Holten-Andersen L, Doherty T M, Korsholm K S, Andersen P
Department of Infectious Disease Immunology, Statens Serum Institut, DK-2300 Copenhagen, Denmark.
Infect Immun. 2004 Mar;72(3):1608-17. doi: 10.1128/IAI.72.3.1608-1617.2004.
Recombinant, immunodominant antigens derived from Mycobacterium tuberculosis can be used to effectively vaccinate against subsequent infection. However, the efficacy of these recombinant proteins is dependent on the adjuvant used for their delivery. This problem affects many potential vaccines, not just those for tuberculosis, so the discovery of adjuvants that can promote the development of cell-mediated immunity is of great interest. We have previously shown that the combination of the cationic surfactant dimethyl dioctadecyl ammonium bromide and the immunomodulator modified lipid A synergistically potentiates Th1 T-cell responses. Here we report a screening program for other adjuvants with reported Th1-promoting activity and identify a second novel adjuvant formulation that drives the development of Th1 responses with an extremely high efficacy. The combination of dimethyl dioctadecyl ammonium bromide and the synthetic cord factor trehalose dibehenate promotes strong protective immune responses, without overt toxicity, against M. tuberculosis infection in a vaccination model and thus appears to be a very promising candidate for the development of human vaccines.
源自结核分枝杆菌的重组免疫显性抗原可用于有效预防后续感染。然而,这些重组蛋白的功效取决于用于递送它们的佐剂。这个问题影响了许多潜在疫苗,而不仅仅是结核病疫苗,因此能够促进细胞介导免疫发展的佐剂的发现备受关注。我们之前已经表明,阳离子表面活性剂二甲基二十八烷基溴化铵和免疫调节剂修饰的脂质A协同增强Th1 T细胞反应。在此,我们报告了一个针对其他具有Th1促进活性的佐剂的筛选计划,并确定了第二种新型佐剂配方,该配方能以极高的功效驱动Th1反应的发展。在疫苗接种模型中,二甲基二十八烷基溴化铵与合成的索状因子二山嵛酸海藻糖的组合可促进针对结核分枝杆菌感染的强大保护性免疫反应,且无明显毒性,因此似乎是开发人类疫苗的非常有前景的候选物。