2治疗157例晚期癌症患者的进展报告。
N Engl J Med. 1987 Apr 9;316(15):889-97. doi: 10.1056/NEJM198704093161501.
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A novel form of TNF/cachectin is a cell surface cytotoxic transmembrane protein: ramifications for the complex physiology of TNF.一种新型的肿瘤坏死因子/恶病质素是一种细胞表面细胞毒性跨膜蛋白:对肿瘤坏死因子复杂生理学的影响。
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The importance of tamoxifen to a cisplatin-containing regimen in the treatment of metastatic melanoma.
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IL-2 induces expression of serine protease enzymes and genes in natural killer and nonspecific T killer cells.白细胞介素-2可诱导自然杀伤细胞和非特异性T杀伤细胞中丝氨酸蛋白酶及相关基因的表达。
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10
Perforin and serine esterase gene expression in stimulated human T cells. Kinetics, mitogen requirements, and effects of cyclosporin A.活化的人T细胞中穿孔素和丝氨酸酯酶基因的表达。动力学、丝裂原需求及环孢素A的影响。
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重组白细胞介素-2治疗的转移性黑色素瘤患者中穿孔素和颗粒酶B基因表达增加。

Increased expression of perforin and granzyme B genes in patients with metastatic melanoma treated with recombinant interleukin-2.

作者信息

Leger-Ravet M B, Mathiot C, Portier A, Brandely M, Galanaud P, Fridman W H, Emilie D

机构信息

INSERM U131, Clamart, France.

出版信息

Cancer Immunol Immunother. 1994 Jul;39(1):53-8. doi: 10.1007/BF01517181.

DOI:10.1007/BF01517181
PMID:8044827
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11038965/
Abstract

The frequency of peripheral blood cells expressing the perforin gene or the granzyme B gene was evaluated by in situ hybridization in nine patients suffering from metastatic melanoma and treated with recombinant interleukin-2 (rIL-2). A spontaneous expression of both genes was detected in five to seven patients. rIL-2 administration increased the frequency of positive cells in all patients (P < 0.03 for each gene), the highest frequency being reached in the patients who already expressed these genes prior to rIL-2 treatment (P < 0.02). Expressions of the granzyme B gene and of the perforin gene were strongly correlated before IL-2 treatment and they were similarly affected by rIL-2 administration. In contrast, their modification under treatment did not correlate with that of CD56+ cell counts, of natural killer activity and of sCD8 release. This indicates that perforin and granzyme B gene expressions are markers of cytotoxic cell activation independent of those previously described, and that they should be further evaluated in patients with malignancies to delineate their potential value in predicting clinical outcome.

摘要

采用原位杂交技术,对9例转移性黑色素瘤患者进行重组白细胞介素-2(rIL-2)治疗后,评估外周血中表达穿孔素基因或颗粒酶B基因的细胞频率。在5至7例患者中检测到这两种基因的自发表达。给予rIL-2后,所有患者的阳性细胞频率均增加(每个基因P<0.03),在rIL-2治疗前已表达这些基因的患者中达到最高频率(P<0.02)。颗粒酶B基因和穿孔素基因的表达在IL-2治疗前密切相关,且它们受rIL-2给药的影响相似。相比之下,治疗过程中它们的变化与CD56+细胞计数、自然杀伤活性和可溶性CD8释放的变化无关。这表明穿孔素和颗粒酶B基因表达是细胞毒性细胞激活的标志物,独立于先前描述的标志物,并且在恶性肿瘤患者中应进一步评估它们在预测临床结果中的潜在价值。