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布鲁氏菌流产抗原体外刺激牛淋巴细胞的动力学

Kinetics of in vitro bovine lymphocyte immunostimulation with a Brucella abortus antigen.

作者信息

Kaneene J M, Johnson D W, Anderson R K, Angus R D, Pietz D E, Muscoplat C C

出版信息

Am J Vet Res. 1978 Feb;39(2):235-9.

PMID:415646
Abstract

A Brucella abortus-soluble antigen was investigated, using in vitro assay of lymphocyte immunostimulation, to determine which concentration of this antigen and which period of incubation of the lymphocyte cultures would induce maximum specific lymphocyte immunostimulation as an additional method for further study of B abortus infection in cattle. Soluble antigen was prepared from autoclaved cells of B abortus strain 1119-3. Peripheral blood lymphocytes were obtained from cattle infected with B abortus and from healthy control cattle not infected with B abortus. The lymphocytes were prepared by the Ficoll-Hypaque density gradient technique, suspended in RPMI 1640 medium (1.5 X 10(6)/ml), cultured with several dilutions of soluble antigen, and incubated. Prior to termination of incubation, cultures were labeled with 1 muCi of [3H]thymidine and, after harvesting, assayed for [3H]thymidine incorporation in DNA by a liquid scintillation spectrometer. Maximum specific immunostimulation of lymphocytes from B abortus-infected cattle was induced in this assay system with 6 days' incubation and 22 microgram of protein/ml/1.5 X 10(6) lymphocytes, using protein content to express concentration of soluble antigen in this system.

摘要

研究了一种流产布鲁氏菌可溶性抗原,采用淋巴细胞免疫刺激体外试验,以确定该抗原的哪种浓度以及淋巴细胞培养的哪个孵育期会诱导最大的特异性淋巴细胞免疫刺激,作为进一步研究牛流产布鲁氏菌感染的一种额外方法。可溶性抗原由流产布鲁氏菌1119 - 3菌株的高压灭菌细胞制备。外周血淋巴细胞取自感染流产布鲁氏菌的牛和未感染流产布鲁氏菌的健康对照牛。淋巴细胞通过Ficoll - Hypaque密度梯度技术制备,悬浮于RPMI 1640培养基(1.5×10⁶/毫升)中,与几种可溶性抗原稀释液一起培养并孵育。在孵育结束前,用1微居里的[³H]胸腺嘧啶核苷标记培养物,收获后,用液体闪烁光谱仪测定DNA中[³H]胸腺嘧啶核苷的掺入量。在该试验系统中,对于感染流产布鲁氏菌的牛的淋巴细胞,孵育6天且使用22微克蛋白质/毫升/1.5×10⁶淋巴细胞时诱导出最大的特异性免疫刺激,在该系统中用蛋白质含量表示可溶性抗原的浓度。

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