Your browser doesn't support javascript.
loading
Cytomegalovirus induction of tumor necrosis factor-alpha by human monocytes and mucosal macrophages.
Smith, P D; Saini, S S; Raffeld, M; Manischewitz, J F; Wahl, S M.
Afiliação
  • Smith PD; Cellular Immunology Section, National Institute of Dental Research, National Institutes of Health, Bethesda, Maryland 20892.
J Clin Invest ; 90(5): 1642-8, 1992 Nov.
Article em En | MEDLINE | ID: mdl-1331170
ABSTRACT
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-alpha (TNF-alpha) was involved in the pathogenesis of CMV colitis in patients with AIDS. In in situ hybridization experiments, TNF-alpha 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-alpha 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-alpha mRNA and to release increased levels of TNF-alpha peptide following stimulation. CMV induction of TNF-alpha may play a critical role in CMV-induced inflammation and, since TNF-alpha 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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Monócitos / Fator de Necrose Tumoral alfa / Citomegalovirus / Mucosa Intestinal / Macrófagos Tipo de estudo: Prognostic_studies Limite: Humans / Male Idioma: En Revista: J Clin Invest Ano de publicação: 1992 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Monócitos / Fator de Necrose Tumoral alfa / Citomegalovirus / Mucosa Intestinal / Macrófagos Tipo de estudo: Prognostic_studies Limite: Humans / Male Idioma: En Revista: J Clin Invest Ano de publicação: 1992 Tipo de documento: Article