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Human Cytomegalovirus-Specific T-Cell Immune Reconstitution in Preemptively Treated Heart Transplant Recipients Identifies Subjects at Critical Risk for Infection
Author(s) -
Davide Abate,
Marta Fiscon,
Alda Saldan,
Simona Cofano,
Carlo Mengoli,
Dino Sgarabotto,
Chiara d’Agostino,
Luisa Barzon,
Riccardo Cusinato,
Giuseppe Toscano,
Giuseppe Feltrin,
Antonio Gambino,
Gino Gerosa,
Giorgio Palù
Publication year - 2012
Publication title -
journal of clinical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.349
H-Index - 255
eISSN - 1070-633X
pISSN - 0095-1137
DOI - 10.1128/jcm.06406-11
Subject(s) - viremia , elispot , immune system , immunology , human cytomegalovirus , virology , cytomegalovirus , heart transplantation , transplantation , medicine , biology , t cell , viral disease , virus , herpesviridae
Human cytomegalovirus (CMV) infection represents a major threat for heart transplant recipients (HTXs). CMV-specific T cells effectively control virus infection, and thus, assessment of antiviral immune recovery may have clinical utility in identifying HTXs at risk of infection. In this study, 10 CMV-seropositive (R+ ) pretransplant patients and 48 preemptively treated R+ HTXs were examined before and after 100 days posttransplant. Preemptive treatment is supposed to favor the immune recovery. CMV DNAemia and gamma interferon enzyme-linked immunosorbent spot (ELISPOT) assay were employed to assess the viremia and immune reconstitution. HTXs could be categorized into three groups characterized by high (>100), medium (50 to 100), and low ( 4 log10 DNAemia/ml) was associated with a 36% decrease of the ELISPOT assay spot levels. All episodes of high viremia (>4 log10 DNAemia/ml) occurred from 1 to 60 days after transplant. Thus, the concomitant evaluation of viremia and CMV immune reconstitution has clinical utility in identifying HTXs at risk of infection and may represent a helpful guide in making therapeutic choices.

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