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Volume 6

Journal of Infectious Diseases and Therapy

ISSN: 2332-0877

Infection Congress 2018

March 01-02, 2018

March 01-02, 2018 Berlin, Germany

5

th

International Congress on

INFECTIOUS DISEASES

Quantitative PCR system for detection of clinically relevant CMV infections in patients with

inflammatory bowel disease

Nils Wethkamp

Head of Molecular Diagnostics, Germany

S

everal lines of evidence indicate that cytomegalovirus infection can be substantially associated with onset of inflammatory

bowel disease, especially in patients who are refractory to immunosuppressive treatment. As cytomegalovirus is widely

spread in the population a quantitative detection system was generated which is suitable to differentiate clinically relevant

cytomegalovirus infection of the intestine from common latent cytomegalovirus. By using a quantitative real-time PCR

approach, cytomegalovirus viral load was evaluated in formalin fixed and paraffin embedded colon biopsy samples of 136

patients diagnosed with inflammatory bowel disease. Besides initial cytomegalovirus testing, the PCR system was also used

to monitor therapy response after antiviral treatment. Cytomegalovirus DNA was detected in 27% patients with varying viral

loads. Thereof, 13 patients (35%) received an antiviral treatment with 12 of them going into remission (92%). Later, five patients

displayed a relapse and three patients who agreed to restart antiviral treatment again showed positive therapy response. A

retrospective comparison of viral loads with antiviral therapy response revealed a threshold of 600 cytomegalovirus copies/105

cells as indicative for clinically relevant infection. Interestingly, we found that sensitivity of cytomegalovirus detection by

immunohistochemistry was insufficient to reliably identify antiviral therapy responders. In summary, quantitative real-time

PCR using formalin fixed biopsy samples is suitable for detection of cytomegalovirus infection in tissue samples of patients

with inflammatory bowel disease. Moreover, it allows the definition of a viral load threshold, predictive for clinical relevance

concerning antiviral therapy response

.

wethkamp@pathologie-vechta.de

J Infect Dis Ther 2018, Volume 6

DOI: 10.4172/2332-0877-C1-039