Institute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 4, 8093 Zürich, Switzerland.
Sir Alexander Fleming Building, South Kensington Campus, Imperial College London, London SW7 2AZ, UK.
Sci Immunol. 2017 Dec 1;2(18). doi: 10.1126/sciimmunol.aam8686.
During chronic viral infections, both CD8 and CD4 T cell responses are functionally compromised. Alongside exhaustion of CD8 T cells during chronic viral infections, it has also been documented that the CD4 T cells have an increased propensity to differentiate toward CXCR5 T follicular helper cell (T) lineage. Whether these T cells contribute to the immune response to chronic viral infection has remained unclear. Using chronic lymphocytic choriomeningitis virus (LCMV) infection in conjunction with an in vivo system where T cells can be conditionally ablated, we have established that these T cells do in fact play an important protective function. Specifically, we demonstrate that these T cells are essential for the late emergence of neutralizing LCMV-specific antibodies that keep viral titers in check and ultimately allow mice to clear the virus. By supporting the generation of neutralizing antibodies, we show that sustained activity of T cells promotes control of the chronic infection in face of exhausted CD8 T cell responses.
在慢性病毒感染期间,CD8 和 CD4 T 细胞反应均受到功能损害。在慢性病毒感染期间 CD8 T 细胞耗竭的同时,也有文献记录表明 CD4 T 细胞向 CXCR5 T 滤泡辅助细胞(Tfh)谱系分化的倾向增加。这些 T 细胞是否有助于慢性病毒感染的免疫反应尚不清楚。我们使用慢性淋巴细胞脉络丛脑膜炎病毒(LCMV)感染,并结合体内条件性细胞清除系统,证实这些 T 细胞确实发挥了重要的保护作用。具体而言,我们证明这些 T 细胞对于迟发性出现中和 LCMV 特异性抗体至关重要,这些抗体可以控制病毒滴度,并最终使小鼠清除病毒。通过支持中和抗体的产生,我们表明 T 细胞的持续活性促进了在耗尽的 CD8 T 细胞反应下对慢性感染的控制。