Pinto Eduardo Fonseca, de Mello Cortezia Marcelle, Rossi-Bergmann Bartira
Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, 21.949-900 Rio de Janeiro, Brazil.
Vaccine. 2003 Sep 8;21(25-26):3534-41. doi: 10.1016/s0264-410x(03)00427-4.
The induction of oral tolerance against disease-inducing antigens has emerged as a feasible strategy to prevent immunopathologies. In this study, we investigated the effect of oral immunization with whole antigens of Leishmania amazonensis promastigotes (LaAg) on murine cutaneous leishmaniasis. We found that two oral doses with 100 microg LaAg rendered BALB/c and C57BL/6 mice more resistant against subsequent infection with L. amazonensis. The oral vaccine also partially protected BALB/c mice against Leishmania major infection. Unlike the oral route, hepatic immunization was without effect, indicating a requirement for antigen passage through the gut mucosa. Oral LaAg significantly impaired the capacity of infected BALB/c mice to mount a disease-associated hypersensitivity response, compatible with peripheral tolerization. Both IFN-gamma and IL-10, but not IL-4 were greatly elevated in the mesenteric lymph nodes whereas only IFN-gamma was increased in the peripheral lymph nodes, compatible with a TH1 cytokine response. Gamma delta TCR+ T cells may be an important component in antigenic sensitization of the gut mucosa since their depletion during oral immunization reverted protection. These results demonstrate for the first time the feasibility of using the oral route of immunization to induce protection against cutaneous leishmaniasis using a crude parasite antigen.
诱导针对致病抗原的口服耐受性已成为预防免疫病理的一种可行策略。在本研究中,我们调查了用亚马逊利什曼原虫前鞭毛体全抗原(LaAg)进行口服免疫对小鼠皮肤利什曼病的影响。我们发现,用100微克LaAg进行两次口服给药可使BALB/c和C57BL/6小鼠对随后的亚马逊利什曼原虫感染更具抵抗力。口服疫苗也部分保护BALB/c小鼠免受硕大利什曼原虫感染。与口服途径不同,肝脏免疫无效,这表明抗原需要通过肠道黏膜。口服LaAg显著损害了感染的BALB/c小鼠引发与疾病相关的超敏反应的能力,这与外周耐受相符。肠系膜淋巴结中IFN-γ和IL-10均大幅升高,但IL-4未升高,而外周淋巴结中仅IFN-γ升高,这与TH1细胞因子反应相符。γδTCR+T细胞可能是肠道黏膜抗原致敏的重要组成部分,因为在口服免疫期间它们的耗竭会使保护作用逆转。这些结果首次证明了使用口服免疫途径,利用粗制寄生虫抗原诱导针对皮肤利什曼病的保护作用的可行性。