Accumulation of MAC387+ macrophages in paracortical areas of lymph nodes in rhesus monkeys acutely infected with simian immunodeficiency virus

被引:21
作者
Otani, I
Mori, K
Terao, K
Doi, K
Akari, H
Yoshikawa, Y
机构
[1] Natl Inst Infect Dis, Tsukuba Primate Ctr, Tsukuba, Ibaraki 3050843, Japan
[2] Univ Tokyo, Fac Agr, Dept Vet Pathol, Bunkyo Ku, Tokyo 1138657, Japan
[3] Natl Inst Infect Dis, AIDS Res Ctr, Shinjuku Ku, Tokyo 1628640, Japan
[4] Univ Tokushima, Sch Med, Dept Virol, Tokushima 7708503, Japan
[5] Univ Tokyo, Fac Agr, Dept Biomed Sci, Bunkyo Ku, Tokyo 1138657, Japan
关键词
simian immunodeficiency virus; monocyte-macrophage; lymph node; plasmacytoid monocyte;
D O I
10.1016/S1286-4579(99)80515-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We investigated the histological features of lymph nodes, focusing on monocytes/macrophages, in rhesus monkeys (Macaca mulatta) acutely infected with simian immunodeficiency virus (SIV). In monkeys infected with a pathogenic SIV, SIV mac239, MAC387(+) newly blood-derived macrophages markedly increased in number at: paracortical areas at 11 to 14 days postinoculation, concomitant with the peak of the primary SIV antigenemia. The MAC387(+) macrophages densely gathered around high endothelial venules and formed cell clusters with CD3(+) T lymphocytes, tingible body macrophages, and plasmacytoid monocytes. In the cell clusters, CD3(+) T lymphocytes which closely adhered to the MAC387(+) macrophages enlarged in size, suggesting a histological manifestation of T-lymphocyte activation by macrophages. By 54 days postinoculation, when SIV antigenemia became undetectable, the MAC387(+) macrophages decreased in number and the cell cluster disappeared from paracortical areas, In contrast, the monkeys infected with a nef-deleted mutant of SIV mac239 showed lower levels of SIV antigenemia and lower numbers of MAC387(+) macrophages in paracortical areas than those infected with SIV mac239. These results indicate that MAC387(+) macrophages accumulate in paracortical areas for the period of the intense primary SIV antigenemia and may play an important role in activating naive T lymphocytes. (C) 1999 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:977 / 985
页数:9
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