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Pretransplant CD28 Biomarker (Levels of Expression and Quantification of Molecules per Cell) in Peripheral CD4+ T Cells Predicts Acute Rejection Episodes in Liver and Kidney Recipients
被引:2
|作者:
Boix, F.
[1
]
Bolarin, J. M.
[1
]
Eguia, J.
[1
]
Gonzalez-Martinez, G.
[1
]
De La Pena, J.
[5
]
Galian, J. A.
[1
]
Hernandez-Martinez, A. M.
[4
]
Moya-Quiles, M. R.
[1
]
Legaz, I.
[1
]
Campillo, J. A.
[1
]
Ramirez, P.
[3
]
Sanchez-Bueno, F.
[3
]
Garcia-Alonso, A. M.
[1
]
Pons, J. A.
[4
]
Minguela, A.
[1
]
Llorente, S.
[2
]
Muro, M.
[1
]
机构:
[1] Clin Univ Hosp, Virgen Arrixaca IMIB, Dept Immunol, Murcia, Spain
[2] Clin Univ Hosp, Virgen Arrixaca IMIB, Dept Nephrol, Murcia, Spain
[3] Clin Univ Hosp, Virgen Arrixaca IMIB, Dept Surg, Murcia, Spain
[4] Clin Univ Hosp, Virgen Arrixaca IMIB, Dept Digest Med, Murcia, Spain
[5] Clin Univ Hosp, Virgen Arrixaca IMIB, Dept Pathol, Murcia, Spain
关键词:
TRANSPLANTATION;
LYMPHOCYTES;
D O I:
10.1016/j.transproceed.2016.09.028
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. Acute rejection (AR) remains a significant cause of graft loss. Better approaches to predict AR are being investigated. Surface CD28 protein is essential for T-cell proliferation and survival as well as cytokine production. Patients and Methods. Pretransplant CD4(+)CD28(+) peripheral T cells were examined in 30 liver recipients (LRs) and 31 kidney recipients (KRs) by flow cytometry. Results. Pretransplant CD4(+)CD28(+) T cells in LRs were significantly lower in rejectors than nonrejectors (P = .002). Furthermore, the total number of CD28 molecules per cell in LRs (P = .02) as well as KRs (P = .047) was significantly lower in rejectors than non rejectors. The healthy group did not display differences when compared with patients with end-stage liver disease or renal failure; however, stratification analysis displayed higher levels of CD4(+)CD28(+) when compared with rejected LRs (P = .04) but not KRs. CD28 levels <41.94% were able to discriminate LRs at high risk of AR (P = .003). Similarly, a total number of CD28 molecules <= 8359 (P = .031) in LRs and <= 7669 (P = .046) in KRs correlated with high risk of AR. Conclusion. The preliminary results presented herein exhibit a fast and noninvasive method that assists clinicians to prevent AR by monitoring CD4(+)CD28(+) peripheral T cells.
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页码:2987 / 2989
页数:3
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