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NZB小鼠中细胞毒性淋巴细胞体外发育随年龄的下降。

Age-associated decline in the in vitro development of cytotoxic lymphocytes in NZB mice.

作者信息

Hirano T, Nordin A A

出版信息

J Immunol. 1976 Oct;117(4):1093-8.

PMID:135807
Abstract

The development of cytotoxic lymphocytes (CL) in in vitro mixed lymphocyte culture (MLC) was investigated in young (14 weeks), middle (40 weeks), and aged (80 weeks) NZB mice. Cytotoxic activity against H-2B alloantigens was measured by using the 51Cr release assay. The antigen dose to elicit the optimum development of CL in vitro was the same for all ages of NZB mice, but the level of the development of CL was consistently low and could be delayed by up to 24 hr in aged mice. This decline in the frequency of autoantibody against red blood cells nor to the decrease of the frequency of omega-positive cells in aged NZB mice. Aged (83 weeks) DBA/2 mice showed a similar decline in the development of CL. This decline of T cell function in aged NZB mice might be related to a physiologic aging process rather than to autoimmune disease.

摘要

在年轻(14周龄)、中年(40周龄)和老年(80周龄)的新西兰黑鼠(NZB)中,研究了体外混合淋巴细胞培养(MLC)中细胞毒性淋巴细胞(CL)的发育情况。通过使用51Cr释放试验来测量针对H-2B同种抗原的细胞毒性活性。引发CL体外最佳发育的抗原剂量在所有年龄段的NZB小鼠中都是相同的,但CL的发育水平一直较低,并且在老年小鼠中可能会延迟长达24小时。这种情况既不是由于老年NZB小鼠中抗红细胞自身抗体频率的下降,也不是由于ω阳性细胞频率的降低。老年(83周龄)的DBA/2小鼠在CL的发育中也表现出类似的下降。老年NZB小鼠中T细胞功能的这种下降可能与生理衰老过程有关,而不是与自身免疫性疾病有关。

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