Appanna Ramapraba, Huat Tan Lian, See Lucy Lum Chai, Tan Phoay Lay, Vadivelu Jamuna, Devi Shamala
Department of Medical Microbiology, Faculty of Medicine, University Malaya, 50603, Kuala Lumpur, Malaysia.
Clin Vaccine Immunol. 2007 Aug;14(8):969-77. doi: 10.1128/CVI.00069-07. Epub 2007 Jun 13.
Dengue virus infections are a major cause of morbidity and mortality in tropical and subtropical areas in the world. Attempts to develop effective vaccines have been hampered by the lack of understanding of the pathogenesis of the disease and the absence of suitable experimental models for dengue viral infection. The magnitude of T-cell responses has been reported to correlate with dengue disease severity. Sixty Malaysian adults with dengue viral infections were investigated for their dengue virus-specific T-cell responses to 32 peptides antigens from the structural and nonstructural regions from a dengue virus isolate. Seventeen different peptides from the C, E, NS2B, NS3, NS4A, NS4B, and NS5 regions were found to evoke significant responses in a gamma interferon enzyme-linked immunospot (ELISPOT) assay of samples from 13 selected patients with dengue fever (DF) and dengue hemorrhagic fever (DHF). NS3 and predominantly NS3(422-431) were found to be important T-cell targets. The highest peaks of T-cell responses observed were in responses to NS3(422-431) and NS5(563-571) in DHF patients. We also found almost a sevenfold increase in T-cell response in three DHF patients compared to three DF patient responses to peptide NS3(422-431). A large number of patients' T cells also responded to the NS2B(97-106) region. The ELISPOT analyses also revealed high frequencies of T cells that recognize both serotype-specific and cross-reactive dengue virus antigens in patients with DHF.
登革病毒感染是世界热带和亚热带地区发病和死亡的主要原因。由于对该疾病发病机制缺乏了解以及缺乏适合登革病毒感染的实验模型,开发有效疫苗的尝试受到了阻碍。据报道,T细胞反应的强度与登革热疾病严重程度相关。对60名感染登革病毒的马来西亚成年人进行了研究,检测他们对来自一种登革病毒分离株结构和非结构区域的32种肽抗原的登革病毒特异性T细胞反应。在对13名选定的登革热(DF)和登革出血热(DHF)患者的样本进行的γ干扰素酶联免疫斑点(ELISPOT)分析中,发现来自C、E、NS2B、NS3、NS4A、NS4B和NS5区域的17种不同肽能引发显著反应。发现NS3以及主要是NS3(422 - 431)是重要的T细胞靶点。在DHF患者中观察到的T细胞反应最高峰是对NS3(422 - 431)和NS5(563 - 571)的反应。我们还发现,与三名DF患者对肽NS3(422 - 431)的反应相比,三名DHF患者的T细胞反应几乎增加了七倍。大量患者的T细胞也对NS2B(97 - 106)区域有反应。ELISPOT分析还显示,DHF患者中识别血清型特异性和交叉反应性登革病毒抗原的T细胞频率很高。