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1
Proliferative and cytotoxic immune functions in ageing mice. I. Sequence of decline of reactivities measured under optimal and suboptimal sensitization conditions.衰老小鼠的增殖和细胞毒性免疫功能。I. 在最佳和次优致敏条件下所测反应性的衰退顺序。
Immunology. 1981 Nov;44(3):607-16.
2
Proliferative and cytotoxic immune functions in aging mice. II. Decreased generation of specific suppressor cells in alloreactive cultures.衰老小鼠的增殖性和细胞毒性免疫功能。II. 同种异体反应性培养物中特异性抑制细胞生成减少。
J Immunol. 1984 Oct;133(4):1782-7.
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Age-associated decline in the in vitro development of cytotoxic lymphocytes in NZB mice.NZB小鼠中细胞毒性淋巴细胞体外发育随年龄的下降。
J Immunol. 1976 Oct;117(4):1093-8.
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H-2K/H-2D and Mls and I region-associated antigens stimulate helper factor(s) involved in the generation of cytotoxic T lymphocytes.H-2K/H-2D以及Mls和I区相关抗原刺激参与细胞毒性T淋巴细胞生成的辅助因子。
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6
Generation of cytotoxic T lymphocytes in vitro. VII. Suppressive effect of irradiated MLC cells on CTL response.体外细胞毒性T淋巴细胞的产生。VII. 经辐照的混合淋巴细胞培养细胞对细胞毒性T淋巴细胞反应的抑制作用。
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Proliferative and cytotoxic immune functions in aging mice. IV. Effects of suppressor cell populations from aged and young mice.衰老小鼠的增殖性和细胞毒性免疫功能。IV. 来自老年和年轻小鼠的抑制细胞群体的作用。
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FCS-activated blast T cells inhibit the in vitro response of memory CTL precursors to alloantigens by removal of factor(s) from MLC supernatant.FCS激活的母细胞化T细胞通过去除混合淋巴细胞培养上清液中的因子来抑制记忆性CTL前体细胞对同种抗原的体外反应。
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本文引用的文献

1
Alloreactive cytotoxic T lymphocytes from aged mice express increased lysis of autologous and third-party target cells.老年小鼠的同种反应性细胞毒性T淋巴细胞对自体和第三方靶细胞的裂解作用增强。
J Immunol. 1980 Aug;125(2):858-64.
2
Immunologic deficiencies in senescence. I. Characterization of intrinsic deficiencies.衰老过程中的免疫缺陷。I. 内在缺陷的特征描述。
J Immunol. 1972 Feb;108(2):403-12.
3
Quantitative assay of the lytic action of immune lymphoid cells on 51-Cr-labelled allogeneic target cells in vitro; inhibition by isoantibody and by drugs.体外定量测定免疫淋巴细胞对51-铬标记的同种异体靶细胞的溶解作用;同种抗体和药物的抑制作用。
Immunology. 1968 Feb;14(2):181-96.
4
Decline in mixed lymphocyte reactivity of spleen cells from aged mice of a long-lived strain.长寿品系老年小鼠脾细胞混合淋巴细胞反应性下降。
J Immunol. 1973 May;110(5):1216-21.
5
Comparison of irradiated and mitomycin-treated mouse spleen cells as stimulating cells in mixed lymphocyte cultures and in vitro sensitization.经辐照和丝裂霉素处理的小鼠脾细胞作为混合淋巴细胞培养和体外致敏中的刺激细胞的比较。
J Immunol. 1974 Jul;113(1):39-44.
6
A miniaturized mouse mixed leukocyte culture in serum-free and mouse serum supplemented media.一种在无血清和添加小鼠血清的培养基中的小型化小鼠混合白细胞培养。
J Immunol Methods. 1973 Oct;3(2):147-63. doi: 10.1016/0022-1759(73)90030-6.
7
The decline of cell-mediated immunity in aging mice.衰老小鼠中细胞介导免疫的衰退。
J Gerontol. 1974 Sep;29(5):499-505. doi: 10.1093/geronj/29.5.499.
8
Immune function and survival in a long-lived mouse strain subjected to undernutrition.长期营养不良的长寿小鼠品系的免疫功能与生存情况
Gerontologia. 1975;21(4):184-202. doi: 10.1159/000212044.
9
Effect of age on cell-mediated immunity in long-lived mice.年龄对长寿小鼠细胞介导免疫的影响。
Clin Exp Immunol. 1975 Mar;19(3):533-42.
10
Change of cell-mediated cytotoxicity with aging.细胞介导的细胞毒性随衰老的变化。
J Immunol. 1975 Jul;115(1):307-9.

衰老小鼠的增殖和细胞毒性免疫功能。I. 在最佳和次优致敏条件下所测反应性的衰退顺序。

Proliferative and cytotoxic immune functions in ageing mice. I. Sequence of decline of reactivities measured under optimal and suboptimal sensitization conditions.

作者信息

Gottesman S R, Kristie J A, Walford R L

出版信息

Immunology. 1981 Nov;44(3):607-16.

PMID:6459290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1554957/
Abstract

Individual young adult, middle-aged, and old C57BL/6J male mice were tested for in vitro generated proliferative and cytotoxic responses to H-2 alloantigens under a variety of sensitization conditions. Proliferation in mixed lymphocyte culture (MLC) had decreased by 14 months of age (middle-aged), whether measured by directly assaying cultures in microtitre plates (micro MLC) or by labelling aliquots taken from large culture tubes (macro MLC). Cytotoxicity did not decline until a later age if sensitization was done in large tubes (macro cell-mediated lympholysis, CML). When cytotoxic activity was assayed by measuring lysis after addition of chromated cells to MLCs in microtitre plates (micro CML), differences were revealed between young and middle-aged animals. However, these conditions were suboptimal for generation of cytotoxicity even in young controls and showed even lower responses in the middle-aged group. It was concluded that proliferation showed an earlier, more severe decline than cytotoxicity with age as the proliferative response had declined by middle-age under all sensitization conditions used. With optimal sensitization conditions, senescent mice (26--30 months) showed a four- to ten-fold decrease in cytotoxicity compared with young adult mice.

摘要

对不同年龄段的C57BL/6J雄性小鼠(包括年轻成年小鼠、中年小鼠和老年小鼠)在多种致敏条件下,测试其对H-2同种异体抗原的体外增殖反应和细胞毒性反应。无论通过微量滴定板直接检测培养物(微量混合淋巴细胞培养,micro MLC)还是标记从大培养管中取出的等分试样(宏观混合淋巴细胞培养,macro MLC)来测量,混合淋巴细胞培养(MLC)中的增殖在14月龄(中年)时就已下降。如果在大培养管中进行致敏(宏观细胞介导的淋巴细胞溶解,CML),细胞毒性直到更晚的年龄才下降。当通过在微量滴定板中将铬化细胞加入MLC后测量裂解来检测细胞毒性活性(微量细胞介导的淋巴细胞溶解,micro CML)时,年轻和中年动物之间出现了差异。然而,即使在年轻对照组中,这些条件对于细胞毒性的产生也是次优的,并且在中年组中反应更低。得出的结论是,随着年龄增长,增殖比细胞毒性更早、更严重地下降,因为在所有使用的致敏条件下,中年时增殖反应就已下降。在最佳致敏条件下,衰老小鼠(26 - 30个月)与年轻成年小鼠相比,细胞毒性降低了4至10倍。