Gasbarre L C, Suter P, Fayer R
Am J Vet Res. 1984 Aug;45(8):1592-6.
Cattle inoculated with Sarcocystis bovicanis (= Sarcocystis cruzi) and sheep inoculated with Sarcocystis ovicanis were monitored for the appearance of Sarcocystis-specific antibodies and lymphocytes in the peripheral circulation. Anti-Sarcocystis antibody was identified by enzyme-linked immunosorbent assay, whereas antigen-reactive lymphocytes were discerned by an in vitro lymphocyte blastogenic assay. The antigens used were the soluble fraction recovered from disrupted bradyzoites of mature sarcocysts. Cattle developed anti-Sarcocystis immunoglobulin (Ig)M responses, beginning 3 to 4 weeks after inoculation, and IgG1 antibody responses, beginning 5 to 6 weeks after inoculation. The increase in IgM antibody was relatively brief, returning to near preinfection levels in 2 to 3 months. In contrast, IgG1 antibody levels remained high for at least 5 to 6 months. Neither IgG2 nor IgA antibody responses were demonstrable in cattle. In sheep, the IgG antibody levels followed a time course similar to that seen in cattle, except that the increase was slightly delayed (6 to 8 weeks after inoculation was done). Measurable IgM antibody response was not seen in sheep. Cellular immunoresponsiveness as judged by in vitro lymphocyte blastogenesis in cattle was different from that in sheep. Sarcocystis-specific lymphocytes were demonstrable in the circulation of cattle within 15 days after they were inoculated, but the activity decreased rapidly. In sheep, reactive cells were not evident until 3 to 4 weeks after inoculation were done, but peripheral blood lymphocytes taken from these sheep as long as 5 to 6 weeks after the inoculations remained capable of mounting strong blastogenic responses. Neither the enzyme-linked immunosorbent assay nor the blastogenic assay showed species specificity. Animals immunized with a given species of Sarcocystis gave similar in vitro responses to antigens from the immunizing species and to other species of Sarcocystis.(ABSTRACT TRUNCATED AT 250 WORDS)
对接种牛犬肉孢子虫(= 克鲁斯肉孢子虫)的牛和接种绵羊肉孢子虫的绵羊进行监测,观察外周循环中肉孢子虫特异性抗体和淋巴细胞的出现情况。通过酶联免疫吸附测定法鉴定抗肉孢子虫抗体,而通过体外淋巴细胞增殖测定法识别抗原反应性淋巴细胞。所用抗原是从成熟包囊的缓殖子破碎物中回收的可溶性部分。牛在接种后3至4周开始产生抗肉孢子虫免疫球蛋白(Ig)M反应,在接种后5至6周开始产生IgG1抗体反应。IgM抗体的增加相对短暂,在2至3个月内恢复到接近感染前水平。相比之下,IgG1抗体水平至少在5至6个月内保持较高。在牛中未检测到IgG2和IgA抗体反应。在绵羊中,IgG抗体水平的变化时间进程与牛相似,只是增加稍有延迟(接种后6至8周)。在绵羊中未观察到可测量的IgM抗体反应。通过体外淋巴细胞增殖判断的细胞免疫反应性在牛和绵羊中有所不同。接种后15天内,牛的循环中可检测到肉孢子虫特异性淋巴细胞,但其活性迅速下降。在绵羊中,直到接种后3至4周才有反应性细胞出现,但在接种后长达5至6周从这些绵羊采集的外周血淋巴细胞仍能够产生强烈的增殖反应。酶联免疫吸附测定法和增殖测定法均未显示种属特异性。用给定种类的肉孢子虫免疫的动物对来自免疫种类的抗原和其他种类的肉孢子虫抗原产生相似的体外反应。(摘要截短于250字)