Asakura Y, Lundholm P, Kjerrström A, Benthin R, Lucht E, Fukushima J, Schwartz S, Okuda K, Wahren B, Hinkula J
Swedish Institute for Infectious Disease Control, Microbiology and Tumorbiology Center, Karolinska Institute, Stockholm.
Biol Chem. 1999 Mar;380(3):375-9. doi: 10.1515/BC.1999.049.
DNA-based immunization has been shown to induce protective immunity against several microbial pathogens including HIV-1. Several routes of DNA vaccination have been exploited. However, the properties of the immune responses seem to differ with the different routes used for DNA delivery, ultimately affecting the outcome of experimental challenge. We measured the primary immune response following one vaccination. This report presents differences associated with three different DNA delivery routes: intramuscular injection, intranasal application, and gene-gun based immunization. Induction of systemic humoral immune responses was achieved most efficiently by either intranasal or gene-gun mediated immunization, followed by intramuscular injection. Mucosal IgA was reproducibly induced by intranasal instillation of the DNA, and found in lung washings, faeces, and vaginal washings. Cytotoxic T cells were not induced by a single immunization, but were observed after three immunizations using intramuscular injections.
基于DNA的免疫接种已被证明可诱导针对包括HIV-1在内的多种微生物病原体的保护性免疫。人们已经探索了几种DNA疫苗接种途径。然而,免疫反应的特性似乎因用于DNA递送的不同途径而有所不同,最终影响实验性攻击的结果。我们测量了一次接种后的初次免疫反应。本报告介绍了与三种不同DNA递送途径相关的差异:肌肉注射、鼻内给药和基于基因枪的免疫接种。通过鼻内或基因枪介导的免疫接种,最有效地诱导了全身性体液免疫反应,其次是肌肉注射。通过鼻内滴注DNA可重复性地诱导黏膜IgA,并在肺灌洗物、粪便和阴道灌洗物中发现。单次免疫接种不会诱导细胞毒性T细胞,但在使用肌肉注射进行三次免疫接种后可观察到。