QuantiFERON CMV Test and CMV Serostatus in Lung Transplant: Stratification Risk for Infection, Chronic and Acute Allograft Rejection

Author:

Solidoro Paolo12ORCID,Sciarrone Federico1,Sidoti Francesca3,Patrucco Filippo4ORCID,Zanotto Elisa3,Boffini Massimo5,Rinaldo Rocco Francesco12,Bondi Alessandro6ORCID,Albera Carlo12ORCID,Curtoni Antonio6ORCID,Costa Cristina6ORCID

Affiliation:

1. Division of Respiratory Medicine, Cardiovascular and Thoracic Department, AOU Città della Salute e della Scienza di Torino, 10126 Torino, Italy

2. Medical Sciences Department, University of Turin, 10126 Torino, Italy

3. Division of Virology, Department of Public Health and Pediatrics, AOU Città della Salute e della Scienza di Torino, 10126 Torino, Italy

4. Respiratory Diseases Unit, Medical Department, AOU Maggiore della Carità di Novara, 28100 Novara, Italy

5. Cardiac Surgery Division, Surgical Sciences Department, AOU Città della Salute e della Scienza di Torino, University of Turin, 10126 Torino, Italy

6. Division of Virology, Department of Public Health and Pediatrics, AOU Città della Salute e della Scienza di Torino, University of Turin, 10126 Torino, Italy

Abstract

The QuantiFERON CMV (QCMV) test evaluates specific adaptive immune system activity against CMV by measuring IFN-γ released by activated CD8+ T lymphocytes. We aimed to evaluate the QCMV test as a predictive tool for CMV manifestations and acute or chronic lung allograft rejection (AR and CLAD) in lung transplant (LTx) patients. A total of 73 patients were divided into four groups based on donor and recipient (D/R) serology for CMV and QCMV assay: group A low-risk for CMV infection and disease (D−/R−); group B and C at intermediate-risk (R+), group B with non-reactive QCMV and group C with reactive QCMV; group D at high-risk (D+/R−). Group D patients experienced higher viral replication; no differences were observed among R+ patients of groups B and C. D+/R− patients had a higher number of AR events and group C presented a lower incidence of AR. Prevalence of CLAD at 24 months was higher in group B with a higher risk of CLAD development (OR 6.33). The QCMV test allows us to identify R+ non-reactive QCMV population as the most exposed to onset of CLAD. This population had a higher, although non-significant, susceptibility to AR compared to the R+ population with reactive QCMV.

Publisher

MDPI AG

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