中华实用儿科临床杂志
中華實用兒科臨床雜誌
중화실용인과림상잡지
Journal of Applied Clinical Pediatrics
2014年
5期
338-341
,共4页
王娟%郭桂梅%夏敏%郑林%郝胜%黄文彦%何威逊
王娟%郭桂梅%夏敏%鄭林%郝勝%黃文彥%何威遜
왕연%곽계매%하민%정림%학성%황문언%하위손
过敏性紫癜%浆细胞样树突状细胞%趋化因子
過敏性紫癜%漿細胞樣樹突狀細胞%趨化因子
과민성자전%장세포양수돌상세포%추화인자
Henoch-Sch(o)nlein purpura%Plasmacytoid dendritic cells%Chemokines
目的 研究浆细胞样树突状细胞(pDC)在过敏性紫癜(HSP)患儿外周血和肾脏组织中的表达和分布情况,探讨pDC在紫癜性肾炎发病中的作用.方法 40例HSP患儿,其中急性期28例,缓解期12例,分离患儿外周血单个核细胞,流式细胞术检测pDC的表达;设立正常对照组(15例).同时抽提外周血总RNA并反转录为cDNA,以实时荧光定量PCR法检测患者组和正常对照组趋化因子干扰素γ诱导蛋白10 (CXCL10)、CC类趋化因子配体5(CCL5)及相应受体CXC亚家族趋化因子受体3(CXCR3)、趋化因子受体5(CCR5)mRNA的定量表达水平(以2-△△Ct值表示).应用免疫组织化学技术,观察8例行肾活检患者肾脏组织中pDC的分布;设立正常对照(3例).结果 HSP急性期患者外周血pDC表达的百分数为0.051±0.039,低于缓解期的0.181 ±0.082和正常对照组的0.166±0.079(P<0.000 1).HSP患者外周血高表达CXCL10、CCL5,而低表达CXCR3、CCR5.正常对照肾脏组织未见pDC浸润,而紫癜性肾炎患者pDC呈局灶节段分布于肾小球系膜区.结论 pDC在HSP患儿中表达异常,紫癜性肾炎的发生可能与外周血中pDCs在趋化因子作用下向肾组织的迁移,引起局部炎性反应有关.
目的 研究漿細胞樣樹突狀細胞(pDC)在過敏性紫癜(HSP)患兒外週血和腎髒組織中的錶達和分佈情況,探討pDC在紫癜性腎炎髮病中的作用.方法 40例HSP患兒,其中急性期28例,緩解期12例,分離患兒外週血單箇覈細胞,流式細胞術檢測pDC的錶達;設立正常對照組(15例).同時抽提外週血總RNA併反轉錄為cDNA,以實時熒光定量PCR法檢測患者組和正常對照組趨化因子榦擾素γ誘導蛋白10 (CXCL10)、CC類趨化因子配體5(CCL5)及相應受體CXC亞傢族趨化因子受體3(CXCR3)、趨化因子受體5(CCR5)mRNA的定量錶達水平(以2-△△Ct值錶示).應用免疫組織化學技術,觀察8例行腎活檢患者腎髒組織中pDC的分佈;設立正常對照(3例).結果 HSP急性期患者外週血pDC錶達的百分數為0.051±0.039,低于緩解期的0.181 ±0.082和正常對照組的0.166±0.079(P<0.000 1).HSP患者外週血高錶達CXCL10、CCL5,而低錶達CXCR3、CCR5.正常對照腎髒組織未見pDC浸潤,而紫癜性腎炎患者pDC呈跼竈節段分佈于腎小毬繫膜區.結論 pDC在HSP患兒中錶達異常,紫癜性腎炎的髮生可能與外週血中pDCs在趨化因子作用下嚮腎組織的遷移,引起跼部炎性反應有關.
목적 연구장세포양수돌상세포(pDC)재과민성자전(HSP)환인외주혈화신장조직중적표체화분포정황,탐토pDC재자전성신염발병중적작용.방법 40례HSP환인,기중급성기28례,완해기12례,분리환인외주혈단개핵세포,류식세포술검측pDC적표체;설립정상대조조(15례).동시추제외주혈총RNA병반전록위cDNA,이실시형광정량PCR법검측환자조화정상대조조추화인자간우소γ유도단백10 (CXCL10)、CC류추화인자배체5(CCL5)급상응수체CXC아가족추화인자수체3(CXCR3)、추화인자수체5(CCR5)mRNA적정량표체수평(이2-△△Ct치표시).응용면역조직화학기술,관찰8례행신활검환자신장조직중pDC적분포;설립정상대조(3례).결과 HSP급성기환자외주혈pDC표체적백분수위0.051±0.039,저우완해기적0.181 ±0.082화정상대조조적0.166±0.079(P<0.000 1).HSP환자외주혈고표체CXCL10、CCL5,이저표체CXCR3、CCR5.정상대조신장조직미견pDC침윤,이자전성신염환자pDC정국조절단분포우신소구계막구.결론 pDC재HSP환인중표체이상,자전성신염적발생가능여외주혈중pDCs재추화인자작용하향신조직적천이,인기국부염성반응유관.
Objective To investigate the expression and distribution of plasmacytoid dendritic cells(pDC) in peripheral blood and renal tissues in children with Henoch-SchSnlein purpura(HSP),and explore the role of pDCs in the pathogenesis of Henoch-Schtnlein purpura nephritis(HSPN).Methods Among the 40 children with HSP,28 cases were in the active phase(renal biopsy performed in 8 cases of them) and the other 12 in remission phase.Peripheral blood mononuclear cells were isolated,and the expression of pDC was detected by flow cytometry.The normal control group was established (n =15).Total RNA of peripheral blood was extracted and transcripted into cDNA.Sybr green dye based real-time quantitative PCR method was used to compare the expression(indicated as 2-△Ct value) of CXC motif chemokine 10 (CXCL10),CC chemokine ligand 5 (CCL5),chemokine CXC subfamily receptor 3 (CXCR3),CC chemokine receptor 5 (CCR5) in children with HSP and those in the controls.Immunohistochemistry labeling technique was used to detect the distribution of pDC in renal tissues from renal biopsy,and the normal controls were established (n =3).Results The expression percentage of pDC in peripheral blood in active phase was 0.051 ± 0.039,significantly lower than those in remission phase (0.181 ± 0.082) and the normal controls (0.166 ± 0.079) (P < 0.000 1).Chemokines genes CXCL10 and CCL5 were overexpressed in peripheral blood ceils of acute phase HSP children,but chemokine receptors CXCR3,CCR5 were lowly expressed compared with normal controls.There was almost no expression of pDC in the normal control renal tissues,while pDC was infiltrated in glomeruli of HSPN children.Conclusions The number of pDC and chemokines' expression in peripheral blood is abnormal,and the pathogenesis of nephritis may be involved with the pDC in peripheral blood to migrate to the renal tissues.