Association of CMV-specific T-cell immunity and risk of CMV infection in lung transplant recipients
Autor: | Nikolaus Kneidinger, Teresa Kauke, Michael Zoller, Sebastian Michel, Christian Schneider, P Arnold, Bruno Meiser, Susanne Kunze, Jürgen Behr, Ming Pan, Andrea Dick, Dieter Munker, Julia Walter, Tobias Veit, Stephan H. Bohm |
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Rok vydání: | 2021 |
Předmět: |
medicine.medical_treatment
T-Lymphocytes Cytomegalovirus Viremia 030230 surgery Lower risk medicine.disease_cause Antiviral Agents 03 medical and health sciences 0302 clinical medicine Immunity medicine T cell immunity Lung transplantation Humans Lung Retrospective Studies Transplantation business.industry virus diseases medicine.disease Transplant Recipients medicine.anatomical_structure Immunology Cytomegalovirus Infections 030211 gastroenterology & hepatology business |
Zdroj: | Clinical transplantationREFERENCES. 35(6) |
ISSN: | 1399-0012 |
Popis: | Background Protecting against CMV infection and maintaining CMV in latent state are largely provided by CMV-specific T-cells in lung transplant recipients. The aim of the study was to assess whether a specific T-cell response is associated with the risk for CMV infection in seronegative patients who are at high risk for delayed CMV infection. Methods All CMV-seronegative recipients (R-) from CMV-seropositive donors (D+) between January 2018 and April 2019 were included and retrospectively screened for CMV infection before and after assessment of CMV-specific cell-mediated immunity. Results Thirty-one of the 50 patients (62%) developed early-onset CMV infection. Lower absolute neutrophil counts were significantly associated with early-onset CMV infection. Antiviral prophylaxis was ceased after 137.2 ± 42.8 days. CMV-CMI were measured at a median of 5.5 months after LTx. 19 patients experienced early and late-onset CMV infection after prophylaxis withdrawal within 15 months post transplantation. Positive CMV-CMI was significantly associated with lower risk of late-onset CMV infection after transplantation in logistic and cox-regression analysis (OR=0.05, p = .01; OR=2,369, p = .026). Conclusion D+/R- lung transplant recipients are at high risk of developing early and late-onset CMV infection. Measurement of CMV-CMI soon after transplantation might further define the CMV infection prediction risk in LTx recipients being at high risk for CMV viremia. |
Databáze: | OpenAIRE |
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