Steffen M J, Ebersole J L
Department of Periodontics, University of Texas Health Science Center, San Antonio 78284.
Infect Immun. 1992 Feb;60(2):337-44. doi: 10.1128/iai.60.2.337-344.1992.
Formalinized Mycoplasma pulmonis, along with aluminum hydroxide as an adjuvant, was used to subcutaneously immunize rats in the vicinity of the salivary gland to examine the characteristics of the secretory immune response to this pathogen. The induction of specific antibody to this microorganism was detected in serum and the exocrine fluids, namely, saliva and lung lavage fluid. Both immunoglobulin G (IgG) and IgA isotype antibodies were detected in each of these fluids after primary and secondary local immunizations. Serum responses from immunized animals were significantly greater than in the control group, but a dose response was not observed in either IgG or IgA antibody at the dosages selected for immunization. Salivary IgG antibody responses peaked early after both the primary and secondary immunizations, exhibiting a clear dose response. Salivary IgA in immunized groups was significantly greater than that in the control group but displayed little dose-dependent kinetics, and, at the termination of the experiment, this response had not yet peaked. Lung lavage IgG and IgA were minimal after the primary immunization when the antibody was normalized to total protein but displayed dose-dependent kinetics after a secondary challenge. IgG peaked immediately after a secondary challenge, while IgA peak responses were observed only after 20 days. A positive correlation was noted between the serum, saliva, and lung lavage fluid IgGs after both primary and secondary immunizations and only after a secondary challenge for IgA. In this study we were able to elicit a secretory immune response, consisting of both IgG and IgA, which exhibited a dose-dependent characteristic in lung lavage fluid to this immunogen. Additionally, a positive correlation of antibody levels between saliva and lung lavage fluid suggests that saliva could be used as an indicator for monitoring specific antibody to M. pulmonis in lung lavage secretions without requiring invasive, deleterious procedures.
将甲醛固定的肺支原体与氢氧化铝作为佐剂一起,用于在大鼠唾液腺附近进行皮下免疫,以研究对该病原体的分泌性免疫反应特征。在血清以及外分泌液(即唾液和肺灌洗液)中检测到了针对这种微生物的特异性抗体诱导。在初次和二次局部免疫后,在这些液体中的每一种中都检测到了免疫球蛋白G(IgG)和IgA同种型抗体。免疫动物的血清反应明显大于对照组,但在所选择的免疫剂量下,无论是IgG还是IgA抗体均未观察到剂量反应。初次和二次免疫后,唾液IgG抗体反应均在早期达到峰值,呈现出明显的剂量反应。免疫组的唾液IgA明显高于对照组,但几乎没有剂量依赖性动力学,并且在实验结束时,这种反应尚未达到峰值。初次免疫后,当抗体以总蛋白进行标准化时,肺灌洗IgG和IgA含量极低,但在二次攻击后呈现出剂量依赖性动力学。二次攻击后IgG立即达到峰值,而IgA峰值反应仅在20天后观察到。初次和二次免疫后,血清、唾液和肺灌洗液IgG之间均存在正相关,而IgA仅在二次攻击后存在正相关。在本研究中,我们能够引发由IgG和IgA组成的分泌性免疫反应,该反应在肺灌洗液中对这种免疫原呈现出剂量依赖性特征。此外,唾液和肺灌洗液之间抗体水平的正相关表明,唾液可作为一种指标,用于监测肺灌洗分泌物中针对肺支原体的特异性抗体,而无需进行侵入性、有害的操作。