Jespersgaard C, Zhang P, Hajishengallis G, Russell M W, Michalek S M
Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
Infect Immun. 2001 Nov;69(11):6604-11. doi: 10.1128/IAI.69.11.6604-6611.2001.
Attenuated Salmonella enterica serovar Typhimurium has been used for targeted delivery of recombinant antigens to gut- and nose-associated lymphoid tissues. Contradictory reports have described the effect of preexisting immunity to the antigen delivery vehicle. We decided to examine this discrepancy by studying the effect of immunizing mice by the intranasal (i.n.) route with Salmonella expressing an insoluble protein and to study the ability to augment recall responses by boosting with either Salmonella-expressed protein or purified soluble protein alone. The glucan-binding domain (GLU) of the enzyme glucosyltransferase (GTF), which is an important virulence factor of Streptococcus mutans, was recombinantly expressed in the insoluble phase in S. enterica serovar Typhimurium, and the immunogenicity of this construct was studied in mice. We examined the induction of primary immune responses by insoluble GLU polypeptide delivered in Salmonella at week 1 (groups 1 and 2) and recall responses after a week 15 boost with either Salmonella expressing GLU (group 1) or purified GLU polypeptide (groups 2 and 3). Group 4 served as the control and received phosphate-buffered saline alone by the i.n. route. Significant anti-GLU serum immunoglobulin G (IgG) levels were seen in groups 1, 2, and 3 at week 18 (P < 0.001), i.e., 3 weeks after the booster immunization. Mice in group 2, who received Salmonella followed by GLU, had the highest GLU-specific IgG levels among all groups. The serum IgG levels persisted in all responding groups for at least 7 weeks after the boost (week 22). The IgG2a/IgG1 subclass ratio of serum anti-GLU antibodies in group 1 significantly increased after the boost. These results support the induction of a type 1-like immune response to GLU after primary and booster immunizations with Salmonella expressing GLU. On the other hand, group 2 mice, which received Salmonella expressing GLU as the primary dose and soluble protein as the booster dose, exhibited a shift from a type 1-like to a more type 2-like immune response to GLU following the boost. These results indicate that S. enterica serovar Typhimurium is an excellent delivery vehicle for the insoluble and recombinantly expressed GLU of GTF and that this construct was especially effective in priming the host for a secondary response to soluble GLU polypeptide.
减毒鼠伤寒沙门氏菌已被用于将重组抗原靶向递送至肠道和鼻相关淋巴组织。关于对抗原递送载体的预先存在的免疫的影响,已有相互矛盾的报道。我们决定通过研究经鼻内(i.n.)途径用表达不溶性蛋白质的沙门氏菌免疫小鼠的效果,并研究单独用沙门氏菌表达的蛋白质或纯化的可溶性蛋白质加强免疫以增强回忆反应的能力,来检验这种差异。变形链球菌的一种重要毒力因子葡糖基转移酶(GTF)的葡聚糖结合结构域(GLU)在鼠伤寒沙门氏菌的不溶性相中进行了重组表达,并在小鼠中研究了该构建体的免疫原性。我们在第1周(第1组和第2组)检测了经沙门氏菌递送的不溶性GLU多肽诱导的初次免疫反应,以及在第15周用表达GLU的沙门氏菌(第1组)或纯化的GLU多肽(第2组和第3组)加强免疫后的回忆反应。第4组作为对照,经鼻内途径仅接受磷酸盐缓冲盐水。在加强免疫后3周即第18周时,第1、2和3组中均检测到显著的抗GLU血清免疫球蛋白G(IgG)水平(P<0.001)。接受沙门氏菌后再接受GLU的第2组小鼠在所有组中具有最高的GLU特异性IgG水平。加强免疫后,所有反应组中的血清IgG水平在至少7周内(第22周)持续存在。加强免疫后,第1组血清抗GLU抗体的IgG2a/IgG1亚类比值显著增加。这些结果支持在用表达GLU的沙门氏菌进行初次和加强免疫后,对GLU诱导出1型样免疫反应。另一方面,第2组小鼠接受表达GLU的沙门氏菌作为初免剂量,可溶性蛋白质作为加强剂量,加强免疫后对GLU的免疫反应从1型样转变为更偏向2型样。这些结果表明,鼠伤寒沙门氏菌是GTF的不溶性且重组表达的GLU的优良递送载体,并且该构建体在使宿主对可溶性GLU多肽产生二次反应的初次免疫中特别有效。