Cheevers W P, Knowles D P, McGuire T C, Baszler T V, Hullinger G A
Department of Veterinary Microbiology, Washington State University, Pullman 99164.
Vet Immunol Immunopathol. 1994 Sep;42(3-4):237-51. doi: 10.1016/0165-2427(94)90070-1.
This study evaluated infection and disease following caprine arthritis-encephalitis lentivirus (CAEV) challenge of goats with existent immune response to CAEV surface and transmembrane envelope glycoproteins. Six Saanen goats were vaccinated three times with recombinant vaccinia virus rWR63 expressing glycoproteins encoded by the CAEV-63 envelope gene. Two goats were immunized with rWRSC11, a control vaccinia virus derived from the pSC11 vaccinia expression plasmid without the CAEV envelope gene. One pair of rWR63 vaccinated goats received a booster immunization with recombinant surface glycoprotein in Freund's complete adjuvant, a second pair was boosted by intravenous inoculation with rWR63, and the third pair was boosted by immunization with HPLC purified native CAEV surface glycoprotein in Freund's complete adjuvant. All six goats vaccinated with rWR63 developed antibody responses to CAEV envelope glycoproteins; however, CAEV-63 neutralizing antibody was not detected. Neither of the rWRSC11-vaccinated goats developed CAEV reactive antibody. All goats were challenged by intravenous inoculation with 10(6) TCID50 CAEV-63. All goats became infected following challenge infection, shown by detection of serum antibody to CAEV core proteins and virus isolation. Existent CAEV-63 immune responses did not detectably alter the severity of inflammatory joint lesions at 24 weeks postchallenge.
本研究评估了对山羊关节炎-脑炎慢病毒(CAEV)表面和跨膜包膜糖蛋白已有免疫反应的山羊在受到CAEV攻击后的感染和疾病情况。六只萨能山羊用表达由CAEV-63包膜基因编码的糖蛋白的重组痘苗病毒rWR63进行了三次接种。两只山羊用rWRSC11进行免疫,rWRSC11是一种源自pSC11痘苗表达质粒且无CAEV包膜基因的对照痘苗病毒。一对接种rWR63的山羊用弗氏完全佐剂中的重组表面糖蛋白进行加强免疫,第二对通过静脉接种rWR63进行加强,第三对用HPLC纯化的天然CAEV表面糖蛋白在弗氏完全佐剂中进行加强免疫。所有六只接种rWR63的山羊都产生了针对CAEV包膜糖蛋白的抗体反应;然而,未检测到CAEV-63中和抗体。接种rWRSC11的两只山羊均未产生CAEV反应性抗体。所有山羊通过静脉接种10(6) TCID50 CAEV-63进行攻击。攻击感染后所有山羊均被感染,这通过检测针对CAEV核心蛋白的血清抗体和病毒分离得以证实。在攻击后24周时,已有的CAEV-63免疫反应未显著改变炎性关节损伤的严重程度。