van Diemen P M, de Vries Reilingh G, Parmentier H K
Department of Animal Husbandry, Agricultural University, Wageningen, Netherlands.
Vet Immunol Immunopathol. 1994 Jun;41(3-4):307-21. doi: 10.1016/0165-2427(94)90104-x.
Experimental atrophic rhinitis (AR), serum antibody titres and in vitro lymphoproliferation to Pasteurella multocida derived toxin (Pm-T) were studied in piglets. Specific immune responses to Pm-T and Pm-T induced conchae atrophy were compared with AR immunity. This immunity was initiated by the Nobi-VAC AR-T vaccine administered at various times with respect to Pm-T challenge. Animals challenged with Pm-T developed conchae atrophy, but no antibodies nor cellular immune responses to Pm-T were detected. Vaccination 3 weeks before Pm-T challenge protected pigs against breakdown of nasal bony tissues. This protection was accompanied by an increase of serum antibodies and in vitro lymphoproliferation to Pm-T. Animals vaccinated 10 days before or after Pm-T challenge also had antibodies and cellular immune responses. However, these animals developed AR. In vitro, Pm-T appeared mitogenic for quiescent (non-immune) peripheral lymphocytes and Concanavalin A stimulated lymphocytes from some pigs. These in vitro lymphoproliferative responses could be partly abrogated by the addition of monomorphic anti-swine major histocompatibility complex class II DQ and DR specific monoclonal antibodies. We conclude that Pm-T is poorly immunogenic in vivo and does not initiate a protective Pm-T specific immune response. Pigs were protected from AR by vaccination, but protection was dependent on the timing of vaccine administration. We speculate that Pm-T modifies the immune response such that the response is not directed towards the toxin but to an unidentified component in the nose of piglets.
在仔猪中研究了实验性萎缩性鼻炎(AR)、血清抗体滴度以及对多杀性巴氏杆菌衍生毒素(Pm-T)的体外淋巴细胞增殖情况。将对Pm-T的特异性免疫反应和Pm-T诱导的鼻甲萎缩与AR免疫进行了比较。这种免疫是通过在不同时间相对于Pm-T攻击给予Nobi-VAC AR-T疫苗启动的。用Pm-T攻击的动物出现了鼻甲萎缩,但未检测到对Pm-T的抗体或细胞免疫反应。在Pm-T攻击前3周接种疫苗可保护猪的鼻骨组织不被破坏。这种保护伴随着血清抗体的增加以及对Pm-T的体外淋巴细胞增殖。在Pm-T攻击前或后10天接种疫苗的动物也有抗体和细胞免疫反应。然而,这些动物出现了AR。在体外,Pm-T对静止(非免疫)外周淋巴细胞以及来自一些猪的刀豆球蛋白A刺激的淋巴细胞具有促有丝分裂作用。添加单克隆抗猪主要组织相容性复合体II类DQ和DR特异性单克隆抗体可部分消除这些体外淋巴细胞增殖反应。我们得出结论,Pm-T在体内免疫原性较差,不会引发保护性的Pm-T特异性免疫反应。通过接种疫苗可保护猪不患AR,但保护作用取决于疫苗接种的时间。我们推测,Pm-T改变了免疫反应,使得该反应不是针对毒素,而是针对仔猪鼻腔中一种未确定的成分。