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小鼠淋巴因子激活的杀伤细胞、自然杀伤细胞和细胞毒性T淋巴细胞的比较。

Comparison of murine lymphokine-activated killer cells, natural killer cells, and cytotoxic T lymphocytes.

作者信息

Merluzzi V J

出版信息

Cell Immunol. 1985 Oct 1;95(1):95-104. doi: 10.1016/0008-8749(85)90298-9.

DOI:10.1016/0008-8749(85)90298-9
PMID:3875426
Abstract

Precursors and effectors of murine lymphokine-activated killer cells, natural killer cells, and cytotoxic T lymphocytes are compared. Natural killer cells are resistant to gamma-irradiation (1000 R) whereas precursors of lymphokine-activated killer cells and cytotoxic T lymphocytes are sensitive. Lower doses of gamma-irradiation (500 R) remove precursors for cytotoxic T lymphocytes but not lymphokine-activated killer cells. In addition, lymphokine-activated killer cells are regenerated before classical CTL after sublethal doses of gamma-irradiation. Natural killer cells are resistant to anti-Thy 1 and C' and anti-thymocyte serum, but sensitive to anti-asialo GM1 and complement. Precursors of cytotoxic T lymphocytes are sensitive to anti-Thy 1 and complement and anti-thymocyte serum, but are resistant to anti-asialo GM1 and complement. Precursors of lymphokine-activated killer cells are partially sensitive to anti-Thy 1 and complement and anti-thymocyte serum, but are resistant to anti-asialo GM1 and complement. Effector cells of cytotoxic T lymphocytes are sensitive to anti-Thy 1 and complement and resistant to anti-asialo GM1 and complement. Lymphokine-activated killer cell effectors are sensitive to anti-asialo GM1 and complement at 24 hr after activation. These effectors are more closely aligned with classical natural killer effectors. Lymphokine-activated killer effectors, 7 days after activation, are resistant to anti-asialo GM1 and complement and sensitive to anti-Thy 1 and complement. Relationships and differences among these cytotoxic subsets are discussed.

摘要

对小鼠淋巴因子激活的杀伤细胞、自然杀伤细胞和细胞毒性T淋巴细胞的前体细胞和效应细胞进行了比较。自然杀伤细胞对γ射线照射(1000拉德)具有抗性,而淋巴因子激活的杀伤细胞和细胞毒性T淋巴细胞的前体细胞则敏感。较低剂量的γ射线照射(500拉德)可去除细胞毒性T淋巴细胞的前体细胞,但不会去除淋巴因子激活的杀伤细胞的前体细胞。此外,在亚致死剂量的γ射线照射后,淋巴因子激活的杀伤细胞比经典的细胞毒性T淋巴细胞更早再生。自然杀伤细胞对抗Thy 1和补体以及抗胸腺细胞血清具有抗性,但对抗唾液酸GM1和补体敏感。细胞毒性T淋巴细胞的前体细胞对抗Thy 1和补体以及抗胸腺细胞血清敏感,但对抗唾液酸GM1和补体具有抗性。淋巴因子激活的杀伤细胞的前体细胞对抗Thy 1和补体以及抗胸腺细胞血清部分敏感,但对抗唾液酸GM1和补体具有抗性。细胞毒性T淋巴细胞的效应细胞对抗Thy 1和补体敏感,对抗唾液酸GM1和补体具有抗性。淋巴因子激活的杀伤细胞效应细胞在激活后24小时对抗唾液酸GM1和补体敏感。这些效应细胞与经典的自然杀伤效应细胞更为相似。激活7天后的淋巴因子激活的杀伤细胞效应细胞对抗唾液酸GM1和补体具有抗性,对抗Thy 1和补体敏感。讨论了这些细胞毒性亚群之间的关系和差异。

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Comparison of murine lymphokine-activated killer cells, natural killer cells, and cytotoxic T lymphocytes.小鼠淋巴因子激活的杀伤细胞、自然杀伤细胞和细胞毒性T淋巴细胞的比较。
Cell Immunol. 1985 Oct 1;95(1):95-104. doi: 10.1016/0008-8749(85)90298-9.
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Lymphokine-activated killer (LAK) cells. II. Delineation of distinct murine LAK-precursor subpopulations.淋巴因子激活的杀伤细胞(LAK细胞)。II. 不同小鼠LAK前体细胞亚群的描绘。
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Murine lymphokine-activated killer (LAK) cells: phenotypic characterization of the precursor and effector cells.小鼠淋巴因子激活的杀伤(LAK)细胞:前体细胞和效应细胞的表型特征
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A subpopulation of allospecific cytotoxic T-cell precursors with phenotypic characteristics of natural killer cells.具有自然杀伤细胞表型特征的同种特异性细胞毒性T细胞前体亚群。
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Effect of rabbit anti-asialo GM1 treatment in vivo or with anti-asialo GM1 plus complement in vitro on cytotoxic T cell activities.兔抗去唾液酸GM1体内治疗或抗去唾液酸GM1加补体体外治疗对细胞毒性T细胞活性的影响。
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Flow cytometric analysis reveals the presence of asialo GM1 on the surface membrane of alloimmune cytotoxic T lymphocytes.流式细胞术分析显示同种免疫细胞毒性T淋巴细胞表面膜上存在脱唾液酸GM1。
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Differential expression of asialo GM1 on alloreactive cytotoxic T lymphocytes and lymphokine-activated killer cells.去唾液酸GM1在同种异体反应性细胞毒性T淋巴细胞和淋巴因子激活的杀伤细胞上的差异表达。
Cell Immunol. 1987 Jan;104(1):115-25. doi: 10.1016/0008-8749(87)90012-8.

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