Cheevers W P, Knowles D P, Norton L K
Department of Veterinary Microbiology and Pathology, Washington State University, Pullman 99164-7040.
J Infect Dis. 1991 Oct;164(4):679-85. doi: 10.1093/infdis/164.4.679.
Fifteen newborn Saanen goats were orally infected with a biologically cloned isolate of caprine arthritis-encephalitis virus (CAEV-63). At 33.5 months after infection, 8 of 12 seropositive goats had CAEV-63-specific neutralizing antibody. Five neutralization-positive goats developed clinically apparent arthritis of carpal joints, three of which had periarticular swelling indicating severe synovitis. Arthritis was not evident in age-matched controls or infected goats without neutralizing antibody. Multiple viral isolates were obtained from synovial fluid or synovial fluid cells of arthritic joints between 36.4 and 44.9 months after infection, and successive isolates from individual joints were defined as antigenic variants expressing type-specific neutralization epitopes. Thus, the evolution of neutralizing antibody does not arrest viral replication or development of progressive inflammatory lesions. Rather, some antigenic variants produced in the presence of neutralizing antibody are clonally expanded within carpal joints, and severe joint inflammation is specifically associated with these variants.
15只新生的萨能山羊经口感染了山羊关节炎-脑炎病毒(CAEV-63)的生物克隆分离株。感染后33.5个月,12只血清阳性山羊中有8只具有CAEV-63特异性中和抗体。5只中和阳性山羊出现了明显的腕关节关节炎,其中3只有关节周围肿胀,表明有严重的滑膜炎。在年龄匹配的对照山羊或无中和抗体的感染山羊中未发现关节炎。在感染后36.4至44.9个月之间,从关节炎关节的滑液或滑液细胞中获得了多个病毒分离株,来自单个关节的连续分离株被定义为表达型特异性中和表位的抗原变异体。因此,中和抗体的产生并不能阻止病毒复制或进展性炎症病变的发展。相反,一些在中和抗体存在下产生的抗原变异体在腕关节内克隆性扩增,严重的关节炎症与这些变异体密切相关。