Mastroeni P, Villarreal-Ramos B, Hormaeche C E
Department of Pathology, University of Cambridge, U.K.
Microb Pathog. 1992 Dec;13(6):477-91. doi: 10.1016/0882-4010(92)90014-f.
The SL3261 Salmonella typhimurium aroA live vaccine strain confers solid protection against oral challenge with virulent salmonellae, immunity persisting long after the vaccine has been cleared from the tissues. BALB/c mice immunized with SL3261 and later subjected to in vivo depletion of both CD4+ and CD8+ T cells had impaired recall of immunity to oral challenge with the virulent S. typhimurium C5, with increased mortality and higher bacterial loads in the reticuloendothelial system (RES). Selective depletion of CD4+ cells alone significantly impaired resistance both 8 and 14 weeks after vaccination as determined by estimation of bacterial numbers in organ homogenates. Depletion of CD8+ cells alone had less effect on immunity when performed at 8 weeks than at 14 weeks after immunization. Administration of anti-IFN gamma or anti-TNF alpha antibodies also impaired recall of immunity, exacerbating a secondary infection in vaccinated mice. Challenge of T cell-depleted immune mice with virulent salmonellae caused hepatosplenomegaly with minute grossly visible focal lesions, and a marked increase in the number and severity of necrotic foci in spleen, liver and lymph nodes. A widespread mononuclear cell infiltrate was present. The histopathology in anti-IFN gamma-treated mice was qualitatively similar to that seen in T-cell depleted mice. In contrast, in the anti-TNF alpha-treated mice splenomegaly was much less than in T cell-depleted mice. Granulomas were absent, no mononuclear infiltration was observed and there was severe necrosis; the lesions appeared similar to or worse than those seen in naïve mice. Surprisingly, IFN gamma was detectable in sera of both controls and T cell-depleted mice on day 8 of the secondary infection, as well as in sera of anti-TNF alpha-treated mice on day 6 of infection. The results indicate that T cells, IFN gamma and TNF alpha are all important in the specific recall of immunity to virulent salmonellae conferred by immunization with live vaccines, with the effect of T cell and IFN gamma depletion (marked macrophage infiltration) being qualitatively very different from that of TNF alpha neutralization (no mononuclear infiltrate or granuloma formation).
SL3261鼠伤寒沙门氏菌aroA活疫苗株能有效抵御强毒性沙门氏菌的口服攻击,即使在疫苗已从组织中清除很久之后,免疫力依然存在。用SL3261免疫的BALB/c小鼠,随后体内CD4+和CD8+ T细胞均被清除,其对强毒性鼠伤寒沙门氏菌C5口服攻击的免疫回忆受损,死亡率增加,网状内皮系统(RES)中的细菌载量更高。仅选择性清除CD4+细胞,在接种疫苗8周和14周后,通过估计器官匀浆中的细菌数量确定,显著损害了抵抗力。仅在免疫后8周清除CD8+细胞对免疫力的影响小于14周时。给予抗IFNγ或抗TNFα抗体也会损害免疫回忆,加重接种疫苗小鼠的继发感染。用强毒性沙门氏菌攻击T细胞耗竭的免疫小鼠会导致肝脾肿大,有微小的肉眼可见局灶性病变,脾脏、肝脏和淋巴结中的坏死灶数量和严重程度显著增加。存在广泛的单核细胞浸润。抗IFNγ处理小鼠的组织病理学与T细胞耗竭小鼠的定性相似。相比之下,抗TNFα处理小鼠的脾肿大比T细胞耗竭小鼠小得多。没有肉芽肿,未观察到单核细胞浸润,且有严重坏死;病变似乎与未免疫小鼠所见相似或更严重。令人惊讶的是,在继发感染第8天,对照组和T细胞耗竭小鼠的血清中均可检测到IFNγ,在感染第6天,抗TNFα处理小鼠的血清中也可检测到。结果表明,T细胞、IFNγ和TNFα在活疫苗免疫赋予的对强毒性沙门氏菌免疫的特异性回忆中都很重要,T细胞和IFNγ耗竭的影响(明显的巨噬细胞浸润)与TNFα中和的影响(无单核细胞浸润或肉芽肿形成)在性质上非常不同。