PloS one · 2013
Detection of JC virus-specific immune responses in a novel humanized mouse model.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Tan Chen Sabrina, Broge Thomas A, Seung Edward, Vrbanac Vlad, Viscidi Raphael, Gordon Jennifer, Tager Andrew M, Koralnik Igor J
Аннотация
Progressive Multifocal Leukoencephalopathy (PML) is an often fatal disease caused by the reactivation of the JC virus (JCV). Better understanding of viral-host interactions has been hampered by the lack of an animal model. Engrafting NOD/SCID/IL-2-Rg (null) mice with human lymphocytes and thymus, we generated a novel animal model for JCV infection. Mice were inoculated with either a PML isolate, JCV Mad-4, or with JCV CY, found in the kidney and urine of healthy individuals. While mice remained asymptomatic following inoculation, JCV DNA was occasionally detected in both the blood and the urine compartments. Mice generated both humoral and cellular immune responses against JCV. Expressions of immune exhaustion marker, PD-1, on lymphocytes were consistent with response to infection. Using this model we present the first in vivo demonstration of virological and immunological differences between JCV Mad-4 and CY. This model may prove valuable for studying JCV host immune responses.
Предметные рубрики MeSH
AnimalsAntibodies, ViralAntigens, DifferentiationAntigens, ViralCOS CellsCapsid ProteinsChlorocebus aethiopsDNA, ViralDisease Models, AnimalHumansImmunity, CellularImmunity, HumoralJC VirusKidneyLeukoencephalopathy, Progressive MultifocalMiceMice, Inbred NODMice, SCIDProgrammed Cell Death 1 Receptor