Williams K C, Corey S, Westmoreland S V, Pauley D, Knight H, deBakker C, Alvarez X, Lackner A A
Division of Comparative Pathology, New England Regional Primate Research Center, Harvard Medical School, Southborough, Massachusetts 01772, USA.
J Exp Med. 2001 Apr 16;193(8):905-15. doi: 10.1084/jem.193.8.905.
The macrophage is well established as a target of HIV and simian immunodeficiency virus (SIV) infection and a major contributor to the neuropathogenesis of AIDS. However, the identification of distinct subpopulations of monocyte/macrophages that carry virus to the brain and that sustain infection within the central nervous system (CNS) has not been examined. We demonstrate that the perivascular macrophage and not the parenchymal microglia is the primary cell productively infected by SIV. We further demonstrate that although productive viral infection of the CNS occurs early, thereafter it is not easily detectable until terminal AIDS. The biology of perivascular macrophages, including their rate of turnover and replacement by peripheral blood monocytes, may explain the timing of neuroinvasion, disappearance, and reappearance of virus in the CNS, and questions the ability of the brain to function as a reservoir for productive infection by HIV/SIV.
巨噬细胞作为HIV和猴免疫缺陷病毒(SIV)感染的靶细胞已得到充分证实,并且是艾滋病神经发病机制的主要促成因素。然而,尚未对携带病毒至脑部并在中枢神经系统(CNS)内持续感染的单核细胞/巨噬细胞不同亚群进行鉴定。我们证明,血管周围巨噬细胞而非实质小胶质细胞是被SIV有效感染的主要细胞。我们进一步证明,尽管CNS的有效病毒感染在早期就已发生,但在此之后,直到终末期艾滋病之前都难以检测到。血管周围巨噬细胞的生物学特性,包括其更新率以及被外周血单核细胞替代的情况,可能解释了病毒在CNS中神经侵袭、消失和再次出现的时间,并对大脑作为HIV/SIV有效感染储存库的能力提出了质疑。