Fenwick B W, Osburn B I
Infect Immun. 1986 Nov;54(2):575-82. doi: 10.1128/iai.54.2.575-582.1986.
The immunologic responses to a smooth-type lipopolysaccharide (LPS) (HpS-LPS), a rough-type LPS (HpR-LPS), and a capsular-enriched polysaccharide preparation (HpC-PS) purified from Haemophilus pleuropneumoniae were determined in pigs immunized with a commercial H. pleuropneumoniae cellular vaccine, in pigs experimentally infected with H. pleuropneumoniae, in control pigs, and in immunized rabbits. The ability of the preparations to induce lymphocyte blastogenesis and B-cell activation was determined in the pigs and compared with the responses induced by the LPS of Escherichia coli O111:B4 and the LPS of Salmonella minnesota Re595. All the LPS preparations acted to induce proliferation of peripheral blood lymphocytes (PBL) from all pigs. The blastogenic response of PBL from H. pleuropneumoniae-infected pigs to HpS-LPS and HpR-LPS was significantly (P less than 0.05) greater than that of PBL from immunized and control pigs. HpC-PS did not induce a blastogenic response in the PBL of control pigs but did in PBL from H. pleuropneumoniae-infected pigs and to a greater degree in immunized pigs. An increase in the response of PBL to the S. minnesota LPS occurred only in the H. pleuropneumoniae-infected pigs. Significantly more (P less than 0.05) immunoglobulin-secreting cells (ISC) were induced in a reverse hemolytic plaque assay by stimulation with HpS-LPS and HpC-PS of PBL isolated from pigs infected with H. pleuropneumoniae than of PBL from immunized pigs. Increasing the number of T cells increased the number of ISC induced by HpS-LPS in control and immunized pigs, but not in convalescent pigs. The presence of macrophages reduced activation of ISC by HpS-LPS in control pigs and to a lesser degree in immunized pigs, whereas in H. pleuropneumoniae-infected pigs macrophages enhanced the induction of ISC by HpS-LPS. In immunized pigs, macrophages acted to inhibit the ability of HpC-PS to induce ISC. Serologic studies indicate that HpC-PS contains strain- and serotype-specific antigens; that HpS-LPS has both serotype-specific and cross-reacting species-specific antigens; and that HpR-LPS does not contain detectable serotype-specific antigens but does have both non species- and species-specific antigens. These studies show that the serotype-specific protection provided by immunization of pigs with an H. pleuropneumoniae cellular vaccine is principally the result of immunity to capsular antigens and that a weak cellular immune response occurs as compared with that induced by infection with H. pleuropneumoniae.(ABSTRACT TRUNCATED AT 400 WORDS)
在接种了猪肺炎支原体细胞疫苗的猪、实验感染猪肺炎支原体的猪、对照猪以及免疫兔中,测定了对从猪肺炎支原体中纯化出的光滑型脂多糖(LPS)(HpS-LPS)、粗糙型LPS(HpR-LPS)和富含荚膜的多糖制剂(HpC-PS)的免疫反应。在猪中测定了这些制剂诱导淋巴细胞增殖和B细胞活化的能力,并与大肠杆菌O111:B4的LPS和明尼苏达沙门氏菌Re595的LPS诱导的反应进行比较。所有LPS制剂均能诱导所有猪外周血淋巴细胞(PBL)增殖。猪肺炎支原体感染猪的PBL对HpS-LPS和HpR-LPS的增殖反应显著(P小于0.05)高于免疫猪和对照猪的PBL。HpC-PS在对照猪的PBL中未诱导增殖反应,但在猪肺炎支原体感染猪的PBL中能诱导,且在免疫猪中诱导程度更高。仅在猪肺炎支原体感染猪中,PBL对明尼苏达沙门氏菌LPS的反应有所增加。在反向溶血空斑试验中,用HpS-LPS和HpC-PS刺激从猪肺炎支原体感染猪分离的PBL,比刺激免疫猪的PBL诱导出显著更多(P小于0.05)的免疫球蛋白分泌细胞(ISC)。增加T细胞数量可增加对照猪和免疫猪中HpS-LPS诱导的ISC数量,但在恢复期猪中无此作用。巨噬细胞的存在降低了对照猪中HpS-LPS对ISC的活化作用,在免疫猪中作用较小,而在猪肺炎支原体感染猪中,巨噬细胞增强了HpS-LPS对ISC的诱导作用。在免疫猪中,巨噬细胞抑制了HpC-PS诱导ISC的能力。血清学研究表明,HpC-PS含有菌株和血清型特异性抗原;HpS-LPS既有血清型特异性抗原,也有交叉反应的种特异性抗原;HpR-LPS不含有可检测到的血清型特异性抗原,但有非种特异性和种特异性抗原。这些研究表明,用猪肺炎支原体细胞疫苗免疫猪所提供的血清型特异性保护主要是对荚膜抗原免疫的结果,与猪肺炎支原体感染诱导的细胞免疫反应相比,细胞免疫反应较弱。(摘要截短至400字)