Park Y H, Fox L K, Hamilton M J, Davis W C
Dept. of Veterinary Microbiology and Pathology, Washington State University, Pullman 99164.
Vet Immunol Immunopathol. 1993 Mar;36(2):137-51. doi: 10.1016/0165-2427(93)90103-b.
Investigations were conducted to determine the mechanisms that account for differences in the responses of BoCD4+ lymphocytes from mammary gland secretions (MGS) in healthy cows and in cows with Staphylococcus aureus infection. The proliferative response to lectins and S. aureus antigens of mammary gland lymphocytes from healthy, S. aureus immunized cows was less than the response of peripheral blood lymphocytes. The lower responses of mammary gland lymphocytes were attributable both to less efficient antigen presentation by mammary gland antigen-presenting cells (APC) than by peripheral blood APC, and to lower responsiveness of mammary gland lymphocytes to lectins and antigen. In addition, the proliferative response of infected mammary gland lymphocytes was less than the response of uninfected mammary gland lymphocytes. This difference resulted from decreased proliferation of BoCD4+ lymphocytes in infected MGS. Flow cytometric analysis revealed that infected MGS contained increased numbers of BoCD8+ cells which coexpressed an activation molecule, ACT2, relative to BoCD8+ cells from uninfected MGS. Removal of BoCD8+, ACT2+ lymphocytes resulted in increased antigen responsiveness by lymphocytes from infected mammary glands. Also, when purified BoCD4+ lymphocytes were stimulated with antigen in the presence of varying numbers of ACT2+, BoCD8+ lymphocytes, antigen responsiveness was decreased in a dose-related manner. These data demonstrate that hyporesponsiveness of mammary gland lymphocytes to lectins and S. aureus antigen is, in part, mediated by activated BoCD8+ lymphocytes and suggest that this population enhances persistent intramammary infection by S. aureus.
开展了多项研究,以确定健康奶牛和感染金黄色葡萄球菌的奶牛乳腺分泌物(MGS)中BoCD4 +淋巴细胞反应存在差异的机制。健康的、经金黄色葡萄球菌免疫的奶牛乳腺淋巴细胞对凝集素和金黄色葡萄球菌抗原的增殖反应低于外周血淋巴细胞的反应。乳腺淋巴细胞反应较低的原因,一方面是乳腺抗原呈递细胞(APC)的抗原呈递效率低于外周血APC,另一方面是乳腺淋巴细胞对凝集素和抗原的反应性较低。此外,感染的乳腺淋巴细胞的增殖反应低于未感染的乳腺淋巴细胞。这种差异是由于感染的MGS中BoCD4 +淋巴细胞增殖减少所致。流式细胞术分析显示,相对于未感染MGS的BoCD8 +细胞,感染的MGS中共同表达激活分子ACT2的BoCD8 +细胞数量增加。去除BoCD8 +、ACT2 +淋巴细胞可导致感染乳腺的淋巴细胞对抗原的反应性增加。此外,当用抗原刺激纯化的BoCD4 +淋巴细胞时,在存在不同数量的ACT2 +、BoCD8 +淋巴细胞的情况下,抗原反应性呈剂量依赖性降低。这些数据表明,乳腺淋巴细胞对凝集素和金黄色葡萄球菌抗原的低反应性部分是由活化的BoCD8 +淋巴细胞介导的,并表明这群细胞增强了金黄色葡萄球菌引起的乳腺持续性感染。