Pre-transplant assessment of CMV-specific immune response by Elispot assay in kidney transplant recipients

被引:0
作者
Ritta, Massimo [1 ,2 ]
Costa, Cristina [1 ,2 ]
Sidoti, Francesca [1 ,2 ]
Balloco, Cinzia [1 ,2 ]
Ranghino, Andrea [3 ]
Messina, Maria [3 ]
Biancone, Luigi [3 ]
Cavallo, Rossana [1 ,2 ]
机构
[1] Univ Hosp Citta Salute & Sci Torino, SC Microbiol & Virol U, Turin, Italy
[2] Univ Turin, Dept Publ Hlth & Pediat, I-10126 Turin, Italy
[3] Univ Hosp Citta Salute & Sci Torino, Renal Transplantat Unit, Div Nephrol Dialysis & Transplantat, Dept Med Sci, Turin, Italy
关键词
Cytomegalovirus; Solid organ transplant; Immunosuppression; Kidney transplantation; Opportunistic infections; Cellular immune response; T-CELL RESPONSES; MEDIATED-IMMUNITY; ORGAN TRANSPLANT; CYTOMEGALOVIRUS; INFECTION; REPLICATION; RISK; PROTECTION; CONTRIBUTE; DISEASE;
D O I
暂无
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Cytomegalovirus (CMV) primary infection or re-activation in solid organ transplant (SOT) recipients is associated with increased morbidity and mortality, with patients with IgG-CMV D+/R- sero-matching at greater risk. The impact of pre-transplant CMV-specific host cellular immunity on the long-term risk of CMV replication in kidney transplants (KT) was prospectively evaluated in eighty patients by CMV-EliSpot assay. The study population included 54 male and 26 female recipients, with CMV-IgG distribution: 60 D+/R+, 11 D-/R+, 7 D+/R-, 2 D-/R-. At pre-transplantation, 49 KT (61.3%) were CMV-responders by EliSpot. At 3-month follow up, 16 (32.7%) out of 49 CMV-responders showed CMV blood infection, compared to 8 (25.8%) out of 31 non-responders. No further episode of CMV viraemia was reported in the responder group, in comparison to 15 out 31 non-responders (48.4%) showing at least one episode of CMV-DNAemia at 12-month follow-up. Baseline CMV-IgG serology showed a strong correlation with EliSpot determinations; KT recipients exhibiting at least one episode of CMV viraemia at 12-month follow-up showed lower baseline CMV-EliSpot values than those without signs of CMV replication. The study suggests that monitoring CMV-specific T-cell responses at pre-transplantation by EliSpot assay may be useful for predicting the post-transplantation risk of CMV infection and reactivation.
引用
收藏
页码:329 / 335
页数:7
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