Dittmer D, Kedes D H
Department of Microbiology and Immunology, University of California, San Francisco, USA.
Bioessays. 1998 May;20(5):367-70. doi: 10.1002/(SICI)1521-1878(199805)20:5<367::AID-BIES3>3.0.CO;2-L.
Kaposi's sarcoma (KS) is an angiogenic tumor of mixed cellularity most commonly found in homosexual men infected with HIV. Both molecular and epidemiologic evidence has linked a newly described herpesvirus to this disease. This virus, Kaposi's sarcoma-associated herpesvirus (KSHV), encodes a number of cellular homologues, including two genes that share remarkable similarity to the human chemokine macrophage inhibitory factor-1 alpha. Recently, studies have begun to shed light on the roles these viral chemokines (vMIP-I and vMIP-II) may play in the complex pathogenesis of KS. The vMIP peptides may contribute to the formation of new blood vessels (neovascularization), inhibit infection by certain strains of HIV-1 and modify the cellular immune response.
卡波西肉瘤(KS)是一种细胞成分混合的血管生成性肿瘤,最常见于感染HIV的同性恋男性。分子和流行病学证据均已将一种新描述的疱疹病毒与该疾病联系起来。这种病毒,即卡波西肉瘤相关疱疹病毒(KSHV),编码多种细胞同源物,包括两个与人类趋化因子巨噬细胞抑制因子-1α具有显著相似性的基因。最近,研究已开始揭示这些病毒趋化因子(vMIP-I和vMIP-II)在KS复杂发病机制中可能发挥的作用。vMIP肽可能有助于新血管形成(新生血管化),抑制某些HIV-1毒株的感染,并改变细胞免疫反应。