Blanchard T G, Lycke N, Czinn S J, Nedrud J G
Institute of Pathology, Case Western Reserve University, Cleveland, OH 44106-4943, USA.
Immunology. 1998 May;94(1):22-7. doi: 10.1046/j.1365-2567.1998.00482.x.
Cholera toxin is a potent oral mucosal adjuvant for enteric immunization. Several studies suggest that commercial cholera toxin B subunit (cCTB; purified from holotoxin) may be an effective non-toxic alternative for oral immunization. The present study was performed, using an infectious disease model, to determine if the oral mucosal adjuvanticity of CTB is dependent on contaminating holotoxin. Mice were orally immunized with Helicobacter felis sonicate and either cholera holotoxin, cCTB or recombinant cholera toxin B subunit (rCTB). Serum immunoglobulin G (IgG) and intestinal immunoglobulin A (IgA) antibody responses were determined and the mice were challenged with live H. felis to determine the degree of protective immunity induced. All orally immunized mice responded with serum IgG antibody titres regardless of the adjuvant used. However, only mice immunized with either holotoxin or the cCTB responded with an intestinal mucosal IgA response. Consistent with the production of mucosal antibodies, mice immunized with either holotoxin or cCTB as adjuvants were protected from challenge while mice receiving H. felis sonicate and rCTB all became infected. cCTB induced the accumulation of cAMP in mouse thymocytes at a level equal to 0.1% of that induced by holotoxin, whereas rCTB was devoid of any activity. These results indicate that CTB possesses no intrinsic mucosal adjuvant activity when administered orally. Therefore, when used as an oral adjuvant, CTB should also include small, non-toxic doses of cholera toxin.
霍乱毒素是用于肠道免疫的一种强效口服黏膜佐剂。多项研究表明,商业霍乱毒素B亚基(cCTB;从全毒素中纯化)可能是口服免疫的一种有效的无毒替代品。本研究利用一种传染病模型来确定CTB的口服黏膜佐剂活性是否依赖于污染的全毒素。用猫螺杆菌超声裂解物以及霍乱全毒素、cCTB或重组霍乱毒素B亚基(rCTB)对小鼠进行口服免疫。测定血清免疫球蛋白G(IgG)和肠道免疫球蛋白A(IgA)抗体反应,并对小鼠用活的猫螺杆菌进行攻击以确定诱导的保护性免疫程度。所有口服免疫的小鼠无论使用何种佐剂均产生血清IgG抗体滴度。然而,只有用全毒素或cCTB免疫的小鼠产生肠道黏膜IgA反应。与黏膜抗体的产生一致,用全毒素或cCTB作为佐剂免疫的小鼠受到保护而免受攻击,而接受猫螺杆菌超声裂解物和rCTB的小鼠均被感染。cCTB在小鼠胸腺细胞中诱导的cAMP积累水平相当于全毒素诱导水平的0.1%,而rCTB则没有任何活性。这些结果表明,口服给药时CTB不具有内在的黏膜佐剂活性。因此,当用作口服佐剂时,CTB还应包含小剂量无毒的霍乱毒素。