Volume 13 Issue 4
Jul.  2022
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Wang Ruolin, Li Han, Jia Ya'nan, et al. Changes and significance of lymphocyte subsets in recipients with acute rejection after liver transplantation[J]. ORGAN TRANSPLANTATION, 2022, 13(4): 509-515. doi: 10.3969/j.issn.1674-7445.2022.04.015
Citation: Wang Ruolin, Li Han, Jia Ya'nan, et al. Changes and significance of lymphocyte subsets in recipients with acute rejection after liver transplantation[J]. ORGAN TRANSPLANTATION, 2022, 13(4): 509-515. doi: 10.3969/j.issn.1674-7445.2022.04.015

Changes and significance of lymphocyte subsets in recipients with acute rejection after liver transplantation

doi: 10.3969/j.issn.1674-7445.2022.04.015
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  •   Objective  To evaluate the changes and significance of lymphocyte subsets in the recipients with acute rejection after liver transplantation.  Methods  The recipients presenting with acute rejection after liver transplantation were assigned into the rejection group (n=17), and their counterparts with stable liver function were allocated into the control group (n=17) according to the ratio of 1∶1 by propensity score matching method. The incidence of acute rejection after liver transplantation was analyzed, and the concentration of tacrolimus in the recipients was compared between two groups. The absolute value and proportion of lymphocyte subsets in peripheral blood were compared between two groups. The diagnostic value of lymphocyte subsets for acute rejection after liver transplantation was assessed by the receiver operating characteristic (ROC) curve. The absolute value and proportion of lymphocyte subsets in the rejection group were compared before and after treatment.  Results  Among 17 recipients in the rejection group, 4 cases developed acute rejection within postoperative 28 d, and 13 cases had acute rejection within postoperative 29-180 d. No significant difference was noted in the tacrolimus concentration between two groups (P=0.295). Compared with the control group, the proportions of peripheral blood T cells, CD4+T cells, B cells and natural killer (NK) T cells were significantly increased in the rejection group (all P < 0.05). The elevated proportion of NKT cells in the early stage after liver transplantation was an independent risk factor for acute rejection following liver transplantation[odds ratio (OR) 1.774, 95% confidence interval (CI) 1.059-2.971, P=0.029]. ROC curve analysis showed that the area under curve (AUC) of CD4+T cells, B cells and NKT cells was 0.76, 0.73 and 0.77, respectively. The AUC of combined use of CD4+T cells, B cells and NKT cells was 0.89, with a cut-off value of 0.69, sensitivity of 0.706 and specificity of 0.941. After corresponding treatment, all recipients were gradually recovered, and liver functions were eventually restored to normal in the rejection group. After treatment, the proportion of T cells, CD4+T cells, CD8+T cells and NK cells was significantly decreased (all P < 0.05).  Conclusions  The elevated proportion of NKT cells indicates an increased risk of acute rejection after liver transplantation. Combined use of CD4+T cells, B cells and NKT cells may deliver early detection and diagnosis of acute rejection after liver transplantation.

     

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  • [1]
    CUERVO FLOREZ M, BRUNER J, ZARRINPAR A. Progress and challenges in diagnosis and treatment of rejection following liver transplantation[J]. Curr Opin Organ Transplant, 2021, 26(6): 669-674. DOI: 10.1097/MOT.0000000000000924.
    [2]
    庄莉, 刘相艳. 肝移植受者围手术期管理及并发症预防与治疗[J]. 中华消化外科杂志, 2021, 20(10): 1037-1041. DOI: 10.3760/cma.j.cn115610-20210915-00459.

    ZHUANG L, LIU XY. Perioperative management and complications prevention and treatment of recipients in liver transplantation[J]. Chin J Dig Surg, 2021, 20(10): 1037-1041. DOI: 10.3760/cma.j.cn115610-20210915-00459.
    [3]
    中华医学会器官移植学分会. 中国肝移植免疫抑制治疗与排斥反应诊疗规范(2019版)[J]. 器官移植, 2021, 12(1): 8-14, 28. DOI: 10.3969/j.issn.1674-7445.2021.01.002.

    Branch of Organ Transplantation of Chinese Medical Association. Diagnosis and treatment specification for immunosuppressive therapy and rejection of liver transplantation in China (2019 edition)[J]. Organ Transplant, 2021, 12(1): 8-14, 28. DOI: 10.3969/j.issn.1674-7445.2021.01.002.
    [4]
    田倩川, 吴昌鸿, 徐亚男, 等. 2020年器官移植免疫学实验研究进展[J]. 器官移植, 2021, 12(2): 143-154. DOI: 10.3969/j.issn.1674-7445.2021.02.004.

    TIAN QC, WU CH, XU YN, et al. Experimental research progress on immunology of organ transplantation in 2020[J]. Organ Transplant, 2021, 12(2): 143-154. DOI: 10.3969/j.issn.1674-7445.2021.02.004.
    [5]
    LI H, LI XL, CAO S, et al. Decreased granzyme B+CD19+B cells are associated with tumor progression following liver transplantation[J]. Am J Cancer Res, 2021, 11(9): 4485-4499.
    [6]
    XU WL, WANG RL, LIU Z, et al. Granzyme B-producing B cells function as a feedback loop for T helper cells in liver transplant recipients with acute rejection[J]. Inflammation, 2021, 44(6): 2270-2278. DOI: 10.1007/s10753-021-01498-9.
    [7]
    MARINO J, GONZALEZ-NOLASCO B, WANG X, et al. Contrasting effects of B cell depletion on CD4+ and CD8+ memory T cell responses generated after transplantation[J]. Am J Transplant, 2020, 20(9): 2551-2558. DOI: 10.1111/ajt.15858.
    [8]
    LOUIS K, MACEDO C, BAILLY E, et al. Coordinated circulating T follicular helper and activated B cell responses underlie the onset of antibody-mediated rejection in kidney transplantation[J]. J Am Soc Nephrol, 2020, 31(10): 2457-2474. DOI: 10.1681/ASN.2020030320.
    [9]
    LEMERLE M, GARNIER AS, PLANCHAIS M, et al. CD45RC expression of circulating CD8+ T cells predicts acute allograft rejection: a cohort study of 128 kidney transplant patients[J]. J Clin Med, 2019, 8(8): 1147. DOI: 10.3390/jcm8081147.
    [10]
    SCHLÖßER HA, THELEN M, DIEPLINGER G, et al. Prospective analyses of circulating B cell subsets in ABO-compatible and ABO-incompatible kidney transplant recipients[J]. Am J Transplant, 2017, 17(2): 542-550. DOI: 10.1111/ajt.14013.
    [11]
    KOENIG A, CHEN CC, MARÇAIS A, et al. Missing self triggers NK cell-mediated chronic vascular rejection of solid organ transplants[J]. Nat Commun, 2019, 10(1): 5350. DOI: 10.1038/s41467-019-13113-5.
    [12]
    MONTGOMERY RA, LOUPY A, SEGEV DL. Antibody-mediated rejection: new approaches in prevention and management[J]. Am J Transplant, 2018, 18(Suppl 3): 3-17. DOI: 10.1111/ajt.14584.
    [13]
    Banff schema for grading liver allograft rejection: an international consensus document[J]. Hepatology, 1997, 25(3): 658-663. DOI: 10.1002/hep.510250328.
    [14]
    COZZI E, COLPO A, DE SILVESTRO G. The mechanisms of rejection in solid organ transplantation[J]. Transfus Apher Sci, 2017, 56(4): 498-505. DOI: 10.1016/j.transci.2017.07.005.
    [15]
    LIU D, LIU B, LIN C, et al. Imbalance of peripheral lymphocyte subsets in patients with ankylosing spondylitis: a Meta-analysis[J]. Front Immunol, 2021, 12: 696973. DOI: 10.3389/fimmu.2021.696973.
    [16]
    寇建涛, 李先亮, 朱继巧, 等. 自创免疫状态量化评分标准评估肝移植受者术后免疫状态的可行性分析[J]. 中华器官移植杂志, 2020, 41(6): 362-366. DOI: 10.3760/cma.j.cn421203-20191110-00407.

    KOU JT, LI XL, ZHU JQ, et al. Application of Mingdao immune score system for evaluating the immune status of liver transplant recipients[J]. Chin J Organ Transplant, 2020, 41(6): 362-366. DOI: 10.3760/cma.j.cn421203-20191110-00407.
    [17]
    王勤拯, 王峰, 朱晓丹. 外周血淋巴细胞亚群变化在肝移植术后患者早期感染中的意义[J]. 精准医学杂志, 2020, 35(4): 372-375. DOI: 10.13362/j.jpmed.202004022.

    WANG QZ, WANG F, ZHU XD. Significance of peripheral blood lymphocyte subsets in early infection after liver transplantation[J]. J Precis Med, 2020, 35(4): 372-375. DOI: 10.13362/j.jpmed.202004022.
    [18]
    叶林森, 张英才, 唐晖, 等. 长期生存的肝移植受者外周血免疫细胞分析[J]. 中华普通外科杂志, 2017, 32(6): 508-511. DOI: 10.3760/cma.j.issn.1007-631X.2017.06.014.

    YE LS, ZHANG YC, TANG H, et al. Peripheral blood immune cells in long-term survival patients after liver transplantation[J]. Chin J Gen Surg, 2017, 32(6): 508-511. DOI: 10.3760/cma.j.issn.1007-631X.2017.06.014.
    [19]
    SANNIER A, STROUMZA N, CALIGIURI G, et al. Thymic function is a major determinant of onset of antibody-mediated rejection in heart transplantation[J]. Am J Transplant, 2018, 18(4): 964-971. DOI: 10.1111/ajt.14595.
    [20]
    VAN BESOUW NM, YAN L, DE KUIPER R, et al. The number of donor-specific IL-21 producing cells before and after transplantation predicts kidney graft rejection[J]. Front Immunol, 2019, 10: 748. DOI: 10.3389/fimmu.2019.00748.
    [21]
    CHONG AS. B cells as antigen-presenting cells in transplantation rejection and tolerance[J]. Cell Immunol, 2020, 349: 104061. DOI: 10.1016/j.cellimm.2020.104061.
    [22]
    LI J, LUO Y, WANG X, et al. Regulatory B cells and advances in transplantation[J]. J Leukoc Biol, 2019, 105(4): 657-668. DOI: 10.1002/JLB.5RU0518-199R.
    [23]
    SAN SEGUNDO D, RODRIGO E, KISLIKOVA M, et al. Frequencies of circulating B-cell subpopulations before kidney transplantation identify patients at risk of acute rejection[J]. Transplant Proc, 2015, 47(1): 54-56. DOI: 10.1016/j.transproceed.2014.12.011.
    [24]
    ZHU J, ZENG Y, DOLFF S, et al. Granzyme B producing B-cells in renal transplant patients[J]. Clin Immunol, 2017, 184: 48-53. DOI: 10.1016/j.clim.2017.04.016.
    [25]
    GERTH E, MATTNER J. The role of adaptor proteins in the biology of natural killer T (NKT) cells[J]. Front Immunol, 2019, 10: 1449. DOI: 10.3389/fimmu.2019.01449.
    [26]
    黄莹, 孙煦勇. 自然杀伤细胞、自然杀伤T细胞及其在移植免疫中双重作用的研究进展[J]. 山东医药, 2020, 60(16): 92-95. DOI: 10.3969/j.issn.1002-266X.2020.16.026.

    HUANG Y, SUN XY. Research progress of natural killer cells, natural killer T cells and their dual role in transplantation immunity[J]. Shandong Med J, 2020, 60(16): 92-95. DOI: 10.3969/j.issn.1002-266X.2020.16.026.
    [27]
    SCHUETZ C, LEE KM, SCOTT R, et al. Regulatory B cell-dependent islet transplant tolerance is also natural killer cell dependent[J]. Am J Transplant, 2017, 17(6): 1656-1662. DOI: 10.1111/ajt.14265.
    [28]
    CHEN M, MOHTIZE M, MATTEÏ MF, et al. Reduced levels of both circulating CD4+CD25+CD127low/neg and CD4+CD8neg invariant natural killer regulatory T cells in stable heart transplant recipients[J]. Clin Exp Immunol, 2011, 163(1): 104-112. DOI: 10.1111/j.1365-2249.2010.04281.x.
    [29]
    ZWEIMAN B, ATKINS PC, BEDARD PM, et al. Corticosteroid effects on circulating lymphocyte subset levels in normal humans[J]. J Clin Immunol, 1984, 4(2): 151-155. DOI: 10.1007/BF00915049.
    [30]
    VACHER-COPONAT H, BRUNET C, MOAL V, et al. Tacrolimus/mycophenolate mofetil improved natural killer lymphocyte reconstitution one year after kidney transplant by reference to cyclosporine/azathioprine[J]. Transplantation, 2006, 82(4): 558-566. DOI: 10.1097/01.tp.0000229390.01369.4a.
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