Gürsel M, Tunca S, Ozkan M, Ozcengiz G, Alaeddinoglu G
Department of Biological Sciences, Middle East Technical University, Ankara, Turkey.
Vaccine. 1999 Mar 17;17(11-12):1376-83. doi: 10.1016/s0264-410x(98)00383-1.
Bacterial DNA and oligodeoxynucleotides containing immunostimulatory sequences with a CpG motif stimulated a Th1 type response in vivo. The adjuvant action of a non-coding plasmid DNA derived from pRc/CMV HBS (encoding the S region of hepatitis B surface antigen, HBsAg) in mice was investigated. The role of methylation on the adjuvanticity of the plasmid as well as the effect of vaccine formulation employed on the outcome of antigen-specific humoral and cellular responses were also studied. The results demonstrated that plasmid DNA acted as a Th1 promoting adjuvant when mixed as such or co-entrapped in liposomes with a very low dose of antigen. However, the adjuvant activity was lost when separate liposome entrapped formulations of both the antigen and the plasmid DNA were mixed, indicating a necessity for the antigen and the plasmid DNA to contact the same APC for optimal immune activation. A decreased adjuvanticity of plasmid DNA upon methylation with HpaII methyltransferase was also demonstrated. A mechanism that may help partially explain the reduction in adjuvanticity after modification of C residues is also discussed.
含有具有CpG基序的免疫刺激序列的细菌DNA和寡脱氧核苷酸在体内刺激了Th1型反应。研究了源自pRc/CMV HBS(编码乙肝表面抗原HBsAg的S区)的非编码质粒DNA在小鼠中的佐剂作用。还研究了甲基化对质粒佐剂活性的作用以及所采用的疫苗制剂对抗抗原特异性体液和细胞反应结果的影响。结果表明,质粒DNA单独混合或与极低剂量抗原共包封于脂质体中时,可作为促进Th1的佐剂。然而,当抗原和质粒DNA分别包封于脂质体的制剂混合时,佐剂活性丧失,这表明抗原和质粒DNA需要接触同一抗原呈递细胞以实现最佳免疫激活。还证明了用HpaII甲基转移酶甲基化后质粒DNA的佐剂活性降低。还讨论了一种可能有助于部分解释C残基修饰后佐剂活性降低的机制。