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用于定量牛奥斯特他线虫病细胞免疫反应的有限稀释分析

Limiting dilution analyses for the quantification of cellular immune responses in bovine ostertagiasis.

作者信息

Gasbarre L C

出版信息

Vet Parasitol. 1986 Mar;20(1-3):133-47. doi: 10.1016/0304-4017(86)90097-x.

Abstract

A sensitive limiting dilution analysis (LDA) was used to quantitate the local and systemic cellular immune response of cattle after immunization with keyhole limpet hemocyanin (KLH) and infection with Ostertagia ostertagi. The assay measures the proliferative response of bovine T-cells after in vitro stimulation with antigen. Interleukin 2 activity was supplied by supernates from mitogen-stimulated bovine peripheral blood lymphocytes (PBL) and accessory cell function was in the form of irradiated autologous PBL. The assay measures the response of a single cell and was most easily demonstrated in the lymph nodes draining the site of antigen inoculation. Comparison of cell frequencies and maximal responses generated in conventional proliferative assays showed several differences between the two assays. First, after antigen injection, the highest cell frequencies were seen in the draining lymph nodes within 3 days, and decreased by 10 days post-immunization. In contrast, in mass cultures maximal stimulation was not seen until 7-10 days after injection, but remained high up to 4 weeks after immunization. Second, at 17 days post-infection, a time of eruption of the parasite from the gastric glands, high frequencies of inducible cells were demonstrated by LDA in all lymphoid populations tested. In contrast, low levels of proliferation were seen in mass cultures. The reasons for these differences may include different sensitivities to suppression or more stringent requirements for specificity between the two assays. Finally, it was found that immunologically naive calves have relatively high frequencies of Ostertagia-specific cells in PBL, and that after infection these frequencies decrease. These results indicate either active suppression of the potential anti-Ostertagia response or an extra-vascularization of these cells to the site of infection.

摘要

采用灵敏的有限稀释分析(LDA)来定量检测牛在用钥孔戚血蓝蛋白(KLH)免疫和感染奥斯特他线虫后局部和全身的细胞免疫反应。该检测方法可测量体外抗原刺激后牛T细胞的增殖反应。白细胞介素2活性由丝裂原刺激的牛外周血淋巴细胞(PBL)的上清液提供,辅助细胞功能则以经辐照的自体PBL的形式存在。该检测方法可测量单个细胞的反应,并且在抗原接种部位引流的淋巴结中最容易得到证实。对传统增殖检测中产生的细胞频率和最大反应进行比较,结果显示这两种检测方法存在若干差异。首先,抗原注射后,在3天内引流淋巴结中的细胞频率最高,免疫后10天细胞频率下降。相比之下,在大量培养中,直到注射后7 - 10天才出现最大刺激,但在免疫后4周内一直保持较高水平。其次,在感染后17天,即寄生虫从胃腺中逸出的时期,LDA在所有测试的淋巴样群体中均显示出高频率的可诱导细胞。相比之下,大量培养中观察到的增殖水平较低。这些差异的原因可能包括对抑制的不同敏感性或两种检测方法对特异性的更严格要求。最后,发现免疫未接触过抗原的犊牛外周血淋巴细胞中奥斯特他线虫特异性细胞的频率相对较高,感染后这些频率会降低。这些结果表明,要么是对潜在的抗奥斯特他线虫反应进行了主动抑制,要么是这些细胞向感染部位发生了血管外渗。

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