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慢加急性肝衰竭患者外周血CD8^+ T细胞中CXCR3的表达及意义 被引量:6

CXCR3 expression in peripheral CD8^+ T cells in acute-on-chronic liver failure and clinical relevance
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摘要 目的探讨慢加急性肝衰竭(ACLF)患者CD8+T细胞上趋化因子受体3(CXCR3)的表达及与转归的关系。方法选择22例ACLF患者、18例普通慢性乙型肝炎(CHB)患者和20例健康志愿者。入院初收集血样,流式细胞仪检测外周血CD8+T细胞上CXCR3的表达。结果 ACLF患者中12例存活。CHB患者CXCR3+CD8+T细胞计数(70.31±38.07)×106·L-1,明显高于健康志愿者的(34.26±22.30)×106·L-1和ACLF患者的(10.63±8.57)×106·L-1,差异有统计学意义(P<0.05)。CXCR3+CD8+T细胞数量与ln ALT、ln AST或总胆红素水平无明显相关性。存活的ACLF患者CXCR3+CD8+T细胞计数(14.40±9.35)×106·L-1,明显高于死亡患者的(6.10±4.78)×106·L-1,差异有统计学意义(P=0.021)。结论 ACLF患者外周血CXCR3+CD8+T细胞的计数下降,并且可能与转归相关。 Objective To investigate the CXC chemokine receptor(CXCR) -3 expression in CD8 ^+T cells in a- cute - on - chronic liver failure (ACLF) and the association with outcomes. Methods A total of 22 ACLF patients, 18 chronic hepatitis B (CHB) patients, and 20 healthy volunteers were enrolled. Blood samples were collected at the begin- ning of hospitalization for ACLF and CHB patients. CXCR3 expression on peripheral CD8^ + T cells was determined by flow cytometry. Results Twelve ACLF patients survived. CXCR3 ^+ CD8 ^+ T cell counts in CHB patients (70. 31 ± 38.07 × 10^6/L) were higher than those in healthy controls ( (34. 26 ± 22. 30) × 10^6/L) (P 〈 0. 05 ), and the latter were higher than those in ACLF patients ( (10. 63 ± 8.57) × 10^6/L) (P 〈 0. 05). The CXCR3 ^+ CD8 ^+ T cells counts were not associ- ated with ln( ALT), In( AST), or total serum bilirubin levels. Between survivors and deceased in ACLF patients, there were significant differences in CXCR3 ^+CD8 ^+ T cell counts ( ( 14.40 ± 9.35 ) vs (6. 10± 4. 78 ) × 10^6/L ; P = 0. 021 ). Conclusion The counts of peripheral CXCR3 ^+ CD8 ^+ T cells decreased significantly in ACLF, and it might be associated with, poor clinical outcomes.
出处 《广东医学》 CAS 北大核心 2015年第15期2356-2361,共6页 Guangdong Medical Journal
基金 广东省医学科研基金立项课题(编号:A2012643)
关键词 乙型肝炎 肝衰竭 调节性免疫 趋化因子受体3 hepatitis B virus liver failure adaptive immunity CXC chemokine receptor 3
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  • 1RUSSELL J Q, MORRISSETFE G J, WEIDNER M, et al. Liver damage preferentially results from CD8 + T cells triggered by high affinity peptide antigens[J]. J Exp Med, 1998, 188(6) : 1147 - 1157.
  • 2DUNN C, BRUNETTO M, REYNOLDS G, et al. Cytokines in- duced during chronic hepatitis B virus infection promote a pathway for NK cell - mediated liver damage [ J ]. J Exp Med, 2007, 204 (3) : 667 - 680.
  • 3LARRUBIA J R, CALVINO M, BENITO S, et al. The role of CCRS/CXCR3 expressing CD8 + cells in liver damage and viral control during persistent hepatitis C virus infection[ J]. J Hepatol, 2007, 47(5) : 632 -641.
  • 4QIN S, ROqq'MAN J B, MYERS P, et al. The chemokine recep- tors CXCR3 and CCR5 mark subsets of T cells associated with cer- tain inflammatory reactions [ J l. J Clin Invest, 1998, 101 (4) : 746 -754.
  • 5APOLINARIO A, MAJANO P L, ALVAREZ PIREZ E, et al. In- creased expression of T cell chemokines and their receptors in chro- nic hepatitis C: relationship with the histological activity of liver disease[ J]. Am J Gastroenterol, 2002, 97 ( 11 ) : 2861 - 2870.
  • 6BOISVERT J, KUNKEL E J, CAMPBELL J J, et al. Liver - infil- trating lymphocytes in end - stage hepatitis C virus : subsets, acti- vation status, and chemokine receptor phenotypes[J]. J Hepatol, 2003, 38(1): 67-75.
  • 7REHERMANN B, NASCIMBENI M. Immunology of hepatitis B virus and hepatitis C virus infection[J]. Nat Rev hnmunol, 2005, 5(3) : 215 -229.
  • 8SARIN S K, KUMAR A, ALMEIDA J A, et al. Acute-on- chronic liver failure : consensus recommendations of the Asian Pa- cific Association for the study of the liver (APASL) [ J]. Hepatol Int, 2009, 3 (1) : 269 -282.
  • 9ZOU Z, XU D, LI B, et al. Compartmentalization and its implica- tion for peripheral immunologieally - competent cells to the liver in patients with HBV - related acute - on - chronic liver failure[ J ]. Hepatol Res, 2009, 39(12) : 1198 - 1207.
  • 10KATOONIZADEH A, LALEMAN W, VERSLYPE C, et al. Early features of acute - on - chronic alcoholic liver failure: a prospec- tive cohort study[J]. Gut, 2010, 59(11): 1561 -1169.

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