Kusumoto Y, Ogawa T, Hamada S
Department of Oral Microbiology, Faculty of Dentistry, Osaka University, Japan.
Arch Oral Biol. 1993 May;38(5):361-7. doi: 10.1016/0003-9969(93)90206-2.
The humoral immune response and induction of antigen-specific antibody-secreting cells in mucosal lymphoid tissues were examined in mice immunized subcutaneously or orally with fimbrial protein purified from Porphyromonas gingivalis strain 381. A group of BALB/c mice was immunized subcutaneously with P. gingivalis fimbriae and semisynthetic adjuvant GM-53 in Freund's incomplete adjuvant on days 0 and 28. Another group of mice was immunized perorally with liposome containing fimbriae and GM-53 on days 0, 1, 27 and 28. In the mice immunized subcutaneously, salivary anti-fimbrial IgM antibodies were detected transiently on day 5, followed by the appearance of specific IgG and IgA antibodies on day 14. Higher concentrations of salivary IgG and IgA anti-fimbrial antibodies were found after the second immunization. Fimbria-specific IgM and IgG spot-forming cells (SFC) were detected in cervical lymph nodes of the immunized mice by the ELISPOT method. Fimbria-specific IgA SFC but not IgM and IgG appeared in the parotid and submandibular glands of subcutaneously immunized mice. On the other hand, mice immunized by gastric intubation generated almost exclusively salivary anti-fimbrial IgA antibodies. In agreement with this finding, increased numbers of antigen-specific IgA but not IgM and IgG SFC were seen in parotid and submandibular glands, but not in cervical lymph nodes of orally immunized mice. It can be concluded that systemic or oral immunization with fimbrial antigen induces distinct immune responses in specific lymphoid tissues or in the salivary glands in respect of their temporal sequences and the numbers of plasma cells secreting antigen-specific and non-specific immunoglobulins.
在用从牙龈卟啉单胞菌381菌株纯化的菌毛蛋白对小鼠进行皮下或口服免疫后,检测了其体液免疫反应以及黏膜淋巴组织中抗原特异性抗体分泌细胞的诱导情况。一组BALB/c小鼠在第0天和第28天用牙龈卟啉单胞菌菌毛和半合成佐剂GM-53于弗氏不完全佐剂中进行皮下免疫。另一组小鼠在第0天、第1天、第27天和第28天口服含菌毛和GM-53的脂质体。在皮下免疫的小鼠中,第5天短暂检测到唾液抗菌毛IgM抗体,随后在第14天出现特异性IgG和IgA抗体。第二次免疫后发现唾液中IgG和IgA抗菌毛抗体浓度更高。通过ELISPOT法在免疫小鼠的颈部淋巴结中检测到菌毛特异性IgM和IgG斑点形成细胞(SFC)。在皮下免疫小鼠的腮腺和颌下腺中出现了菌毛特异性IgA SFC,但未出现IgM和IgG。另一方面,经胃插管免疫的小鼠几乎只产生唾液抗菌毛IgA抗体。与此发现一致,在口服免疫小鼠的腮腺和颌下腺中可见抗原特异性IgA而非IgM和IgG SFC数量增加,但在颈部淋巴结中未增加。可以得出结论,用菌毛抗原进行全身或口服免疫在特定淋巴组织或唾液腺中诱导出不同的免疫反应,这体现在其时间顺序以及分泌抗原特异性和非特异性免疫球蛋白的浆细胞数量上。