TY - JOUR
T1 - Cytomegalovirus induction of tumor necrosis factor-α by human monocytes and mucosal macrophages
AU - Smith, Phillip D.
AU - Saini, Sarbjit S.
AU - Raffeld, Mark
AU - Manischewitz, Jody F.
AU - Wahl, Sharon M.
PY - 1992/11
Y1 - 1992/11
N2 - Cytomegalovirus (CMV) is a major cause of inflammatory organ disease in immunosuppressed persons. To elucidate the mechanisms of CMV-induced inflammation, we investigated whether tumor necrosis factor-α (TNF-α) was involved in the pathogenesis of CMV colitis in patients with AIDS. In in situ hybridization experiments, TNF-α mRNA was shown to be abundantly present in colonic mucosa from AIDS patients with CMV colitis but not in colonic mucosa from control (AIDS and normal) subjects. The TNF-α transcripts, identified in macrophage-like cells containing cytomegalic inclusions, were positively associated with CMV, but not HIV-1, within the mucosa. In in vitro experiments, a patient-derived isolate of CMV, but not HIV-1Ba-L, induced human monocytes to express TNF-α mRNA and to release increased levels of TNF-α peptide following stimulation. CMV induction of TNF-α may play a critical role in CMV-induced inflammation and, since TNF-α upregulates expression of HIV-1, offers a mechanism by which CMV could serve as a co-factor for HIV-1 expression without both viruses infecting the same cell.
AB - Cytomegalovirus (CMV) is a major cause of inflammatory organ disease in immunosuppressed persons. To elucidate the mechanisms of CMV-induced inflammation, we investigated whether tumor necrosis factor-α (TNF-α) was involved in the pathogenesis of CMV colitis in patients with AIDS. In in situ hybridization experiments, TNF-α mRNA was shown to be abundantly present in colonic mucosa from AIDS patients with CMV colitis but not in colonic mucosa from control (AIDS and normal) subjects. The TNF-α transcripts, identified in macrophage-like cells containing cytomegalic inclusions, were positively associated with CMV, but not HIV-1, within the mucosa. In in vitro experiments, a patient-derived isolate of CMV, but not HIV-1Ba-L, induced human monocytes to express TNF-α mRNA and to release increased levels of TNF-α peptide following stimulation. CMV induction of TNF-α may play a critical role in CMV-induced inflammation and, since TNF-α upregulates expression of HIV-1, offers a mechanism by which CMV could serve as a co-factor for HIV-1 expression without both viruses infecting the same cell.
KW - AIDS
KW - Cytomegalovirus
KW - HIV
KW - Tumor necrosis factor
UR - http://www.scopus.com/inward/record.url?scp=0026438976&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0026438976&partnerID=8YFLogxK
M3 - Article
C2 - 1331170
AN - SCOPUS:0026438976
SN - 0021-9738
VL - 90
SP - 1642
EP - 1648
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
IS - 5
ER -