中华微生物学和免疫学杂志
中華微生物學和免疫學雜誌
중화미생물학화면역학잡지
CHINESE JOURNAL OF MICROBIOLOGY AND IMMUNOLOGY
2013年
7期
481-487
,共7页
段昭君%支玉红%龙璐%刘媛%许强%沈弢%鲁凤民
段昭君%支玉紅%龍璐%劉媛%許彊%瀋弢%魯鳳民
단소군%지옥홍%룡로%류원%허강%침도%로봉민
CD56+ T细胞%丙型肝炎%细胞毒效应%IFN-γ%TNF-α
CD56+ T細胞%丙型肝炎%細胞毒效應%IFN-γ%TNF-α
CD56+ T세포%병형간염%세포독효응%IFN-γ%TNF-α
CD56+T cells%Hepatitis C%Cytotoxic effect%IFN-γ%TNF-α
目的探讨慢性HCV感染者外周血中CD56+T细胞的频数、表型和体外细胞毒功能特征。方法采用流式细胞术检测33例慢性HCV感染者及21例健康对照者外周血CD56+T细胞的频数和细胞表面活化性受体NKG2C、CD16、NKp46和抑制性受体CD158a、NKG2A的表达水平;检测体外未刺激及K562细胞刺激作用下CD 56+T细胞毒效应( CD107a)和细胞因子分泌水平( IFN-γ和TNF-α),并分析上述3种CD56+T细胞功能指标之间的关联性。结果与健康对照相比,慢性HCV感染者外周血中CD56+T细胞在淋巴细胞中的比例明显降低( P=00.18)。 CD56+T细胞表面的活化性受体 NKG2C(P=0.015)、CD16(P=0.036)、NKp46(P=0.001)均有不同程度降低,而抑制性受体CD158a、NKG2A未发现有统计学意义的差异(P>0.05)。体外未刺激情况下,慢性HCV感染者CD56+T细胞分泌细胞因子IFN-γ和TNF -α均显著弱于健康对照组(P <0.0001);在K562细胞刺激作用下,慢性HCV感染者 CD56+T细胞CD107 a水平及分泌细胞因子IFN-γ和TNF-α均呈显著降低趋势( P<0.0001),且3种功能指标表达水平密切关联(r>0.80, P<0.0001)。结论慢性HCV感染者CD56+T 细胞频数降低,细胞毒能力和重要细胞因子分泌能力均明显减弱。该结果提示显著受损的CD56+T细胞功能可能与HCV慢性持续性感染有关。
目的探討慢性HCV感染者外週血中CD56+T細胞的頻數、錶型和體外細胞毒功能特徵。方法採用流式細胞術檢測33例慢性HCV感染者及21例健康對照者外週血CD56+T細胞的頻數和細胞錶麵活化性受體NKG2C、CD16、NKp46和抑製性受體CD158a、NKG2A的錶達水平;檢測體外未刺激及K562細胞刺激作用下CD 56+T細胞毒效應( CD107a)和細胞因子分泌水平( IFN-γ和TNF-α),併分析上述3種CD56+T細胞功能指標之間的關聯性。結果與健康對照相比,慢性HCV感染者外週血中CD56+T細胞在淋巴細胞中的比例明顯降低( P=00.18)。 CD56+T細胞錶麵的活化性受體 NKG2C(P=0.015)、CD16(P=0.036)、NKp46(P=0.001)均有不同程度降低,而抑製性受體CD158a、NKG2A未髮現有統計學意義的差異(P>0.05)。體外未刺激情況下,慢性HCV感染者CD56+T細胞分泌細胞因子IFN-γ和TNF -α均顯著弱于健康對照組(P <0.0001);在K562細胞刺激作用下,慢性HCV感染者 CD56+T細胞CD107 a水平及分泌細胞因子IFN-γ和TNF-α均呈顯著降低趨勢( P<0.0001),且3種功能指標錶達水平密切關聯(r>0.80, P<0.0001)。結論慢性HCV感染者CD56+T 細胞頻數降低,細胞毒能力和重要細胞因子分泌能力均明顯減弱。該結果提示顯著受損的CD56+T細胞功能可能與HCV慢性持續性感染有關。
목적탐토만성HCV감염자외주혈중CD56+T세포적빈수、표형화체외세포독공능특정。방법채용류식세포술검측33례만성HCV감염자급21례건강대조자외주혈CD56+T세포적빈수화세포표면활화성수체NKG2C、CD16、NKp46화억제성수체CD158a、NKG2A적표체수평;검측체외미자격급K562세포자격작용하CD 56+T세포독효응( CD107a)화세포인자분비수평( IFN-γ화TNF-α),병분석상술3충CD56+T세포공능지표지간적관련성。결과여건강대조상비,만성HCV감염자외주혈중CD56+T세포재림파세포중적비례명현강저( P=00.18)。 CD56+T세포표면적활화성수체 NKG2C(P=0.015)、CD16(P=0.036)、NKp46(P=0.001)균유불동정도강저,이억제성수체CD158a、NKG2A미발현유통계학의의적차이(P>0.05)。체외미자격정황하,만성HCV감염자CD56+T세포분비세포인자IFN-γ화TNF -α균현저약우건강대조조(P <0.0001);재K562세포자격작용하,만성HCV감염자 CD56+T세포CD107 a수평급분비세포인자IFN-γ화TNF-α균정현저강저추세( P<0.0001),차3충공능지표표체수평밀절관련(r>0.80, P<0.0001)。결론만성HCV감염자CD56+T 세포빈수강저,세포독능력화중요세포인자분비능력균명현감약。해결과제시현저수손적CD56+T세포공능가능여HCV만성지속성감염유관。
Objective To explore the cell frequency , phenotypes and in vitro cytotoxic effects of circulating CD56+T cells in the patients with chronic HCV infection .Methods Peripheral blood mononu-clear cells (PBMCs) were isolated from 33 patients with HCV chronic infection and 21 healthy subjects. Multi-color flow cytometry was used to analyze cell frequency , expressions of activating receptors ( NKG2C, CD16 and NKp46) and inhibitory receptors (NKG2A and CD158a) on CD56+T cells.The functional mark-er for cytotoxic effects (CD107a) on circulating CD56+T cells and their cytokines expression (IFN-γand TNF-α) with or without stimulation of K 562 human Leukemia cell line were also analyzed .Then the correla-tions among the expressing levels of CD 107 a, IFN-γand TNF-αwere investigated .Results The frequency of CD56+T cells in periphery lymphocytes were significantly decreased in the patients with chronic HCV in -fection as compared with that in healthy controls ( P=0.018 ).The expressions of activating receptors (NKG2C, CD16 and NKp46) on CD56+T cells from HCV infected patients were decreased (P=0.015 for NKG2C, P=0.036 for CD16 and P=0.001 for NKp46), while there was no significant change in the ex-pressions of inhibitory receptors (P>0.05 for both CD158a and NKG2A).The concentrations of IFN-γand TNF-αsecreted by CD56+T cells in the patients with chronic HCV infection were significantly decreased with or without K562 stimulation (P<0.0001).However, in the presence of K562 cells CD107a expression on CD56+T cells were sharply decreased in the patients (P<0.0001).In absence of K562 cells, there was no significant change in CD107a expression on CD56+T cells from patients and healthy controls (P>0.05). The expressions of CD107a, IFN-γand TNF-αwere closely related under the stimulation of K562(r>0.80, P<0.0001).Conclusion The frequency of CD56+T cells was reduced in patients with chronic HCV infec-tion.Moreover, cytotoxic effects and cytokines production mediated by CD 56+T cells were also significantly impaired, indicating that the dysfunction of circulating CD 56+T cells might be associated with the persist-ence of chronic HCV infection .