Green S, Kurane I, Edelman R, Tacket C O, Eckels K H, Vaughn D W, Hoke C H, Ennis F A
Department of Medicine, University of Massachusetts Medical Center, Worcester 01655.
J Virol. 1993 Oct;67(10):5962-7. doi: 10.1128/JVI.67.10.5962-5967.1993.
We analyzed the CD4+ T-lymphocyte responses to dengue, West Nile, and yellow fever viruses 4 months after immunization of a volunteer with an experimental live-attenuated dengue virus type 1 vaccine (DEN-1 45AZ5). We examined bulk culture proliferation to noninfectious antigens, determined the precursor frequency of specific CD4+ T cells by limiting dilution, and established and analyzed CD4+ T-cell clones. Bulk culture proliferation was predominantly dengue virus type 1 specific with a lesser degree of cross-reactive responses to other dengue virus serotypes, West Nile virus, and yellow fever virus. Precursor frequency determination by limiting dilution in the presence of noninfectious dengue virus antigens revealed a frequency of antigen-reactive cells of 1 in 1,686 peripheral blood mononuclear cells (PBMC) for dengue virus type 1, 1 in 9,870 PBMC for dengue virus type 3, 1 in 14,053 PBMC for dengue virus type 2, and 1 in 17,690 PBMC for dengue virus type 4. Seventeen CD4+ T-cell clones were then established by using infectious dengue virus type 1 as antigen. Two patterns of dengue virus specificity were found in these clones. Thirteen clones were dengue virus type 1 specific, and four clones recognized both dengue virus types 1 and 3. Analysis of human leukocyte antigen (HLA) restriction revealed that five clones are HLA-DRw52 restricted, one clone is HLA-DP3 restricted, and one clone is HLA-DP4 restricted. These results indicate that in this individual, the CD4+ T-lymphocyte responses to immunization with live-attenuated dengue virus type 1 vaccine are predominantly serotype specific and suggest that a multivalent vaccine may be necessary to elicit strong serotype-cross-reactive CD4+ T-lymphocyte responses in such individuals.
我们在一名志愿者接种实验性1型减毒活登革病毒疫苗(DEN-1 45AZ5)4个月后,分析了其对登革病毒、西尼罗河病毒和黄热病毒的CD4+ T淋巴细胞反应。我们检测了对非感染性抗原的大量培养增殖情况,通过有限稀释法确定特异性CD4+ T细胞的前体频率,并建立和分析了CD4+ T细胞克隆。大量培养增殖主要是1型登革病毒特异性的,对其他登革病毒血清型、西尼罗河病毒和黄热病毒的交叉反应程度较低。在存在非感染性登革病毒抗原的情况下通过有限稀释法测定前体频率,结果显示1型登革病毒抗原反应性细胞在外周血单个核细胞(PBMC)中的频率为1/1686,3型登革病毒为1/9870 PBMC,2型登革病毒为1/14053 PBMC,4型登革病毒为1/17690 PBMC。然后以感染性1型登革病毒为抗原建立了17个CD4+ T细胞克隆。在这些克隆中发现了两种登革病毒特异性模式。13个克隆是1型登革病毒特异性的,4个克隆同时识别1型和3型登革病毒。对人类白细胞抗原(HLA)限制的分析表明,5个克隆受HLA-DRw52限制,1个克隆受HLA-DP3限制,1个克隆受HLA-DP4限制。这些结果表明,在该个体中,接种1型减毒活登革病毒疫苗后的CD4+ T淋巴细胞反应主要是血清型特异性的,并提示在此类个体中可能需要一种多价疫苗来引发强烈的血清型交叉反应性CD4+ T淋巴细胞反应。