The Immunobiogram, a novel in vitro diagnostic test to measure the pharmacodynamic response to immunosuppressive therapy in kidney transplant patients

被引:2
|
作者
Pascual, Julio [1 ,2 ]
Jimenez, Carlos [3 ]
Krajewska, Magdalena [4 ]
Seron, Daniel [5 ]
Kotton, Camille N. [6 ]
Portoles, Jose [7 ]
Witzke, Oliver [8 ]
Sorensen, Soren S. [9 ]
Andres, Amado [2 ]
Crespo, Marta [1 ]
Paz-Artal, Estela [10 ]
Diez, Teresa [11 ]
Ortega, Alvaro [11 ]
Portero, Isabel [11 ]
机构
[1] Hosp Mar, Inst Mar Med Res, Nephrol Dept, Barcelona, Spain
[2] Hosp 12 Octubre, Nephrol Dept, Madrid, Spain
[3] Hosp La Paz, Nephrol Dept, Madrid, Spain
[4] Wroclaw Med Univ, Dept Nephrol & Transplantat Med, Wroclaw, Poland
[5] Hosp Valle De Hebron, Nephrol Dept, Barcelona, Spain
[6] Massachusetts Gen Hosp, Transplant Infect Dis Div, Boston, MA 02114 USA
[7] Hosp Puerta Hierro, Nephrol Dept, Madrid, Spain
[8] Univ Duisburg Essen, Univ Hosp Essen, Dept Infect Dis, Essen, Germany
[9] Univ Hosp Copenhagen, Dept Nephrol, Rigshosp, Copenhagen, Denmark
[10] Hosp 12 Octubre, Immunol Dept, Madrid, Spain
[11] Biohope Sci Solut Human Hlth, Madrid, Spain
基金
欧盟地平线“2020”;
关键词
Transplant rejection; Immune cell assay; Cellular pharmacodynamics; immunosuppressive therapy monitoring; CYCLOSPORINE; MANAGEMENT; RECIPIENTS; REJECTION; CONSENSUS; FAILURE; DRUGS; DNA;
D O I
10.1016/j.trim.2022.101711
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: Diagnostic tools to measure the response to individual immunosuppressive drugs for transplant patients are currently lacking. We previously developed the blood-based Immunobiogram bioassay for in-vitro characterization of the pharmacodynamic response of patients' own immune cells to a range of immunosuppressants. We used Immunobiogram to examine the association between patients' sensitivity to their prescribed immunosuppressants and clinical outcome. Methods: We conducted an international, multicenter, observational study in a kidney transplant population undergoing maintenance immunosuppressive therapy. Patients were selected by clinical course poor [PCC] N = 53 (with renal dysfunction, and rejection signs in biopsy or/and an increase in DSA strength in last 12 months) versus good [GCC] N = 50 (with stable renal function and treatment, no rejection and no DSA titers). Immunobiogram dose-response curve parameters were compared between both subgroups in patients treated with mycophenolate, tacrolimus, corticosteroids, cyclosporine A or everolimus. Parameters for which significant inter-group differences were observed were further analyzed by univariate and subsequent multivariate logistic regression. Results: Clinical outcome was associated with following parameters: area over the curve (AOC) and 25% (ID25) and 50% (ID50) inhibitory response in mycophenolate, tacrolimus, and corticosteroid-treated subgroups, respectively. These statistically significant associations persisted in mycophenolate (OR 0.003, CI95% <0.001-0.258; p = 0.01) and tacrolimus (OR < 0.0001, CI95% <0.00001-0.202; p = 0.016) subgroups after adjusting for concomitant corticosteroid treatment, and in corticosteroid subgroup after adjusting for concomitant mycophenolate or tacrolimus treatment (OR 0.003; CI95% <0.0001-0.499; p = 0.026). Conclusions: Our results highlight the potential of Immunobiogram as a tool to test the pharmacodynamic response to individual immunosuppressive drugs.
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页数:9
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