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American Journal of Pathology, Vol 148, 1367-1373, Copyright © 1996 by American Society for Investigative Pathology
REGULAR ARTICLES |
N Tedla, P Palladinetti, M Kelly, RK Kumar, N DiGirolamo, U Chattophadhay, B Cooke, P Truskett, J Dwyer, D Wakefield and A Lloyd
Inflammation Research Unit, School of Pathology, University of New South Wales, Sydney, Australia.
Recruitment of T lymphocytes to lymph nodes in patients with HIV infection is critical to the pathogenesis of disease. Chemokines are a family of cytokines, which are potent regulators of leukocyte migration. We studied the leukocyte populations and expression of chemokines known to be active upon T cells in lymph nodes of four HIV infected patients and seven control subjects using in situ hybridization, immunohistochemistry, and FACS analysis. The HIV lymph nodes showed CD8+ T lymphocyte accumulation and strongly enhanced chemokine expression, notably for the CD8+ T cell chemoattractant, macrophage inflammatory protein (MIP)-1 alpha. Resident macrophages appeared to be a major cellular source of chemokines in the HIV nodes. RANTES expression was present in both HIV and control lymph nodes, suggesting a physiological role for this chemokine in T lymphocyte recirculation. Chemokines may be important determinants of T lymphocyte accumulation in lymphoid tissue of patients with HIV/AIDS.
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