Pockley A G, Montgomery P C
Department of Immunology and Microbiology, Wayne State University School of Medicine, Detroit, Michigan 48201.
Immunology. 1991 May;73(1):19-23.
Interleukins 5 and 6 have previously been shown to exhibit IgA-enhancing activity in vitro. This study investigated the effect of IL-5 and IL-6 on antigen-specific tear IgA antibody responses in vivo. Rats were given primary and secondary immunizations by the ocular-topical (OT) route with either antigen (DNP-Pn) alone or antigen plus IL-5 and IL-6 (IL-5/6). Antigen was administered for the first 3 days of each stimulation cycle and lymphokines (50 units of each lymphokine/eye/day) or control media for the first 7 days of the primary and secondary immunizations. Co-administration of antigen with IL-5/6 markedly enhanced (approximately three-fold) the secondary tear IgA anti-DNP antibody response in the lymphokine-treated group. Enhanced tear IgA antibody responses were maintained in the lymphokine-treated group following a tertiary immunization in the absence of IL-5/6. There was no apparent effect on the total tear IgA levels in either group of animals. Ocular topical immunization also elicited secondary and tertiary serum IgG antibody responses which were not affected by the administration of IL-5/6. Neither secondary nor tertiary serum IgM antibody responses were detected in either group of animals. These data indicate that IL-5 and IL-6 are able to augment tear IgA antibody responses in vivo. That the enhancement was maintained following a subsequent antigenic challenge in the absence of the lymphokines suggests a potential therapeutic application for lymphokines in augmenting IgA responses at mucosal surfaces.
白细胞介素5和6此前已被证明在体外具有增强IgA的活性。本研究调查了白细胞介素5和6对体内抗原特异性泪液IgA抗体反应的影响。通过眼局部(OT)途径,用单独的抗原(二硝基苯 - 肺炎球菌多糖,DNP-Pn)或抗原加白细胞介素5和6(IL-5/6)对大鼠进行初次和二次免疫。在每个刺激周期的前3天给予抗原,在初次和二次免疫的前7天给予淋巴因子(每种淋巴因子50单位/眼/天)或对照培养基。抗原与IL-5/6共同给药显著增强了(约三倍)淋巴因子处理组中二次泪液IgA抗DNP抗体反应。在没有IL-5/6的情况下进行三次免疫后,淋巴因子处理组中泪液IgA抗体反应增强得以维持。两组动物的总泪液IgA水平均未受到明显影响。眼局部免疫还引发了二次和三次血清IgG抗体反应,这些反应不受IL-5/6给药的影响。两组动物均未检测到二次或三次血清IgM抗体反应。这些数据表明,IL-5和IL-6能够在体内增强泪液IgA抗体反应。在没有淋巴因子的情况下,后续抗原攻击后增强作用仍得以维持,这表明淋巴因子在增强粘膜表面IgA反应方面具有潜在的治疗应用价值。