Zucker-Franklin D, Fraig M, Grusky G
Department of Medicine, New York University Medical Center, New York 10016, USA.
Clin Diagn Lab Immunol. 1995 May;2(3):343-8. doi: 10.1128/cdli.2.3.343-348.1995.
Although it is known that impairment of dendritic cells (DC) plays a role in the pathogenesis and immunosuppression of retrovirus-associated diseases, it is not clear whether, or to what extent, these antigen-presenting cells themselves become infected. The realization that the cells can be generated in vitro in larger numbers than can be isolated from circulating blood or bone marrow raised the possibility that they could be used for therapeutic purposes. Therefore, we investigated whether DC generated in vitro from CD34 precursors are susceptible to infection when cocultured with human immunodeficiency virus type 1- or human T-cell leukemia/lymphoma virus-infected cell lines. While there appears to be a remarkable affinity of the viruses for the plasma membranes of the DC, interiorization or budding was not observed in 30 experiments carried out under a variety of conditions.
尽管已知树突状细胞(DC)功能受损在逆转录病毒相关疾病的发病机制和免疫抑制中起作用,但尚不清楚这些抗原呈递细胞本身是否被感染以及感染程度如何。人们认识到,这些细胞在体外生成的数量比从循环血液或骨髓中分离出的数量更多,这增加了它们可用于治疗目的的可能性。因此,我们研究了从CD34前体细胞体外生成的DC与1型人类免疫缺陷病毒或人类T细胞白血病/淋巴瘤病毒感染的细胞系共培养时是否易受感染。虽然这些病毒似乎对DC的质膜有显著亲和力,但在各种条件下进行的30次实验中均未观察到内化或出芽现象。