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软骨蛋白聚糖免疫在佐剂性关节炎中的作用。静脉注射牛蛋白聚糖可增强佐剂性关节炎。

The role of immunity to cartilage proteoglycan in adjuvant arthritis. Intravenous injection of bovine proteoglycan enhances adjuvant arthritis.

作者信息

Van Vollenhoven R F, Soriano A, McCarthy P E, Schwartz R L, Garbrecht F C, Thorbecke G J, Siskind G W

机构信息

Department of Medicine, Cornell University Medical College, New York 10021.

出版信息

J Immunol. 1988 Aug 15;141(4):1168-73.

PMID:3260920
Abstract

It has been suggested that autoimmunity to the proteoglycan (PG) component of cartilage plays a major role in the etiology of adjuvant arthritis (AA), which occurs in rats, but not in mice, after injection of CFA. In order to more directly investigate this role, bovine and human cartilage PG were used to modulate AA, and immunity to PG was assessed. Immunization of rats or mice with PG by itself does not induce arthritis. However, in rats, a single i.v. injection of soluble PG, given 1 wk before injection of CFA, results in a significant increase in incidence and severity of the arthritis induced. Rats injected with CFA have both antibody and delayed type hypersensitivity (DTH) to PG. Upon pretreatment of rats with PG i.v., both DTH and antibody titers to PG are increased. Rats immunized with PG in IFA have high titers of anti-PG and strong DTH to PG, which are also enhanced by pretreatment with PG i.v., although none of these animals develops arthritis. In contrast to these findings in rats, when mice are pretreated with PG i.v., DTH to PG induced by injection of CFA is lower, whereas anti-PG titers are higher than in unpretreated controls. The results presented here show that, in rats, i.v. injection of PG synergizes with CFA in the induction of AA, and enhances both humoral and cellular immunity to PG. The findings support the hypothesis that immunity to PG is of importance in AA, although under the conditions of these experiments immunity induced by PG alone is clearly not sufficient for the induction of arthritis.

摘要

有人提出,对软骨蛋白聚糖(PG)成分的自身免疫在佐剂性关节炎(AA)的病因中起主要作用,AA发生在大鼠注射完全弗氏佐剂(CFA)后,但小鼠不会发生。为了更直接地研究这一作用,使用牛和人软骨PG来调节AA,并评估对PG的免疫反应。单独用PG免疫大鼠或小鼠不会诱发关节炎。然而,在大鼠中,在注射CFA前1周静脉内单次注射可溶性PG,会导致所诱发关节炎的发病率和严重程度显著增加。注射CFA的大鼠对PG既有抗体又有迟发型超敏反应(DTH)。用PG静脉内预处理大鼠后,对PG的DTH和抗体滴度均升高。用PG在不完全弗氏佐剂(IFA)中免疫的大鼠具有高滴度的抗PG抗体和对PG的强烈DTH,静脉内用PG预处理也会增强这些反应,尽管这些动物都没有发生关节炎。与大鼠的这些发现相反,当用PG静脉内预处理小鼠时,注射CFA诱导的对PG的DTH较低,而抗PG滴度高于未预处理的对照组。此处给出的结果表明,在大鼠中,静脉内注射PG与CFA协同诱导AA,并增强对PG的体液免疫和细胞免疫。这些发现支持了对PG的免疫在AA中很重要这一假说,尽管在这些实验条件下,单独由PG诱导的免疫显然不足以诱发关节炎。

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