Rydell Niclas, Sjöholm Ingvar
Department of Pharmacy, Division of Pharmaceutics, University of Uppsala, P.O. Box 580, SE-75123 Uppsala, Sweden.
Vaccine. 2004 Mar 12;22(9-10):1265-74. doi: 10.1016/j.vaccine.2003.09.034.
Oral vaccination offers the advantage of eliciting both a mucosal and a systemic immune response. This study investigated the use of polyacryl starch microparticles as adjuvant for oral vaccination against diphtheria. Diphtheria toxin or cross-reacting material (CRM197) were covalently conjugated to the microparticles and fed to mice by oral gavage. Investigation of formaldehyde treatment as a means of either detoxifying (diphtheria toxin) or stabilising (CRM197) these formulations were also made. We show that all our formulations given orally or parenterally to mice induced a strong systemic immune response. Only formulations given orally induced a mucosal IgA-response. Furthermore, our formulations given parenterally or orally induced a strong diphtheria toxin-neutralising antibody response.
口服疫苗接种具有引发黏膜免疫反应和全身免疫反应的优势。本研究调查了聚丙烯淀粉微粒作为口服白喉疫苗佐剂的用途。将白喉毒素或交叉反应物质(CRM197)共价偶联到微粒上,并通过灌胃法喂给小鼠。还研究了甲醛处理作为使这些制剂解毒(白喉毒素)或稳定(CRM197)的手段。我们发现,给小鼠口服或注射我们所有的制剂均能诱导强烈的全身免疫反应。只有口服制剂能诱导黏膜IgA反应。此外,我们注射或口服的制剂能诱导强烈的白喉毒素中和抗体反应。