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在用胎肝细胞重建的SCID小鼠免疫发育过程中,睾丸抗原的存在与否对实验性自身免疫性睾丸炎的调节作用。

Regulation of experimental autoimmune orchitis by the presence or absence of testicular antigens during immunological development in SCID mice reconstituted with fetal liver cells.

作者信息

Wakabayashi A, Eishi Y, Nakamura K

机构信息

Department of Pathology, Tokyo Medical and Dental University, Japan.

出版信息

Immunology. 1997 Sep;92(1):84-90. doi: 10.1046/j.1365-2567.1997.00316.x.

Abstract

Severe combined immunodeficient (SCID) mice were immunologically reconstituted by the transfer of fetal liver cells (FLC) of BALB/c mice (SCID-FLC mice). In peripheral blood (PB) of SCID-FLC mice, B and T cells started to appear 2 and 5 weeks, respectively, after the transfer of FLC, and had attained normal levels by 7 weeks. Orchidectomy and transplantation of testis under the kidney capsule were conducted at various stages of immunological maturation, and the induction of experimental autoimmune orchitis (EAO) was performed after immunological maturation in SCID-FLC mice. The experimental system was used to establish that the presence of testicular antigens in the early stage of immunological development influences the induction of EAO; grade of EAO was reduced in the presence of the antigens, and enhanced in their absence. In other words, the existence of self tissue antigens in the early stage of immunological development was essential for proper establishment of tolerance to the self tissue. These findings suggested that the SCID-FLC mouse is a suitable model with which to analyse the interaction between self antigens and cells of the developing immune system, which is otherwise observed only in the fetal or perinatal stage in experimental animals.

摘要

通过移植BALB/c小鼠的胎肝细胞(FLC)对重症联合免疫缺陷(SCID)小鼠进行免疫重建(SCID-FLC小鼠)。在SCID-FLC小鼠的外周血(PB)中,B细胞和T细胞分别在FLC移植后2周和5周开始出现,并在7周时达到正常水平。在免疫成熟的各个阶段进行睾丸切除并将睾丸移植到肾包膜下,然后在SCID-FLC小鼠免疫成熟后诱导实验性自身免疫性睾丸炎(EAO)。该实验系统用于证实免疫发育早期睾丸抗原的存在会影响EAO的诱导;抗原存在时EAO的等级降低,而抗原不存在时则增强。换句话说,免疫发育早期自身组织抗原的存在对于正确建立对自身组织的耐受性至关重要。这些发现表明,SCID-FLC小鼠是一种合适的模型,可用于分析自身抗原与发育中的免疫系统细胞之间的相互作用,而这种相互作用在实验动物中通常仅在胎儿期或围生期才能观察到。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c913/1363985/8b952604174a/immunology00049-0093-a.jpg

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