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Differential effects of interleukin-13 on cytomegalovirus and human
immunodeficiency virus infection in human alveolar macrophages
WC Hatch, AR Freedman, DM Boldt-Houle, JE Groopman and EF Terwilliger
Division of Experimental Medicine, Beth Israel Deaconess Medical Center,
Harvard Medical School, Boston, MA 02215, USA.
Alveolar macrophages, which form a principal line of defense against a
variety of pulmonary pathogens, may themselves be infected by viruses like
human immunodeficiency virus-1 (HIV-1), which impair their defensive
functions. Interleukin-13 (IL-13), a multifunctional cytokine, has been
considered for therapeutic use based on its potent inhibition of HIV-1 in
these cells. We have further examined the effects of IL-13 on alveolar
macrophages under conditions that reflect those seen in acquired immune
deficiency syndrome, where this cell type is often infected by the
opportunistic pathogen human cytomegalovirus (HCMV). Alveolar macrophages
exposed to both HCMV and HIV-1 consistently exhibited higher levels of
HIV-1 replication than cells exposed to HIV-1 alone. HIV-1 production was
strongly suppressed in alveolar macrophages treated with IL-13 regardless
of whether or not the cultures were coinfected with HCMV. However, IL-13
treatment markedly enhanced the expression of HCMV in otherwise latently
infected macrophages in a dose dependent manner. These unexpected
differential effects of IL-13 on host-virus interactions are important
considerations in guiding its potential therapeutic applications.
Volume 89,
Issue 9,
pp. 3443-3450,
05/01/1997
Copyright © 1997 by The American Society of Hematology

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