Li Q X, Camerini D, Kuritzkes D R, Chen I S
Department of Microbiology and Immunology, UCLA School of Medicine 90095, USA.
Virology. 1995 Dec 20;214(2):680-4. doi: 10.1006/viro.1995.0085.
Recombinant human T-cell leukemia virus type II (HTLV-II) envelope external glycoprotein, gp46-II, was expressed using a vaccinia virus vector. A recombinant gp46-II fused to an epitope of the influenza virus hemagglutinin, YPYDVPDYA, was purified by immunoaffinity chromatography. The purified glycoprotein was used to immunize Balb/c mice, and antibodies against gp46-II were detected by Western blot analysis and syncytium inhibition assays. We transformed spleen cells from the immunized mice by retroviral infection with ABL-MYC (psi 2) and intraperitoneally transplanted the infected cells into syngeneic Balb/c and severe combined immunodeficient (SCID) mice. The plasmacytomas established ascitic tumors that produced antibodies directed against HTLV-II gp46-II. Ascites developed more rapidly in SCID mice than in normal syngeneic mice. This procedure provides a general means to generate antibodies rapidly.
使用痘苗病毒载体表达重组人II型T细胞白血病病毒(HTLV-II)包膜外糖蛋白gp46-II。通过免疫亲和层析纯化与流感病毒血凝素表位YPYDVPDYA融合的重组gp46-II。用纯化的糖蛋白免疫Balb/c小鼠,并通过蛋白质免疫印迹分析和细胞融合抑制试验检测抗gp46-II的抗体。我们用ABL-MYC(psi 2)逆转录病毒感染免疫小鼠的脾细胞,并将感染的细胞腹腔移植到同基因Balb/c小鼠和严重联合免疫缺陷(SCID)小鼠体内。所建立的浆细胞瘤形成了产生抗HTLV-II gp46-II抗体的腹水瘤。SCID小鼠比正常同基因小鼠腹水形成得更快。该方法提供了一种快速产生抗体的通用手段。