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甲状腺过氧化物酶与自身免疫性甲状腺疾病的诱导

Thyroid peroxidase and the induction of autoimmune thyroid disease.

作者信息

McLachlan S M, Atherton M C, Nakajima Y, Napier J, Jordan R K, Clark F, Rees Smith B

机构信息

Department of Medicine, University of Wales College of Medicine, Cardiff.

出版信息

Clin Exp Immunol. 1990 Feb;79(2):182-8. doi: 10.1111/j.1365-2249.1990.tb05176.x.

Abstract

Animal models of autoimmune thyroid disease are associated with thyroglobulin (Tg) as autoantigen whereas in man the autoimmune response to microsomal antigen/thyroid peroxidase (TPO) appears to play a major role in thyroiditis. Consequently, we have compared the ability of TPO and Tg to induce thyroid autoantibodies and thyroid damage in mice known to be susceptible (CBA/J) or resistant (BALB/c) to thyroiditis induced using murine Tg. Groups of three to five mice were immunized twice using Freund's complete adjuvant with 80-100 micrograms highly purified porcine (p) TPO, pTg, rat (r) Tg, human Tg, bovine serum albumin (BSA) or BSA + 0.2 micrograms pTg (the level of Tg contamination of TPO). Four weeks after immunization with TPO, plasma from CBA/J (but not BALB/c) mice contained IgG class antibodies which bound to TPO-coated tubes in the presence or absence of excess Tg (and could therefore be clearly distinguished from Tg antibodies) but there was no evidence of thyroiditis in either strain of mice. In contrast, in CBA/J mice immunized with rTg and, to a lesser extent in mice that had received pTg, thyroid tissue was infiltrated with lymphoid cells and/or neutrophils and antibodies to pTg (but not pTPO) were present. Our observations demonstrate that induction of TPO antibody alone is insufficient to lead to thyroiditis in CBA/J mice. Further, these studies emphasize the complex interactions between MHC and different thyroid antigens in the processes leading to thyroid destruction.

摘要

自身免疫性甲状腺疾病的动物模型与作为自身抗原的甲状腺球蛋白(Tg)相关,而在人类中,针对微粒体抗原/甲状腺过氧化物酶(TPO)的自身免疫反应似乎在甲状腺炎中起主要作用。因此,我们比较了TPO和Tg在已知对使用鼠Tg诱导的甲状腺炎敏感(CBA/J)或抗性(BALB/c)的小鼠中诱导甲状腺自身抗体和甲状腺损伤的能力。将三到五只小鼠分为一组,用弗氏完全佐剂免疫两次,分别注射80-100微克高度纯化的猪(p)TPO、pTg、大鼠(r)Tg、人Tg、牛血清白蛋白(BSA)或BSA + 0.2微克pTg(TPO中Tg的污染水平)。用TPO免疫四周后,CBA/J(但不是BALB/c)小鼠的血浆中含有IgG类抗体,该抗体在存在或不存在过量Tg的情况下均与包被TPO的试管结合(因此可以与Tg抗体清楚区分),但两种品系的小鼠均无甲状腺炎的证据。相比之下,在用rTg免疫的CBA/J小鼠中,以及在较小程度上在接受pTg的小鼠中,甲状腺组织被淋巴细胞和/或中性粒细胞浸润,并且存在针对pTg(而非pTPO)的抗体。我们的观察结果表明,单独诱导TPO抗体不足以导致CBA/J小鼠发生甲状腺炎。此外,这些研究强调了MHC与不同甲状腺抗原在导致甲状腺破坏的过程中的复杂相互作用。

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