Evaluation of Cytomegalovirus (CMV)-Specific T Cell Immune Reconstitution Revealed That Baseline Antiviral Immunity, Prophylaxis, or Preemptive Therapy but not Antithymocyte Globulin Treatment Contribute to CMV-Specific T Cell Reconstitution in Kidney Transplant Recipients

被引:96
作者
Abate, Davide [1 ]
Saldan, Alda [1 ]
Fiscon, Marta [1 ]
Cofano, Simona [1 ]
Paciolla, Adriana [3 ]
Furian, Lucrezia [2 ]
Ekser, Burcin [2 ]
Biasolo, Maria Angela [1 ]
Cusinato, Riccardo [1 ]
Mengoli, Carlo [1 ]
Bonfante, Luciana [3 ]
Rossi, Barbara [4 ]
Rigotti, Paolo [2 ]
Sgarabotto, Dino [5 ]
Barzon, Luisa [1 ]
Palu, Giorgio [1 ]
机构
[1] Univ Padua, Dept Histol Microbiol & Med Biotechnol, Padua Gen Hosp, Sch Med, I-35121 Padua, Italy
[2] Univ Padua, Dept Gen Surg & Solid Organ Transplantat, Padua Gen Hosp, Sch Med, I-35121 Padua, Italy
[3] Univ Padua, Dept Surg & Med Sci Nephrol 1, Padua Gen Hosp, Sch Med, I-35121 Padua, Italy
[4] Univ Padua, Dept Hemodialysis & Nephrol 2, Padua Gen Hosp, Sch Med, I-35121 Padua, Italy
[5] Univ Padua, Transplant Infect Dis Unit, Padua Gen Hosp, Sch Med, I-35121 Padua, Italy
关键词
SOLID-ORGAN; INFECTION; DISEASE; RESPONSES; RISK; SIROLIMUS; OUTCOMES;
D O I
10.1086/654931
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The ultimate goal of organ transplantation is the reestablishment of organ function and the restoration of a solid immunity to prevent the assault of potentially deadly pathogens. T cell immunity is crucial in controlling cytomegalovirus (CMV) infection. It is still unknown how preexisting antiviral T cell levels, prophylaxis, or preemptive antiviral strategies and pharmacological conditioning affect immune reconstitution. Methods. Seventy preemptively treated CMV-seropositive recipients, 13 prophylaxis-treated CMV-seronegative recipients of seropositive donor transplants, 2 seropositive recipients of seronegative donor kidneys, and 27 pre-transplant subjects were enrolled in a cross-sectional study and analyzed for CMV viremia (DNAemia) and CMV-specific T cell response (interferon-gamma enzyme-linked immunospot assay) before transplantation and at 30, 60, 90, 180, and 360 days after transplantation. Results. CMV-seropositive transplant recipients displayed a progressive but heterogeneous pattern of immune reconstitution starting from day 60 after transplantation. CMV-seronegative recipients did not mount a detectable T cell response throughout the prophylaxis regimen. A single episode of CMV viremia (CMV copy number, 7000-170,000 copies/mL) was sufficient to prime a protective T cell immune response in CMV-seronegative recipients. Antithymocyte globulin treatment did not significantly affect CMV-specific T cell response. Conclusions. Baseline immunity, antiviral therapy but not antithymocyte globulin treatments profoundly influence T cell reconstitution in kidney transplant recipients.
引用
收藏
页码:585 / 594
页数:10
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