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暴露于伯氏疏螺旋体的巨噬细胞会在仓鼠身上引发莱姆关节炎。

Macrophages exposed to Borrelia burgdorferi induce Lyme arthritis in hamsters.

作者信息

Du Chateau B K, England D M, Callister S M, Lim L C, Lovrich S D, Schell R F

机构信息

Wisconsin State Laboratory of Hygiene, Madison, Wisconsin 53706, USA.

出版信息

Infect Immun. 1996 Jul;64(7):2540-7. doi: 10.1128/iai.64.7.2540-2547.1996.

Abstract

The mechanism(s) by which Lyme arthritis is induced has not been elucidated. In this study, we showed that macrophages have a direct, effector role in the pathogenesis of Lyme arthritis. Severe destructive arthritis was induced in recipients of macrophages obtained from Borrelia burgdorferi-vaccinated and nonvaccinated hamsters exposed to Formalin-inactivated B. burgdorferi in vitro and then challenged with the Lyme spirochete. Swelling of the hind paws was detected within 8 h of infection, increased rapidly, and peaked at 21 h. This initial swelling decreased, and by day 4 only slight swelling was detected. Severe swelling of the hind paws was detected 8 days after infection and increased rapidly, with peak swelling occurring on day 11. Histopathologic examination affirmed that macrophages exposed to Formalin-inactivated spirochetes induced a severe destructive Lyme arthritis. The onset and severity of the severe destructive arthritis were dependent on the number of macrophages transferred. By contrast, macrophages not exposed to Formalin-inactivated B. burgdorferi failed to induce severe destructive arthritis in recipients after challenge with B. burgdorferi. Similarly, severe destructive arthritis was not detected in recipients of macrophages injected with spirochetal growth medium. Our results also showed that transferred macrophages could not protect hamsters from infection with B. burgdorferi, as spirochetes were readily recovered from their tissues when cultured. These findings demonstrate that macrophages exposed to B. burgdorferi are directly involved in the induction of Lyme arthritis.

摘要

莱姆关节炎的诱发机制尚未阐明。在本研究中,我们表明巨噬细胞在莱姆关节炎的发病机制中具有直接的效应作用。从接种过伯氏疏螺旋体疫苗和未接种过疫苗的仓鼠体内获取巨噬细胞,将其在体外暴露于福尔马林灭活的伯氏疏螺旋体,然后用莱姆螺旋体进行攻击,结果在受体动物中诱发了严重的破坏性关节炎。感染后8小时内即可检测到后爪肿胀,肿胀迅速加剧,并在21小时达到峰值。最初的肿胀随后减轻,到第4天时仅检测到轻微肿胀。感染后8天检测到后爪严重肿胀,且迅速加重,肿胀峰值出现在第11天。组织病理学检查证实,暴露于福尔马林灭活螺旋体的巨噬细胞可诱发严重的破坏性莱姆关节炎。严重破坏性关节炎的发作和严重程度取决于转移的巨噬细胞数量。相比之下,未暴露于福尔马林灭活伯氏疏螺旋体的巨噬细胞在受到伯氏疏螺旋体攻击后,未能在受体动物中诱发严重的破坏性关节炎。同样,在注射螺旋体生长培养基的巨噬细胞受体中未检测到严重的破坏性关节炎。我们的结果还表明,转移的巨噬细胞不能保护仓鼠免受伯氏疏螺旋体感染,因为在培养时很容易从它们的组织中分离出螺旋体。这些发现表明,暴露于伯氏疏螺旋体的巨噬细胞直接参与了莱姆关节炎的诱发过程。

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