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异源 DENV 特异性 CD8T 淋巴细胞在二次登革病毒感染免疫功能正常小鼠模型中的作用。

The Role of Heterotypic DENV-specific CD8T Lymphocytes in an Immunocompetent Mouse Model of Secondary Dengue Virus Infection.

机构信息

Fundación INFANT, Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina.

Fundación INFANT, Buenos Aires, Argentina.

出版信息

EBioMedicine. 2017 Jun;20:202-216. doi: 10.1016/j.ebiom.2017.04.033. Epub 2017 Apr 27.

Abstract

Dengue is the most prevalent arthropod-borne viral disease worldwide and is caused by the four dengue virus serotypes (DENV-1-4). Sequential heterologous DENV infections can be associated with severe disease manifestations. Here, we present an immunocompetent mouse model of secondary DENV infection using non mouse-adapted DENV strains to investigate the pathogenesis of severe dengue disease. C57BL/6 mice infected sequentially with DENV-1 (strain Puerto Rico/94) and DENV-2 (strain Tonga/74) developed low platelet counts, internal hemorrhages, and increase of liver enzymes. Cross-reactive CD8 T lymphocytes were found to be necessary and sufficient for signs of severe disease by adoptively transferring of DENV-1-immune CD8T lymphocytes before DENV-2 challenge. Disease signs were associated with production of tumor necrosis factor (TNF)-α and elevated cytotoxicity displayed by heterotypic anti-DENV-1 CD8 T lymphocytes. These findings highlight the critical role of heterotypic anti-DENV CD8 T lymphocytes in manifestations of severe dengue disease.

摘要

登革热是全球最普遍的虫媒病毒病,由四种登革病毒血清型(DENV-1-4)引起。继发的异型登革病毒感染可能与严重疾病表现有关。在这里,我们使用非适应于小鼠的登革病毒株建立了继发感染的免疫功能正常的小鼠模型,以研究严重登革热疾病的发病机制。用 DENV-1(波多黎各/94 株)和 DENV-2(汤加/74 株)先后感染 C57BL/6 小鼠可导致血小板计数降低、内出血和肝酶升高。通过在 DENV-2 攻击前过继转移 DENV-1 免疫 CD8 T 淋巴细胞,发现交叉反应性 CD8 T 淋巴细胞是发生严重疾病的必要和充分条件。疾病征象与肿瘤坏死因子(TNF)-α的产生以及异型抗 DENV-1 CD8 T 淋巴细胞显示的细胞毒性升高有关。这些发现强调了异型抗 DENV CD8 T 淋巴细胞在严重登革热疾病表现中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09bd/5478214/f26f35eee752/gr1.jpg

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