Use of antibodies neutralizing epithelial cell infection to diagnose patients at risk for CMV Disease after transplantation

被引:19
作者
Blanco-Lobo, P. [1 ]
Cordero, E. [1 ]
Martin-Gandul, C. [1 ]
Gentil, M. A. [2 ]
Suarez-Artacho, G. [3 ]
Sobrino, M. [4 ]
Aznar, J. [1 ]
Perez-Romero, P. [1 ]
机构
[1] Univ Seville, Inst Biomed Sevilla IBIS, Univ Hosp Virgen del Rocio, Unit Infect Dis Microbiol & Prevent Med,CSIC, Seville, Spain
[2] Hosp Univ Virgen del Rocio, Serv Nephrol, Seville, Spain
[3] Hosp Univ Virgen del Rocio, Hepatobiliary & Pancreat Surg & Hepat Transplant, Seville, Spain
[4] Hosp Univ Virgen del Rocio, Serv Cardiol, Seville, Spain
关键词
Cytomegalovirus; Antibodies neutralizing epithelial cell infection; Solid organ transplant patients; Immune monitoring; Preemptive therapy; HUMAN CYTOMEGALOVIRUS; MEDIATED-IMMUNITY; ENDOTHELIAL-CELLS; NATURAL INFECTION; CLINICAL UTILITY; RECIPIENTS; COMPLEX; FIBROBLASTS; MANAGEMENT; TROPISM;
D O I
10.1016/j.jinf.2016.02.008
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Although a CMV-specific T-cell response is associated with reduced risk for infection after transplantation, some patients still develop CMV disease. Thus, the characterization of additional parameters of the CMV-specific immune response that correlate with the control of CMV infection and disease and their use in defining thresholds that can be applied to clinical practice is of interest. Methods: In a cohort of high risk solid organ transplant recipients we characterized CMV-specific T-cell responses using intracellular cytokine staining upon stimulation with pp65 and IE-1 peptides, and levels of CMV-specific antibodies neutralizing infection in fibroblast (MRC-5) and epithelial (ARPE-19) cells using microneutralization assays. Results: Although patients with a positive (>= 0.25% CD8(+)CD69(+)IFN-gamma+) T-cell response were 6.4 fold more protected (OR 6.4, 95% CI 1.6-25.3; p < 0.001) from CMV infection than patients without a response, 2 (4.2%) patients developed disease. We defined a cut-off titer for epithelial cell neutralizing antibodies of >= 480 that correlated with disease protection. Thus, patients with a CMV-specific T-cell response and titers >= 480 were 14.2 fold more protected from CMV infection (OR 14.2, 95% CI 5-40.2; p < 0.001) and had no episodes of CMV disease. Conclusions: Our results indicate that antibodies neutralizing epithelial cell infection may have an important role in long-term protection. Quantification of antibodies neutralizing epithelial cells, in addition to the T-cell response, may be useful for identifying patients with lower risk for CMV disease. (C) 2016 The British Infection Association. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:597 / 607
页数:11
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