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Elicitation of Simian Immunodeficiency Virus-Specific Cytotoxic T Lymphocytes in Mucosal Compartments of Rhesus Monkeys by Systemic Vaccination

机译:通过全身免疫接种在猕猴粘膜腔中诱导猿猴免疫缺陷病毒特异的细胞毒性T淋巴细胞

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摘要

Since most human immunodeficiency virus (HIV) infections are initiated following mucosal exposure to the virus, the anatomic containment or abortion of an HIV infection is likely to require vaccine-elicited cellular immune responses in those mucosal sites. Studying vaccine-elicited mucosal immune responses has been problematic because of the difficulties associated with sampling T lymphocytes from those anatomic compartments. In the present study, we demonstrate that mucosal cytotoxic T lymphocytes (CTL) specific for simian immunodeficiency virus (SIV) and simian HIV can be reproducibly sampled from intestinal mucosal tissue of rhesus monkeys obtained under endoscopic guidance. These lymphocytes recognize peptide-major histocompatibility complex class I complexes and express gamma interferon on exposure to peptide antigen. Interestingly, systemic immunization of monkeys with plasmid DNA immunogens followed by live recombinant attenuated poxviruses or adenoviruses with genes deleted elicits high-frequency SIV-specific CTL responses in these mucosal tissues. These studies therefore suggest that systemic delivery of potent HIV immunogens may suffice to elicit substantial mucosal CTL responses.
机译:由于大多数人类免疫缺陷病毒(HIV)感染是在粘膜暴露于该病毒后引发的,因此,HIV感染的解剖抑制或流产可能需要在这些粘膜部位进行疫苗诱导的细胞免疫反应。研究疫苗引起的粘膜免疫反应一直是有问题的,因为与从那些解剖区室采集T淋巴细胞有关的困难。在本研究中,我们证明可以从内窥镜指导下获得的恒河猴肠粘膜组织中可复制地采样特异于猿猴免疫缺陷病毒(SIV)和猿猴HIV的粘膜细胞毒性T淋巴细胞(CTL)。这些淋巴细胞识别肽-主要组织相容性复合物I类复合物,并在暴露于肽抗原时表达γ干扰素。有趣的是,先用质粒DNA免疫原对猴子进行全身免疫,再用活的重组减毒痘病毒或缺失基因的腺病毒对猴子进行全身免疫,在这些粘膜组织中引起高频SIV特异性CTL反应。因此,这些研究表明,系统性递送有效的HIV免疫原可能足以引起实质性的粘膜CTL反应。

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