Key result
Positive CMV-specific cell-mediated immunity was significantly associated with a lower risk of late-onset CMV infection after lung transplantation (OR 0.05, p=0.01).
Why the study?
Does positive CMV-specific cell-mediated immunity reduce the risk of CMV infection in CMV-seronegative lung transplant recipients from seropositive donors?
Cohort (n=50)
Does positive CMV-specific cell-mediated immunity reduce the risk of CMV infection in CMV-seronegative lung transplant recipients from seropositive donors?
Odds Ratio: 0.05
p-value: p=0.01
Measurement of CMV-specific cell-mediated immunity soon after lung transplantation can help predict the risk of late-onset CMV infection in high-risk seronegative recipients.
May support CMV-CMI testing for late-infection risk stratification in D+/R- lung recipients; hypothesis-generating pending prospective trials.
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.
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Veit et al. (2021) conducted a cohort in CMV infection in lung transplant recipients (n=50). Positive CMV-specific cell-mediated immunity (CMV-CMI) vs. Negative/lower CMV-CMI was evaluated on Late-onset CMV infection (OR 0.05, p=0.01). Positive CMV-specific cell-mediated immunity was significantly associated with a lower risk of late-onset CMV infection after lung transplantation (OR 0.05, p=0.01).
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