Efficacy of Valganciclovir Administered as Preemptive Therapy for Cytomegalovirus Disease in Liver Transplant Recipients: Impact on Viral Load and Late-Onset Cytomegalovirus Disease

2005 ◽  
Vol 79 (1) ◽  
pp. 85-90 ◽  
Author(s):  
Nina Singh ◽  
Cheryl Wannstedt ◽  
Lois Keyes ◽  
Timothy Gayowski ◽  
Marilyn M. Wagener ◽  
...  
Author(s):  
Nina Singh ◽  
Drew J Winston ◽  
Raymund R Razonable ◽  
G Marshall Lyon ◽  
Fernanda P Silveira ◽  
...  

Abstract Background Detailed CMV kinetics in donor CMV-seropositive, recipient CMV-seronegative (D+R-) transplant recipients receiving preemptive therapy (PET) have not been fully defined. Methods The study population consisted of PET arm of a randomized CMV prevention trial in D+R- liver transplant recipients. CMV-DNA PCR assays were performed weekly for 100 days using a sensitive assay. Viral load and clinical parameters were compared for patients with or without high-level increase (defined as higher than the group median log10 increase in viral load from baseline after PET initiation). Results Among 79 patients, 93.6% (74/79) developed an increase from baseline viral loads of median 120 IU/mL to 3,350 IU/mL; 25.7% (19/74) of the patients had peak levels > 10,000 IU/mL. None of the patients with rise in viral load underwent testing for CMV resistance and viremia resolved with PET with valganciclovir. Patients with high-level increase in viral load had significantly lower rate of recurrent viremia than those without such increase (40%,16/40 vs. 71.8%, 28/39, p=0.004), respectively. Conclusions A majority of D+R- recipients had a marked increase in viral load after initiation of PET before resolution of viremia. This phenomenon is associated with lower rates of subsequent recurrent viremia and does not necessarily imply antiviral resistance.


2012 ◽  
Vol 18 (9) ◽  
pp. 1093-1099 ◽  
Author(s):  
Marta Bodro ◽  
Núria Sabé ◽  
Laura Lladó ◽  
Carme Baliellas ◽  
Jordi Niubó ◽  
...  

2004 ◽  
Vol 78 (9) ◽  
pp. 1390-1396 ◽  
Author(s):  
Ajit P. Limaye ◽  
Ramaswamy Bakthavatsalam ◽  
Hyung W. Kim ◽  
Christian S. Kuhr ◽  
Jeffrey B. Halldorson ◽  
...  

2019 ◽  
Vol 220 (5) ◽  
pp. 752-760 ◽  
Author(s):  
Ajit P Limaye ◽  
Margaret L Green ◽  
Bradley C Edmison ◽  
Terry Stevens-Ayers ◽  
Sam Chatterton-Kirchmeier ◽  
...  

Abstract The differential impact of preemptive therapy (PET) and antiviral prophylaxis (AP) on development of cytomegalovirus (CMV)–specific neutralizing antibody (nAb) and T-cell responses have not previously been directly compared in high-risk donor-seropositive/recipient-seronegative (D+R−) organ transplant recipients. We prospectively assessed T-cell and nAb responses 3 months after transplantation in cohorts of high-risk D+R− liver transplant recipients who received either PET (n = 15) or AP (n = 25) and a control group of CMV-seropositive transplant recipients (R+) (AP; n = 24). CMV phosphoprotein 65 (pp65)– and immediate early protein 1–specific multifunctional T-cell responses were determined by means of intracellular cytokine staining and nAbs against BADrUL131-Y4 CMV in adult retinal pigment epithelial cell line-19 human epithelial cells; nAbs were detected in 8 of 12 (67%) in the PET group, none of 17 in the AP group, and 20 of 22 (91%) in the R+ group. Multifunctional CD8 and CD4 T-cell responses to pp65 were generally similar between PET and R+ groups, and lower for the AP group; multifunctional CD4 responses were similar across all groups. Among D+R− liver transplant recipients, PET was associated with the development of greater nAb and multifunctional CD8 T-cell responses compared with AP, providing a potential mechanism to explain the relative protection against late-onset disease with PET. Future studies are needed to define specific immune parameters predictive of late-onset CMV disease with AP.


JAMA ◽  
2020 ◽  
Vol 323 (14) ◽  
pp. 1378 ◽  
Author(s):  
Nina Singh ◽  
Drew J. Winston ◽  
Raymund R. Razonable ◽  
G. Marshall Lyon ◽  
Fernanda P. Silveira ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document