Department of Veterinary Molecular Biology, Montana State University, Bozeman, Montana 59717, USA.
Infect Immun. 2010 Jul;78(7):3019-26. doi: 10.1128/IAI.00101-10. Epub 2010 Mar 29.
The mechanisms of the primary adaptive immune response to Coxiella burnetii are not well known. Following inoculation of the lungs with C. burnetii Nine Mile phase I (NMI), SCID mice developed pneumonia and splenomegaly and succumbed to infection, whereas wild-type mice cleared the infection by 24 days. SCID mice reconstituted with either CD4+ T cells or CD8+ T cells alone were able to control the infection, indicating that the presence of either type of T cells was sufficient to control infection, and B cells were not necessary for primary immunity. Similarly, wild-type mice depleted of either CD4+ T cells or CD8+ T cells controlled infections in their lungs, but these mice were highly susceptible if they were depleted of both types of T cells. However, compared to CD4+ T-cell-dependent protection, CD8+ T-cell-dependent protection resulted in less inflammation in the lungs and less growth of bacteria in the spleens.
对科氏考克斯体初次适应性免疫应答的机制尚不清楚。在通过肺部接种科氏考克斯体九英里一期(NMI)后,SCID 小鼠发生肺炎和脾肿大,并感染致死,而野生型小鼠在 24 天内清除了感染。单独用 CD4+T 细胞或 CD8+T 细胞重建的 SCID 小鼠能够控制感染,表明存在任何一种类型的 T 细胞都足以控制感染,B 细胞对于初次免疫不是必需的。同样,野生型小鼠耗尽 CD4+T 细胞或 CD8+T 细胞也能控制肺部感染,但如果两种 T 细胞都被耗尽,这些小鼠就极易感染。然而,与 CD4+T 细胞依赖性保护相比,CD8+T 细胞依赖性保护导致肺部炎症减少,脾脏中细菌生长减少。