نتایج جستجو برای: آنتی ژنمیا pp65

تعداد نتایج: 18147  

Journal: :Antimicrobial agents and chemotherapy 2001
C Gilbert J Roy R Belanger R Delage C Beliveau C Demers G Boivin

Fifty allogeneic stem cell transplant recipients were enrolled in a prospective cytomegalovirus pp65 antigenemia-guided preemptive therapy trial. Among these, 10 of 34 patients who received ganciclovir exhibited sustained and/or recurrent antigenemia despite treatment. Thirteen leukocyte preparations from these 10 subjects were screened for the presence of the most frequent cytomegalovirus UL97...

Journal: :Journal of Venomous Animals and Toxins including Tropical Diseases 2012

Journal: :Antimicrobial agents and chemotherapy 2014
Estela Giménez Carlos Solano José Ramón Azanza Paula Amat David Navarro

It is uncertain whether monitoring plasma ganciclovir (GCV) levels is useful in predicting cytomegalovirus (CMV) DNAemia clearance in preemptively treated allogeneic stem cell transplant recipients. In this observational study, including 13 episodes of CMV DNAemia treated with intravenous (i.v.) GCV or oral valganciclovir, we showed that monitoring trough plasma GCV levels does not reliably pre...

Journal: :The Journal of general virology 1999
D Zipeto B Bodaghi L Laurent J L Virelizier S Michelson

In permissive cells, human cytomegalovirus encodes the protein US28, a functional CC chemokine receptor. US28 polyadenylated mRNA could be detected by RT-PCR as early as 2 h post-infection. US28 mRNA appeared after major IE1 transcripts (UL123), but before transcripts of the early genes pp65 (UL83) and gB (UL55), and the late gene pp150 (UL32). This temporal appearance indicates that US28 is tr...

Journal: :The Journal of general virology 2008
Véronique Mersseman Katrin Besold Matthias J Reddehase Uwe Wolfrum Dennis Strand Bodo Plachter Sabine Reyda

Exogenous introduction of particle-associated proteins of human cytomegalovirus (HCMV) into the major histocompatibility complex (MHC) class I presentation pathway by subviral dense bodies (DB) is an effective way to sensitize cells against CD8 T-cell (CTL) recognition and killing. Consequently, these particles have been proposed as a platform for vaccine development. We have developed a strate...

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