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慢性肾功衰竭患者免疫功能紊乱的效应体CD23分子的表达与调控 被引量:1

IMMUNE DYSREGULATION IN CHRONIC UREMIA: EXPRESSION OF CD23 ANTIGEN AND ITS REGULATION BY IL4 AND IFNγ
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摘要 目的:研究慢性肾功能衰竭(CRF)患者免疫功能紊乱的效应体CD23分子的表达与调控。方法:利用细胞培养和间接免疫荧光技术,比较了CRF患者与正常人外周血B细胞膜CD23的表达,并研究重组人白介素4(rhIl-4)和重组人γ干扰素(rHIFN-γ)对CD23的调控作用。结果:CRF患者外周血CD23+B细胞较正常人显著增高;IL-4能促进CRF患者和正常人B细胞CD23的表达;IFN-γ可显著抑制IL-4诱导的B细胞CD23的表达。结论:CRF患者存在B细胞的激活;CRF患者和正常人一样,外周血B细胞CD23表达受IL-4上调和IFN-γ下调影响;CD23分子不仅是CRF患者免疫功能紊乱的效应体,而且可能参与这些患者免疫紊乱的发病机理。 OBJECTIVE To study the expression of CD23 antigen and its regulation in patients with chronic renal failure(CRF).METHODOLOGY CD23 was investigated on peripheral blood B lymphocyte from CRF patients and normal donors by indirect immunofluorescence assay, and the influence of rhIL4 and rhIFNγ on its expression was examined.RESULTS (1) The CD23 expression was significantly higher on the B cells from CRF patients (48.81±12.57%) than on the B cells of healthy donors (the control)(16.20±5.08%)(P<0.001); (2) rhIL4 increased CD23 expression on the control (from 16.39±5.09% to 39.29±8.10%, P<0.05) and the CRF B cells(from 59.12±7.94% to 75.35±9.98%, P<0.05); (3) rhIFNγ specifically inhibited the rhIL4 mediated induction of CD23 expression on the control (from 39.29±8.10% to 18.0±3.31%, P<0.05) and on the CRF B cells (from 75.35±9.98% to 30.38±7.89%, P<0.001).CONCLUSION Uremic patients may have a B cell activation state in basal conditions. CD23 expression on B cell of CRF patients was upregulated by IL4 and downregulated by IFNγ. CD23 may not only be an effector of immune dysregulation in CRF, but also act as a costimulatory factor in the T cell activation associated with chronic uremia.
出处 《肾脏病与透析肾移植杂志》 CAS CSCD 1997年第6期546-549,共4页 Chinese Journal of Nephrology,Dialysis & Transplantation
关键词 慢性 肾功能衰竭 CD23 免疫功能紊乱 chronic renal failure CD23 rhIL4 rhIFNγ
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  • 1Raska K, Rankova J, Shea SM, et al.T cell subsets and cellular immunity in renal disease. Am J Med 1998; 75:734 被引量:1
  • 2Cella M, Sallusto F, Lanzavecchia A. Origin, maturation and antigen presenting function of dendritric cells. Current Opin Immunol 1997; 9:10 被引量:1
  • 3Thomams RM. The dendritic cells:origin and differentiation. Stem Cell 1996; 14:271 被引量:1
  • 4Ringoir SMC, Van Landschoot N, De Smet R. Inhibition of phagoctosis by a middle molecular fraction from ultrafilter. Clin Nephrol 1999; 13:109 被引量:1
  • 5Klinger M, Alexiewica JM, Linker M, et al. Effect of parathyroid hormone on human T cell antivation. Kidney Int 1998; 37:1543 被引量:1
  • 6孙劲旅,张锦.树突状细胞与T、B细胞相互关系研究进展[J].国外医学(免疫学分册),1999,22(4):215-218. 被引量:4

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