Byrne J A, Oldstone M B
J Virol. 1984 Sep;51(3):682-6. doi: 10.1128/JVI.51.3.682-686.1984.
Our data show that 1 X 10(7) to 1.5 X 10(7) lymphocytic choriomeningitis virus-specific, H-2-restricted cloned cytotoxic T lymphocytes (CTL) administered intravenously into acutely infected mice totally cleared virus from the spleens (10(4) to 10(5) PFU per spleen reduced to less than 50 PFU per spleen) by 24 h. This activity was genetically restricted in that cloned CTL could reduce titers of infectious virus in syngeneic C57BL/6 mice but not allogeneic BALB/c mice. Dose-response analysis indicated that at least 3 X 10(6) to 5 X 10(6) cloned CTL injected intravenously were needed to reduce significant amounts of infectious virus in the spleens. No infectious virus could be recovered from the spleens for at least 4 days after injection of cloned CTL. Hence, CTL play a major role in elimination of infectious virus from spleens during lymphocytic choriomeningitis virus infection. Our results also indicate that cloned CTL propagated in vitro for long periods of time can mediate a biologically relevant effect in vivo. These cells should be of considerable value in defining the precise manner in which CTL bring about control of viral infection, analyzing lymphocyte trafficking, and the potential use of cloned CTL in immunotherapy against viral disease.
我们的数据显示,将1×10⁷至1.5×10⁷个淋巴细胞性脉络丛脑膜炎病毒特异性、H-2限制性克隆细胞毒性T淋巴细胞(CTL)静脉注射到急性感染的小鼠体内,24小时内可使脾脏中的病毒完全清除(每个脾脏的病毒滴度从10⁴至10⁵ PFU降至每个脾脏低于50 PFU)。这种活性具有遗传限制性,即克隆的CTL可降低同基因C57BL/6小鼠而非异基因BALB/c小鼠中的传染性病毒滴度。剂量反应分析表明,静脉注射至少3×10⁶至5×10⁶个克隆的CTL才能显著降低脾脏中大量的传染性病毒。注射克隆的CTL后至少4天,脾脏中均未检测到传染性病毒。因此,CTL在淋巴细胞性脉络丛脑膜炎病毒感染期间从脾脏中清除传染性病毒的过程中发挥着主要作用。我们的结果还表明,在体外长时间培养的克隆CTL可在体内介导生物学相关效应。这些细胞在确定CTL控制病毒感染的精确方式、分析淋巴细胞运输以及克隆CTL在病毒性疾病免疫治疗中的潜在应用方面具有重要价值。