Isaka Masanori, Yasuda Yoko, Taniguchi Tooru, Kozuka Satoshi, Matano Keiko, Maeyama Jun-ichi, Morokuma Kazunori, Ohkuma Kunio, Goto Norihisa, Tochikubo Kunio
Department of Microbiology, Nagoya City University Medical School, Mizuho-ku, Nagoya 467-8601, Japan.
Vaccine. 2003 Mar 7;21(11-12):1165-73. doi: 10.1016/s0264-410x(02)00516-9.
To investigate the possibility of intranasal immunization with an acellular pertussis vaccine, groups of mice were administered intranasally with aluminium-non-adsorbed pertussis toxoid (PTd; 0.5 or 5 microg) and formalin-treated filamentous hemagglutinin (fFHA; 5 microg) with and without recombinant cholera toxin B subunit (rCTB; 10 microg) as a mucosal adjuvant. At a low concentration of PTd, the following things became clear: (1) earlier and higher elevation of serum anti-PTd and anti-FHA IgG antibody titres in the presence of rCTB than in its absence, (2) higher serum anti-PTd and anti-FHA IgG antibody titres than 200 and 100 ELISA units ml(-1) (EU ml(-1)) in all mice, respectively, in the presence of rCTB, which were obtained by calibration against a reference anti-pertussis mouse serum, and (3) in an intranasal challenge experiment with Bordetella pertussis, slightly more rapid elimination of the bacteria from the lungs of mice intranasally immunized in the presence of rCTB, suggesting the effectiveness of rCTB as a mucosal adjuvant. However, irrespective of rCTB and dose of PTd, mice which were immunized four times and sacrificed on day 35 developed high levels of anti-PTd serum IgG antibodies, high or moderate levels of anti-FHA serum IgG antibodies and mucosal anti-PTd IgA antibodies in the lungs; only a slight or no increase of anti-FHA mucosal IgA antibodies was observed in the lung. These facts suggested the immunogenicity and mucosal adjuvanticity of PTd, and therefore, the mucosal adjuvanticity of rCTB seemed to be inconspicuous. Moreover, the addition of rCTB induced higher anti-PTd serum IgE antibody responses than no addition of it depending on dose of PTd. These results show that dose of PTd included in an acellular pertussis vaccine had better be low as possible and the addition of rCTB may not be always necessary in case of this nasal vaccine alone unlike tetanus and diphtheria toxoids and hepatitis B virus vaccine reported before.
为研究无细胞百日咳疫苗鼻内免疫的可能性,将小鼠分组,经鼻给予铝未吸附的百日咳类毒素(PTd;0.5或5微克)和经福尔马林处理的丝状血凝素(fFHA;5微克),同时或不同时添加重组霍乱毒素B亚单位(rCTB;10微克)作为黏膜佐剂。在PTd低浓度时,以下情况变得清晰:(1)存在rCTB时血清抗PTd和抗FHA IgG抗体滴度比不存在时升高更早且更高;(2)存在rCTB时,所有小鼠血清抗PTd和抗FHA IgG抗体滴度分别高于200和100酶联免疫吸附测定单位每毫升(EU/ml),这是通过与参考抗百日咳小鼠血清校准获得的;(3)在百日咳博德特氏菌鼻内攻击实验中,存在rCTB时经鼻免疫小鼠肺中细菌的清除略快,表明rCTB作为黏膜佐剂有效。然而,无论rCTB和PTd剂量如何,免疫4次并在第35天处死的小鼠血清中产生了高水平的抗PTd IgG抗体、高水平或中等水平的抗FHA血清IgG抗体以及肺中的黏膜抗PTd IgA抗体;在肺中仅观察到抗FHA黏膜IgA抗体略有增加或未增加。这些事实表明了PTd的免疫原性和黏膜佐剂性,因此,rCTB的黏膜佐剂性似乎不明显。此外,根据PTd剂量,添加rCTB比不添加诱导更高的抗PTd血清IgE抗体反应。这些结果表明,无细胞百日咳疫苗中所含PTd的剂量最好尽可能低,并且与之前报道的破伤风类毒素、白喉类毒素和乙肝病毒疫苗不同,仅就这种鼻用疫苗而言,添加rCTB可能并非总是必要的。