Thibodeau L, Tremblay C, Lachapelle L
Institut Armand-Frappier, Université du Québec, Laval, Canada.
C R Acad Sci III. 1991;313(9):389-94.
Given the sexual transmission of HIV, the establishment of a genital mucosal immunity through secretory IgA may be necessary to achieve protection. We have investigated if repeated stimulations of oral mucosa with HIV-Immunosomes would lead to the production of secretory IgA in saliva and also, if such an oral immunization could prime the immune system to an early systemic immune response following a parenteral immunisation with a low dose of the antigen. HIV-1 gp 160-specific secretory IgA were detected in the saliva of all rabbits orally immunized with HIV-Immunosomes. As early as one week after the parenteral immunization, high titers of serum IgA, IgM and IgG were detected both in mice and rabbits that had been orally stimulated with the antigen. These antibodies could neutralize HIV infectivity in vitro. Animals that were immunized only parenterally showed a very weak humoral immune response.
鉴于HIV的性传播途径,通过分泌型IgA建立生殖器黏膜免疫对于实现保护作用可能是必要的。我们研究了用HIV免疫小体反复刺激口腔黏膜是否会导致唾液中分泌型IgA的产生,以及这种口服免疫是否能使免疫系统在低剂量抗原的肠胃外免疫后引发早期全身免疫反应。在用HIV免疫小体进行口服免疫的所有兔子的唾液中均检测到了HIV-1 gp 160特异性分泌型IgA。在肠胃外免疫后仅一周,在用抗原进行口服刺激的小鼠和兔子中均检测到了高滴度的血清IgA、IgM和IgG。这些抗体在体外能够中和HIV的感染性。仅接受肠胃外免疫的动物表现出非常微弱的体液免疫反应。