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1.
妊娠高血压综合征免疫学发病机制的研究   总被引:2,自引:0,他引:2  
目的:研究妊娠高血压综合征(妊高征)的免疫学发病机制。方法:通过检测妊高征患者及正常孕妇蜕膜组织细胞培养上清液中白细胞介素-1(IL-1)、白细胞介素-2(IL-2)和肿瘤坏死因子-α(TNF-α)的活性,分析蜕膜免疫细胞因子的变化与妊高征之间的关系。结果:与正常孕妇相比,妊高征患者蜕膜组织中IL-1、IL-2和TNF-α的分泌显著升高。结论:蜕膜组织免疫微环境中细胞因子的改变可能是妊高征发病的机制之一  相似文献   

2.
妊娠高血压综合征患者白细胞介素18和内皮素1的变化研究   总被引:1,自引:1,他引:1  
目的 探讨妊娠高血压综合征 (简称妊高征 )患者白细胞介素 18(IL - 18)的变化及与内皮素 1(ET- 1)的相关性。 方法 用夹心酶联免疫法 (EL ISA法 )检测妊高征患者 47例 (妊高征组 )和正常孕妇 30例 (正常妊娠组 )血清 IL - 18含量 ,同时用放射免疫法检测血浆 ET- 1含量。 结果 (1)血清 IL - 18水平妊高征组 (M=43.76 ng/ L )明显高于正常妊娠组 (M=37.97ng/ L ) ,H =42 .845 ,P<0 .0 5 ;血浆 ET- 1含量妊高征组 (6 1± 2 3) ng/ L明显高于正常妊娠组 (35± 11) ng/ L ,F=2 4.5 80 ,P<0 .0 5 ,病情越重其值越高。 (2 )妊高征组血清 IL - 18值与血浆 ET- 1值呈正相关关系 (r=0 .6 773,P<0 .0 1)。 结论  IL - 18可能参与妊高征免疫损伤过程 ,其变化与 ET- 1呈正相关关系 ,推测可能是IL - 18的变化 ,损伤了血管内皮 ,使 ET- 1合成释放增加 ,而导致妊高征的发生。  相似文献   

3.
目的 探讨妊娠高血压综合征 (妊高征 )患者胎盘和脐带血管内皮细胞损伤及功能变化与肿瘤坏死因子 (TNF)的关系。方法 采用放射免疫分析法 ,测定 41例妊高征患者 (妊高征组 )和 35例正常妊娠妇女 (对照组 )血浆TNF、内皮素和一氧化氮的水平 ;采用透射电镜观察两组胎盘和脐带血管内皮细胞的超微结构 ,并与在体外人重组TNF(rTNF)作用下培养的脐带血管内皮细胞形态相比较。结果  (1)妊高征组血浆TNF和内皮素分别为 (2 .2 7± 0 .42 ) μg/L和 (73.31± 9.98)ng/L ,一氧化氮为(10 4.93± 2 0 .5 4) μmol/L ;对照组血浆TNF和内皮素分别为 (1.72± 0 .2 5 ) μg/L和 (5 2 .32± 10 .44 )ng/L ,一氧化氮水平为 (138.2 5± 2 2 .16 ) μmol/L。妊高征组TNF及内皮素增高 ,一氧化氮减少。两组比较 ,差异有显著性 (P <0 .0 5 )。(2 )电镜显示 ,妊高征组中除轻度患者的胎盘及脐带血管未见异常改变外 ,中、重度患者的胎盘和脐带血管内皮细胞均有损伤性表现。与rTNF作用下于体外培养的脐带血管内皮细胞形态学的改变相似。结论 TNF可引起胎盘和脐带血管内皮细胞损伤 ,可导致血管调节因子失衡 ,在妊高征的发病中有一定作用。  相似文献   

4.
妊高征孕妇血浆肿瘤坏死因子水平变化的初步观察   总被引:2,自引:0,他引:2  
妊高征孕妇血浆肿瘤坏死因子水平变化的初步观察刘锦霞冷雯陆康民苏延华妊高征是危害母婴健康的常见病之一,其病因未明。近年来发现,细胞因子可能在妊高征发病中起重要作用。本研究采用放射免疫法测定正常晚期妊娠及妊高征妇女血浆肿瘤坏死因子(TNF-α)水平,以探...  相似文献   

5.
目的:探讨早产儿及足月儿出生时免疫功能的变化。方法:采用细胞原位杂交技术,对早产儿16例(观察组)和足月儿18例(对照组)出生时脐血的白细胞介素-1β(IL-1β)和白细胞介素-1受体拮抗剂(IL-1rα)基因表达水平进行分析。结果:观察组中,胎膜早破自娩的新生儿IL-1β和IL-1rα的mRNA表达明显低于观察组中妊高征剖宫产新生儿和对照组(P<0.001)。而观察组中妊高征剖宫产新生儿IL-1β和IL-1rα的mRNA表达与对照组之间,差异无显著性。结论:脐血中IL-1β和IL-1rα的表达可能与胎儿成熟度有关。  相似文献   

6.
目的:探讨大颗粒淋巴细胞(LGLs)和肿瘤坏死因子-α(TNF-α)与妊高征发病的关系。方法:应用双抗体夹心酶联免疫吸附法(ELISA)、全血细胞分析仪结合油镜下计数LGLs占淋巴细胞的百分数检测妊高征39例(妊高征组),正常孕晚期40例(正常妊娠组)和健康育龄非妊娠40例(对照组)外周血TNF-α含量和LGLs数量。结果:妊高征组外周血LGLs和TNF-α水平高于正常妊娠组、对照组,以中、重度妊高征患者增高最为显著(P<0.05),其中合并胎儿宫内生长迟缓(IUGR)者外周血LGLs和TNF-α水平与未合并IUGR者差异无显著性(P>0.05)。结论:细胞免疫,特别是LGLs和TNF-α参与了妊高征的病理机制,妊高征发病与异常免疫激活有关  相似文献   

7.
目的 探讨沙眼衣原体 (CT)感染所致输卵管性不孕患者输卵管液中肿瘤坏死因子α(TNF α)和白细胞介素 6 (IL 6 )的水平及其意义。方法 用酶联免疫吸附试验法测定 2 2例CT感染输卵管性不孕 (A组 )、2 3例非CT感染输卵管性不孕 (B组 )及 19例已生育输卵管正常妇女 (对照组 )输卵管液中TNF α和IL 6的水平。结果 A组TNF α的水平为 178ng/L ,高于对照组的 12 4ng/L(P<0 .0 1) ;A组中输卵管阻塞者TNF α为 199ng/L ,高于粘连者的 142ng/L(P <0 .0 1)。A组IL 6的水平为 6 81ng/L ,高于B组的 2 6 4ng/L及对照组的 2 2 9ng/L(P均 <0 .0 1) ,B组与对照组之间比较差异无显著性 (P >0 .0 5 )。结论 无症状输卵管CT感染可使输卵管液中TNF α和IL 6升高 ,其中TNF α与输卵管损伤程度有关。TNF α越高 ,损伤越重  相似文献   

8.
目的 探讨可溶性细胞间粘附分子 1(soluble intercellular adhesion molecule- 1,s ICAM- 1)在妊娠高血压综合征 (简称妊高征 )发病中的作用。 方法 应用酶联免疫吸附法 (EL ISA)测定 6 5例妊高征患者 (妊高征组 ,包括轻度 15例 ,中度 2 4例 ,重度 2 6例 )及 2 5例同期正常妊娠孕妇(对照组 )外周血清中 s ICAM- 1的含量 ;应用化学发光酶联免疫分析法测定两组孕妇血清中白细胞介素 1(interleukin- 1,L I- 1β)及肿瘤坏死因子 (tum or necrosing factor alpha,TNF- α)含量 ;并记录新生儿体重及妊娠结局。 结果 轻、中、重度妊高征组母血清中 s ICAM- 1的含量 [(36 8.5 6± 6 2 .81) μg/L、(6 0 6 .6 3± 10 5 .0 4 ) μg/ L、(85 9.36± 2 0 0 .92 ) μg/ L]均显著高于对照组 [(2 36 .6 9± 96 .33) μg/ L](P<0 .0 5 ,P<0 .0 1,P<0 .0 1) ,中、重度妊高征组母血清中 IL- 1β及 TNF- α的含量均显著高于对照组(P<0 .0 5 ,P<0 .0 1) ;中、重度妊高征组 s ICAM- 1的水平与相应 IL- 1β及 TNF- α的水平呈显著的正相关 (r=0 .6 97,P<0 .0 1;r=0 .74 6 ,P<0 .0 1)。重度妊高征组伴胎儿生长受限 (fetal growth restric-tion,FGR)者血中 s ICAM- 1含量显著高于同组其他孕妇之含量 (P<0 .0 5 )。妊高征组  相似文献   

9.
目的 探讨孕妇血浆血管性假血友病因子(vWF)及内皮素(ET-1)水平变化与妊娠高血压综合征(妊高征)发病的关系。方法 应用酶联免疫吸附试验和放射免疫分析法,分别测定36例妊高征患者(妊高征组)及18例正常妊娠妇女(正常妊娠组)血浆中vWF及ET-1水平,并以19例健康未孕妇女(正常未孕组)为对照。结果 正常妊娠组vWF为(131.6±39.2)%,轻度妊高征患者血浆vWF为(135.9±30.9)%,二者比较,差异无显著性(P>0.05);正常妊娠组ET-1为(47.1±4.7)pg/L,轻度妊高征患者为(63.7±4.8)pg/L,二者比较,差异有极显著性(P<0.01)。中、重度妊高征患者血浆vWF为(174.4±35.4)%,ET-1为(92.6±19.1)pg/L,与正常妊娠组比较,差异均有极显著性(P<0.01)。妊高征患者血浆vWF与ET-1呈明显正相关。结论 vWF和ET-1可作为判断妊高征病情程度的指标;vWF和ET-1在妊高征发病中起相互协同作用。  相似文献   

10.
肿瘤坏死因子对妊高征的致病作用及与内皮素的关系   总被引:2,自引:0,他引:2  
目的:探讨肿瘤坏死因子在妊高征发病中的作用及与内皮素的关系。方法:采用放射免疫法测定了46例妊高征患者(妊高征组)和20例正常晚期妊娠妇女(对照组)血浆肿瘤坏死因子(TNF)和内皮素(ET-1)的质量浓度。结果,妊高征组中,重度患者TNF和ET-1质量浓度明显高于对照且和轻度患者(P〈0.05及P〈0.01);产后72小时两者质量浓度均明显下降。对照组血浆TNF与ET-1质量浓度无相关性,而妊高征  相似文献   

11.

Purpose

Researchers have hypothesized that an imbalance of immune cells in the uterine decidua and a dysfunction in cytokines they produce may contribute to recurrent pregnancy loss (RPL). The objective of this study was to determine if IL-22, IL-23 and IL-17 are expressed abnormally in the decidua of patients with RPL compared to those women with a normal pregnancy. We also sought to confirm that uterine natural killer (uNK) cells are lower in the decidua of patients with RPL, as well as identify IL-22 expression by uNK cells.

Methods

After meeting strict inclusion criteria, maternal decidua of nine patients with unexplained RPL and a confirmed euploid fetal loss, and 11 gestational age-matched patients undergoing elective pregnancy termination were included in our analysis. Quantitative real time-polymerase chain reaction (qRT-PCR) was performed to quantify RNA expression, Western blot was performed to quantify protein expression and immunohistochemistry (IHC) was performed to identify IL-22 and uNK cells.

Results

We found that women with unexplained RPL and a euploid fetal loss had significantly less gene and protein expression of IL-22 in the decidua. Additionally, we found that IL-22 is primarily expressed by uNK cells in the decidua.

Conclusions

In conclusion, our results suggest that lower levels of IL-22 in the uterine decidua in patients with unexplained RPL may contribute to a disruption of decidual homeostasis and ultimately lead to early pregnancy loss.  相似文献   

12.
目的:检测子宫内膜异位症(endometriosis,EMS)患者腹腔液中IL-6、IL-8、IL-10含量及其临床意义。方法:剖腹探查手术中采集EMS组及对照组的腹腔液,用酶联免疫吸附法(ELISA)测细胞因子水平。EMS组中,13份测IL-6,16份测IL-8,22份测IL-10,共51份,对照组检测57份。结果:EMS组和对照组IL-6的含量分别为155.88±114.92ng/L和28.74±25.88ng/L(P<0.01)。IL-8的含量分别为630.97±404.72ng/L和63.05±62.3ng/L(P<0.01)。IL-10也明显高于对照组[(38.88±38.75ng/L比10.45±4.33ng/L(P<0.01)〕。结论:EMS患者腹腔液中IL-6、IL-8及IL-10均升高,提示EMS患者的巨噬细胞活性增强,细胞因子含量增加,可干扰患者免疫调节功能。  相似文献   

13.
A successful pregnancy has been postulated to be the result of a discrete balance between T-helper 1 (Th1) and T-helper 2 (Th2) type cytokines involved in growth and development of the conceptus. The aim of the present study was to examine the effect of Th1 cytokines (interleukin- 1β (IL- 1β) and tumor necrosis factor-alpha (TNFα)) on the release of Th2 cytokines including IL-6 and IL-10 by trophoblast cells obtained from term placenta. Trophoblast cells isolated by enzymatic disaggregation and Percoll gradient fractionation were cultured in supplemented medium alone or with varying concentrations of the selected recombinant cytokines. After 48 h of incubation, samples of the culture supernatant were analyzed for the Th2 cytokines IL-6 and IL-10 using specific ELISA assays. Both IL-1β and TNFα had no effect on the cell number and viability as determined by MTT assay. IL-1β significantly stimulated trophoblast release of IL-6 in a dose-dependent manner (3.3-, 5.5-, 10.3- and 22 4-fold higher compared to the control at 10, 50, 100, 500 U IL-1β/ml respectively, p < 0.05). TNFα also stimulated release of IL-6 by these cells. However, the stimulation at lower concentrations was not very high and a significant (p < 0.05) stimulation was observed only at higher concentrations (1.1-, 1.3-, 2.6- and 5.9-fold higher at 500, 1000, 1500, 2000 U TNFα/ml respectively). In contrast, neither IL-1β or TNFα exerted any significant effect on IL-10 release by term trophoblast cells (p > 0.05). The results of this study provide evidence that production of Th2 cytokines might be under the control of different regulatory pathways.  相似文献   

14.
ObjectivesThe possible mechanism of preeclampsia is investigated in this study to facilitate the exploration of the future remediation of this disease by analysing the changes of IL-17 and IL-35 in peripheral blood and placental tissue of pregnant women with preeclampsia (PE).Materials and methodsThe study was conducted using 45 healthy pregnant women as the control group and 90 pregnant women in the preeclampsia group, including 45 cases with severe preeclampsia and 45 cases with mild preeclampsia. All of 135 pregnant women underwent caesarean delivery. IL-17 and IL-35 concentrations in the serum were measured by ELISA, and IL-17 and IL-35 expression in placental specimens was detected by immunohistochemistry.ResultsThere were no statistically significant differences in age among the three study groups. Serum IL-17 levels were significantly higher in PE patients than in healthy pregnant women (P < 0.01). The ratio of positive staining for IL-17 was markedly higher in mild PE tissues (84.44%; 38/45) and severe PE tissues (86.67%; 39/45) than in healthy pregnant tissues (35.56%; 16/45) (P < 0.01). The strong positive rates for IL-17 were markedly higher in mild PE tissues (48.89%; 22/45) and severe PE tissues (68.89%; 31/45) than in healthy pregnant tissues (13.33%; 6/45) (P < 0.01). No differences between mild PE tissues and severe PE tissues were noted in both positive case rates and strong positive rates. Consistent with this finding, the ratio of strong positive staining for IL-35 was higher in healthy pregnant tissues (66.67%; 30/45) than in mild PE tissues (33.11%; 14/45) and severe PE tissues (26.67%; 12/45) (P < 0.01).ConclusionsThe abnormal increase in serum and placental of IL-17 has an association with the formation and development of PE. IL-35 expression is significantly lower in severe PE placenta tissue and serum compared with normal pregnant women. These results suggested that IL-17/IL-35 imbalance may play a role in the pathophysiology of PE.  相似文献   

15.
【摘 要】 目的:检测子宫腺肌病在位/异位内膜Toll样受体(Toll-like receptors,TLRs)表达,探讨TLRs表达与组织炎症病理的相关性。方法:标本选自同济大学附属杨浦医院收治的子宫腺肌病手术患者24例,分别取在位内膜(eutopic endometrium,EU)、异位内膜(ectopic endometrium,EC),并以正常子宫内膜(control endometrium,CE)为对照。检测CE、EU、EC组中TLRs mRNA及蛋白表达,同时检测白细胞介素(IL)-6、IL-8 mRNA表达。结果:逆转录聚合酶链反应(RT-PCR)检测显示:IL-6、IL-8 mRNA在EC、EU组中表达均高于CE组(P<0.01),且EC组高于EU组(P<0.01)。TLR1~6、8、9 mRNA在EC、EU组中表达高于CE组(P<0.05),除外TLR2,其余TLRs在EC组中表达高于EU组(P<0.01)。TLR7 mRNA在EU组中表达高于CE组(P<0.05),而EC组与CE组、EU组与EC组之间差异无统计学意义。蛋白质印迹(Western blot)检测显示:TLR1、4~6、8、9在EC、EU组中表达高于CE组(P<0.01),且EC组高于EU组(P<0.01)。TLR2在EC组中表达高于CE组(P<0.05),而EU组与CE组、EU组与EC组之间差异无统计学意义。TLR3、7在EC组中表达高于EU组及CE组(P<0.05),而EU组与CE组之间差异无统计学意义。Pearson相关性分析显示,子宫腺肌病EU、EC组TLRs mRNA与IL-6、IL-8均呈正相关;其中TLR2、4、5、9与IL-6、IL-8均呈正相关(P<0.05)。结论:子宫腺肌病病灶处于炎症病理状态,腺肌病EU、EC组TLRs整体呈高表达,并与IL-6、IL-8具有良好的相关性,提示TLRs信号介导免疫炎性体系可能涉及子宫腺肌病炎症病理形成及发展。  相似文献   

16.
OBJECTIVE: We investigated the role of interleukin (IL)-6 and IL-1 receptor antagonist (IL-1ra) in pre-term premature rupture of the membranes (PROM). METHOD: Amniotic fluid samples were collected from 10 patients with pre-term PROM (group 1a), 13 patients undergoing genetic amniocentesis (group 2), seven patients with normal vaginal delivery (group 3a), and 11 patients with elective cesarean section (group 4a). Umbilical venous blood was collected from nine cases of pre-term PROM (group 1b), 19 cases of normal delivery (group 3b) and nine cases of elective cesarean section (group 4b). RESULTS: The concentration of IL-6 in the amniotic fluid in group 1a was significantly higher than in group 2 (P<0.001), and that in group 3a was significantly higher than in group 4a (P<0.001). The concentration of IL-1ra in amniotic fluid in group 1a was significantly higher than in group 2 (P<0.001). The concentrations of IL-6 in umbilical venous blood were not significant among the groups. The concentration of IL-1ra in umbilical venous blood in group 1b was significantly higher than in group 3b (P<0.05) and group 4b (P<0.05). CONCLUSIONS: High concentrations of amniotic fluid IL-6 present in pre-term PROM, are indicative of intrauterine inflammation, probably due to sub-clinical infection. The high concentrations of IL-1ra in amniotic fluid and umbilical venous blood suggest the possibility that the presence of this anti-inflammatory cytokine serves to prevent the development of overt inflammation.  相似文献   

17.
新生儿缺氧缺血性脑病血浆Th2 源细胞因子水平的研究   总被引:3,自引:0,他引:3  
目的 研究新生儿缺氧缺血性脑病 (HIE)患儿辅助性T淋巴细胞亚群 2 (Th2 )细胞功能变化及其与HIE间的关系。 方法 采用ELISA法和单克隆抗体间接免疫荧光法 ,检测 4 6例HIE患儿不同病期血浆和外周血单个核细胞 (PBMC)体外分别产生白细胞介素 (IL) 6、IL 8、IL 10水平和T细胞IL 2受体 (IL 2R)表达率 ,并与正常足月新生儿脐血 (2 0例 )进行对照。 结果 HIE病程第 1天血浆及PBMC体外产生IL 6 [分别为 6 6 .3、80 4 .5ng L(中位数 ,以下同 ) ]、IL 8(4 10 .5、1983.6ng L)和IL 10 (2 7.9、14 0 .1ng L) ,明显高于正常脐血对照组 (分别为 1.9、187.7;91.0、76 6 .8;2 .6、16 .4ng L) (Z =4 .6 5 3~ 5 .85 6 ,P <0 .0 1) ;中重度组及并发多器官功能损害 (MOD)的HIE患儿血浆及PBMC体外产生IL 6 (分别为 86 .0、12 36 .4 ;111.3、174 6 .9ng L)、IL 8(分别为5 79.5、2 812 .2 ;5 32 .8、2 94 3.3ng L) ,分别高于轻度组 (分别为 5 2 .6、5 83.4 ;335 .3、15 2 8.9ng L)及无MOD组 (分别为 5 6 .6、713.8;35 2 .4、15 72 .4ng L)患儿 (Z =2 .2 2 8~ 2 .70 1,P <0 .0 5 ;Z =2 .877~4 .187,P <0 .0 1) ,而IL 10差异无显著性 (Z =0 .4 5 0~ 1.85 0 ,P >0 .0 5 ) ;T细胞IL 2R表达率 [(5 2 .8± 13.4 ) % ]明显  相似文献   

18.
白细胞介素-8和白细胞介素-6对分娩发动的影响   总被引:16,自引:0,他引:16  
目的 探讨白细胞介素-8(IL-8)、白细胞介素-6(IL-6)在分娩发动中的作用。方法 随机选择孕38 ̄41的54例胎膜完整的单胎初产妇临产前后共60份血清样本,进行IL-8、IL-6水平测定并分进行对比分析。结果 妊娠晚期,随着孕周的增加,血清IL-8水平逐渐增高,逐渐变软展平。IL-8水平与宫颈Bishop评分呈直线正相关。临瓣一血清IL0-8水平明显低于临产水平,且在第一产程各阶段差异显著  相似文献   

19.
子宫内膜异位症患者辅助性T细胞亚群免疫状态的研究   总被引:8,自引:0,他引:8  
目的 探讨辅助性T细胞 (Th)亚群在子宫内膜异位症 (内异症 )发病中的作用。方法 采用酶联免疫吸附法检测 30例内异症患者 (内异症组 )及 2 0例非内异症患者 (对照 1组 )血清及腹腔液中白细胞介素 (IL) 2、6的水平 ;用免疫组化技术分别检测IL 2、IL 6在内异症组患者异位内膜组织和 10例子宫肌瘤患者 (对照 2组 )的正常子宫内膜组织中的表达。结果 内异症组患者血清及腹腔液中位数IL 6水平分别为 5 3、2 1ng/L ,对照 1组患者血清及腹腔液中位数IL 6水平分别为 2 5、0 9ng/L ,两组妇女血清和腹腔液中IL 6水平分别比较 ,差异均有统计学意义 (P <0 0 5 ) ;内异症组Ⅲ~Ⅳ期患者血清及腹腔液中位数IL 6水平分别为 13 6、4 1ng/L ,Ⅰ~Ⅱ期患者血清及腹腔液中位数IL 6水平分别为 3 7、1 6ng/L ,Ⅲ~Ⅳ期患者与Ⅰ~Ⅱ期患者血清及腹腔液中位数IL 6水平比较 ,差异均有统计学意义 (P <0 0 5 ) ;内异症组IL 2 /IL 6比值在血清及腹腔液中分别为 0 7、1 1,均分别低于对照组的 0 8、6 2 ,差异也有统计学意义 (P <0 0 5 )。内异症组患者腹腔液与血清IL 6水平呈正相关 (r =0 74 5 ,P <0 0 1) ,血清及腹腔液中IL 6水平与IL 2 /IL 6比值均呈负相关 (r =- 0 4 0 6 ,P <0 0 5 ;r =- 0 4 80 ,P <0 0 5 )  相似文献   

20.
IL-4和IL-12在宫颈癌的表达及临床意义   总被引:1,自引:0,他引:1  
目的:探讨白细胞介素-4(IL-4)和白细胞介素-12(IL-12)在宫颈癌的表达及临床意义。方法:应用免疫组化PV6000通用二步法,检测IL-4和IL-12在20例正常宫颈上皮组织和72例宫颈癌组织蜡块中的表达,分析其与宫颈癌临床病理参数之间的关系。结果:IL-4在正常对照组和宫颈癌组的阳性表达率分别是20%和63.9%,两者差异有统计学意义(P<0.01);IL-12在两组的阳性表达率分别是55%和48.6%,两者差异无统计学意义(P>0.05)。IL-4在宫颈癌的表达与FIGO分期及有无淋巴结转移有关(P<0.05),IL-12表达与宫颈癌分化程度及淋巴结转移有关(P<0.05)。结论:IL-4高表达和IL-12低表达可能参与了宫颈肿瘤细胞的免疫逃逸机制,其程度高低提示肿瘤生长速度及浸润程度。  相似文献   

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