Stevenson P G, Belz G T, Altman J D, Doherty P C
Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Eur J Immunol. 1999 Apr;29(4):1059-67. doi: 10.1002/(SICI)1521-4141(199904)29:04<1059::AID-IMMU1059>3.0.CO;2-L.
The murine gamma-herpesvirus MHV-68 causes an acute, transient pneumonitis, followed by an infectious mononucleosis (IM)-like illness with splenomegaly, widespread latent infection of B lymphocytes and an expansion of Vbeta4+ CD8+ T cells. CD8+ T cells specific for an H-2Db-restricted epitope were prominent during the acute respiratory infection, but their prevalence declined rapidly during the mononucleosis. In contrast, CD8+ T cells specific for an H-2Kb-restricted epitope, apparently expressed by virus-infected B lymphocytes, were most numerous during the mononucleosis illness and were maintained at relatively high frequencies thereafter. The prevalence of all peptide-specific CD8+ T cells decreased during the expansion of the Vbeta4+ CD8+ population, which did not recognize any peptide epitopes identified and was apparent also in an MHC class I-deficient environment. The CD8+ T cell population recognizing productively infected epithelial cells thus differed substantially from that responding during the IM illness.
鼠γ-疱疹病毒MHV-68可引起急性、短暂性肺炎,随后出现类似传染性单核细胞增多症(IM)的疾病,伴有脾肿大、B淋巴细胞广泛潜伏感染以及Vβ4 + CD8 + T细胞扩增。在急性呼吸道感染期间,对H-2Db限制性表位具有特异性的CD8 + T细胞很突出,但在单核细胞增多症期间其患病率迅速下降。相比之下,对H-2Kb限制性表位具有特异性的CD8 + T细胞,显然由病毒感染的B淋巴细胞表达,在单核细胞增多症疾病期间数量最多,此后维持在相对较高的频率。在Vβ4 + CD8 +群体扩增期间,所有肽特异性CD8 + T细胞的患病率均下降,该群体不识别任何已鉴定的肽表位,在MHC I类缺陷环境中也很明显。因此,识别有效感染上皮细胞的CD8 + T细胞群体与IM疾病期间反应的群体有很大不同。