Mongkolsapaya Juthathip, Dejnirattisai Wanwisa, Xu Xiao-ning, Vasanawathana Sirijitt, Tangthawornchaikul Nattaya, Chairunsri Aroonrung, Sawasdivorn Siraporn, Duangchinda Thaneeya, Dong Tao, Rowland-Jones Sarah, Yenchitsomanus Pa-thai, McMichael Andrew, Malasit Prida, Screaton Gavin
MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, OX3 9DS, UK.
Nat Med. 2003 Jul;9(7):921-7. doi: 10.1038/nm887.
Dengue virus presents a growing threat to public health in the developing world. Four major serotypes of dengue virus have been characterized, and epidemiological evidence shows that dengue hemorrhagic fever (DHF), the more serious manifestation of the disease, occurs more frequently upon reinfection with a second serotype. We have studied dengue virus-specific T-cell responses in Thai children. During acute infection, few dengue-responsive CD8+ T cells were recovered; most of those present showed an activated phenotype and were undergoing programmed cell death. Many dengue-specific T cells were of low affinity for the infecting virus and showed higher affinity for other, probably previously encountered strains. Profound T-cell activation and death may contribute to the systemic disturbances leading to DHF, and original antigenic sin in the T-cell responses may suppress or delay viral elimination, leading to higher viral loads and increased immunopathology.
登革病毒对发展中世界的公共卫生构成了日益严重的威胁。已鉴定出登革病毒的四种主要血清型,流行病学证据表明,登革热出血热(DHF)是该疾病更严重的表现形式,在再次感染第二种血清型时更频繁发生。我们研究了泰国儿童中针对登革病毒的T细胞反应。在急性感染期间,回收的登革病毒反应性CD8 + T细胞很少;其中大多数表现出活化表型并正在经历程序性细胞死亡。许多登革病毒特异性T细胞对感染病毒的亲和力较低,而对其他可能先前遇到的菌株具有更高的亲和力。深刻的T细胞活化和死亡可能导致导致DHF的全身紊乱,并且T细胞反应中的原始抗原罪可能抑制或延迟病毒清除,导致更高的病毒载量和增加的免疫病理学。