The pathogenesis of neurological dysfunction associated with human immunodeficiency (HIV)-1 infection is uncertain. However, the presence of macrophage infiltrates in the central nervous system is a key feature of HIV encephalitis and is correlated with HIV-associated dementia. Moreover, it has been demonstrated that HIV-infected monocyte/macrophages can produce toxic substances that may play a critical role in the development of HIV-associated dementia. However, the exact mechanisms responsible for HIV infection and leukocyte recruitment to the central nervous system remain speculative. Similar to HIV-infected patients, simian immunodeficiency virus (SIV)- infected macaque monkeys develop immunosuppression and acquired immune deficiency syndrome (AIDS)-related inflammatory disorders, including AIDS encephalitis. In this study, we demonstrate that encephalitic brain from SIV- infected animals has elevated immunohistochemical expression of the C-C chemokines, macrophage inflammatory protein-1α and -β, RANTES, and monocyte chemotactic protein-3, and the C-X-C chemokine interferon-inducible protein- 10. These findings suggest that one or all of these chemokines could be involved in leukocyte recruitment to the brain in SIV-infected macaque monkeys.
|Number of pages||9|
|Journal||American Journal of Pathology|
|Publication status||Published - 1 Nov 1996|