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实验性梅毒期间针对梅毒螺旋体个体可溶性抗原的细胞免疫发展

Development of cellular immunity to individual soluble antigens of Treponema pallidum during experimental syphilis.

作者信息

Baker-Zander S A, Fohn M J, Lukehart S A

机构信息

Department of Medicine, School of Medicine, University of Washington, Seattle 98195.

出版信息

J Immunol. 1988 Dec 15;141(12):4363-9.

PMID:2461990
Abstract

The contribution of individual specific molecules of Treponema pallidum subspecies pallidum to cellular immunity in experimental syphilis was evaluated by combining the techniques of Ag identification and purification with the lymphocyte proliferation assay. Proliferative responses of splenic lymphocytes from syphilitic rabbits to complex treponemal Ag and Con A were vigorous throughout the course of intratesticular infection (6, 10, 17, 30, and 210 days). Normal rabbits did not respond to any treponemal preparations and all rabbits failed to respond to normal rabbit testicular Ag (NRT). Seven defined treponemal Ag (47 kDa, 37 kDa, 35, 33-kDa, 30-kDa, 14 kDa, and 12 kDa) stimulated lymphocytes from infected rabbits. Cellular responses to the 37-kDa and 30-kDa fractions were evident by day 6 of infection and responses to the 35, 33-kDa and 14-kDa Ag were first detected on day 10; responsiveness to these Ag continued throughout the observation period. Cellular responses to the 47-kDa molecule were detectable but lower when compared with other individual Ag. Responsiveness to the 12-kDa Ag was not evident until 7 mo postinfection. Specific immunoblot reactivity of serum from rabbits used in this study generally correlated with the development of cellular reactivity to individual Ag of T. pallidum.

摘要

通过将抗原鉴定与纯化技术和淋巴细胞增殖试验相结合,评估了梅毒螺旋体苍白亚种的单个特定分子对实验性梅毒细胞免疫的贡献。在睾丸内感染过程中(第6、10、17、30和210天),梅毒兔脾淋巴细胞对复合梅毒抗原和刀豆蛋白A的增殖反应一直很强。正常兔对任何梅毒制剂均无反应,所有兔对正常兔睾丸抗原(NRT)均无反应。七种确定的梅毒抗原(47 kDa、37 kDa、3 kDa、33 kDa、30 kDa、14 kDa和12 kDa)刺激感染兔的淋巴细胞。感染第6天,对37 kDa和30 kDa组分的细胞反应明显,对35、33 kDa和14 kDa抗原的反应在第10天首次检测到;在整个观察期内对这些抗原的反应持续存在。与其他单个抗原相比,对47 kDa分子的细胞反应可检测到但较低。对12 kDa抗原的反应直到感染后7个月才明显。本研究中所用兔血清的特异性免疫印迹反应性通常与对梅毒螺旋体单个抗原的细胞反应性的发展相关。

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