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Sustained impairment of human cytomegalovirus (HCMV)-specific CD4(+ )and CD8(+ )T cell response is responsible for recurrent episodes of disseminated HCMV infection in a D(+)R(- )hand transplant recipient

Human cytomegalovirus (HCMV) infection is the major viral complication in solid organ transplant recipients. Seronegative recipents (R(-)) of organs from seropositive donors (D(+)) appear to be at higher risk of developing symptomatic HCMV infection. To what extent systemic life-threatening complica...

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Detalles Bibliográficos
Autores principales: Baldanti, Fausto, Lucchini, Giovanna, Lilleri, Daniele, Lanzetta, Marco
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556316/
https://www.ncbi.nlm.nih.gov/pubmed/18798988
http://dx.doi.org/10.1186/1757-1626-1-155
Descripción
Sumario:Human cytomegalovirus (HCMV) infection is the major viral complication in solid organ transplant recipients. Seronegative recipents (R(-)) of organs from seropositive donors (D(+)) appear to be at higher risk of developing symptomatic HCMV infection. To what extent systemic life-threatening complications can be risked for non-life-saving transplant procedures? A case report describing successful treatment of repeated episodes of active HCMV infection in a D(+)R(- )hand recipient in the absence of HCMV-specific T-cell immunity is presented. In the attempt to save both the patient and the transplanted hand, a preemptive treatment strategy was adopted with the aim to boost the constitution of the virus-specific T-cell immune response and simultaneously avoid onset of disease. Careful monitoring of HCMV load in blood and HCMV-specific T-cell immunity guided administration of repeated courses of antiviral treatment and avoided emergence of HCMV-related symptoms. Following establishment of HCMV-specific CD4(+ )and CD8(+ )T-cell response, preemptive treatment was no longer required due to sustained HCMV disappearance from blood. The patient is now well, and his hand too. In conclusion, evaluation of virus-specific T-cell immunity is of crucial importance in D(+)R(- )transplant recipients and careful monitoring of HCMV-specific T cell mediated response should always parallel monitoring of HCMV load in transplant recipients.