Cytomegalovirus Replication Kinetics in Solid Organ Transplant Recipients Managed by Preemptive Therapy

Sowsan Atabani(University College London), Colette Smith(Biology of Infection), Claire Atkinson(Institute of Infection and Immunity), Robert W Aldridge(National Centre for Infectious Diseases), Manuel Rodríguez‐Perálvarez(The Royal Free Hospital), Nancy Rolando(The Royal Free Hospital), Mark Harber(The Royal Free Hospital), Gareth Jones(University College London), Alan O’Riordan(University College London), Andrew K. Burroughs(The Royal Free Hospital), Douglas Thorburn(University College London), James O’Beirne(The Royal Free Hospital), R Milne(Institute of Infection and Immunity), Vincent C. Emery(Institute of Infection and Immunity), Paul Griffiths(Institute of Infection and Immunity)
American Journal of Transplantation
May 17, 2012
Cited by 219Open Access
Full Text

Abstract

After allotransplantation, cytomegalovirus (CMV) may be transmitted from the donor organ, giving rise to primary infection in a CMV negative recipient or reinfection in one who is CMV positive. In addition, latent CMV may reactivate in a CMV positive recipient. In this study, serial blood samples from 689 kidney or liver transplant recipients were tested for CMV DNA by quantitative PCR. CMV was managed using preemptive antiviral therapy and no patient received antiviral prophylaxis. Dynamic and quantitative measures of viremia and treatment were assessed. Median peak viral load, duration of viremia and duration of treatment were highest during primary infection, followed by reinfection then reactivation. In patients who experienced a second episode of viremia, the viral replication rate was significantly slower than in the first episode. Our data provide a clear demonstration of the immune control of CMV in immunosuppressed patients and emphasize the effectiveness of the preemptive approach for prevention of CMV syndrome and end organ disease. Overall, our findings provide quantitative biomarkers which can be used in pharmacodynamic assessments of the ability of novel CMV vaccines or antiviral drugs to reduce or even interrupt such transmission.


Related Papers

No related papers found

Powered by citation graph analysis