Stevens M G, Olsen S C, Pugh G W
Brucellosis Research Unit, U.S. Department of Agriculture, Agriculture Research Service, Ames, Iowa 50010, USA.
Infect Immun. 1995 Aug;63(8):3199-205. doi: 10.1128/iai.63.8.3199-3205.1995.
Mice vaccinated with Brucella abortus 19 (S19) or RB51 (SRB51) had spleen cells which proliferated in response to proteins of 32, 27, 18, and < 18 kDa but not in response to proteins of 106, 80, and 49 kDa from B. abortus 2308 (S2308) following vaccination and challenge infection with S2308. Spleen cells from mice vaccinated with S19 but not with SRB51 had increased proliferation in response to S2308 lipopolysaccharide (LPS) following challenge infection with S2308. We previously reported that mice vaccinated with S19 or SRB51, which were analyzed in the current study, have increased resistance to infection with S2308 and that only mice vaccinated with S19 produce antibody to S2308 LPS (M. Stevens, S. Olsen, G. Pugh, Jr., and D. Brees, Infect. Immun. 63:264-270, 1995). The results from our current and previous studies support the contention that vaccination of mice with S19 or SRB51 induces protection from infection with S2308 by cell-mediated immune responses to the same immunodominant (32, 27, 18, and < 18 kDa) protein antigens of S2308. In addition, the absence of S2308 LPS-responsive spleen cells and antibody to S2308 LPS in mice vaccinated with SRB51 suggests that immune responses to LPS have no role in SRB51-induced protective immunity.
用布鲁氏菌19(S19)或RB51(SRB51)疫苗接种的小鼠,其脾细胞在接种并经2308流产布鲁氏菌(S2308)攻击感染后,对分子量为32、27、18和<18 kDa的S2308蛋白有增殖反应,但对分子量为106、80和49 kDa的S2308蛋白无增殖反应。用S19而非SRB51疫苗接种的小鼠,在经S2308攻击感染后,其脾细胞对S2308脂多糖(LPS)的增殖反应增强。我们之前报道过,本研究中分析的用S19或SRB51疫苗接种的小鼠,对S2308感染的抵抗力增强,且只有用S19疫苗接种的小鼠产生针对S2308 LPS的抗体(M. Stevens、S. Olsen、G. Pugh, Jr.和D. Brees,《感染与免疫》63:264 - 270,1995)。我们当前和之前研究的结果支持这样的观点,即给小鼠接种S19或SRB51通过对S2308相同的免疫显性(32、27、18和<18 kDa)蛋白抗原的细胞介导免疫反应,诱导对S2308感染的保护作用。此外,用SRB51疫苗接种的小鼠缺乏对S2308 LPS有反应的脾细胞以及针对S2308 LPS的抗体,这表明对LPS的免疫反应在SRB51诱导的保护性免疫中不起作用。