Courtney Amy N, Nehete Pramod N, Nehete Bharti P, Thapa Prakash, Zhou Dapeng, Sastry K Jagannadha
Department of Immunology, Unit 901, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Vaccine. 2009 May 26;27(25-26):3335-41. doi: 10.1016/j.vaccine.2009.01.083. Epub 2009 Feb 5.
Mucosal delivery of vaccines against sexually transmitted pathogens is important to elicit strong immune responses at biologically relevant sites. However, inclusion of appropriate adjuvants is essential to overcome the inherent mucosal tolerance. We present evidence in support of the effectiveness of co-administering alpha-galactosylceramide (alpha-GalCer) as an adjuvant with a CTL-inducing HIV envelope peptide, via either oral or intranasal route, to prime antigen-specific immune responses in multiple systemic and mucosal compartments. Contrary to the known potential of repeated parenteral dosing with alpha-GalCer to induce NKT cell anergy that could compromise adoptive immunity development, we have observed that two and three doses delivered by the intranasal or oral route were more efficient in priming broader antigen-specific immune responses. These results demonstrate the effectiveness of alpha-GalCer as adjuvant for repeated intranasal or oral administration of vaccines for protection against mucosally transmitted pathogens.
通过粘膜递送针对性传播病原体的疫苗对于在生物学相关部位引发强烈免疫反应很重要。然而,加入合适的佐剂对于克服固有的粘膜耐受性至关重要。我们提供的证据支持,通过口服或鼻内途径将α-半乳糖神经酰胺(α-GalCer)作为佐剂与诱导CTL的HIV包膜肽共同给药,可在多个全身和粘膜区室引发抗原特异性免疫反应。与已知的通过重复肠胃外给药α-GalCer诱导NKT细胞无反应性从而可能损害过继免疫发展的可能性相反,我们观察到通过鼻内或口服途径给予两剂和三剂在引发更广泛的抗原特异性免疫反应方面更有效。这些结果证明了α-GalCer作为佐剂用于重复鼻内或口服疫苗接种以预防粘膜传播病原体的有效性。