中华血液学杂志
中華血液學雜誌
중화혈액학잡지
Chinese Journal of Hematology
2014年
12期
1111-1114
,共4页
孙梅%闪丹%顾蔚%孙幸%何斌%裴孝平%陈沛帅%管俊%姜扬文
孫梅%閃丹%顧蔚%孫倖%何斌%裴孝平%陳沛帥%管俊%薑颺文
손매%섬단%고위%손행%하빈%배효평%진패수%관준%강양문
血小板减少%糖皮质激素类%丙种球蛋白%利妥昔单抗%治疗结果
血小闆減少%糖皮質激素類%丙種毬蛋白%利妥昔單抗%治療結果
혈소판감소%당피질격소류%병충구단백%리타석단항%치료결과
Thrombocytopenia%Glucocorticoids%Gamma globulin%Rituximab%Outcome
目的 观察和评价糖皮质激素、利妥昔单抗、静脉丙种球蛋白(IVIG)对原发免疫性血小板减少症(ITP)患者B淋巴细胞抗原表达的影响.方法 71例ITP患者纳入研究,按照治疗方案分为糖皮质激素组(21例)、糖皮质激素联合利妥昔单抗组(31例)及糖皮质激素联合IVIG组(19例),以30名健康志愿者作为对照组.治疗前后测定CD19、CD20、CD80 、CD86抗原表达水平及血小板计数.结果 ①所有患者在治疗后1周内出血症状均明显好转;PLT均高于治疗前(P<0.05),三组之间比较差异无统计学意义(P>0.05);②三组ITP患者治疗前CD19、CD20表达水平均高于正常对照组(P<0.05),组间比较差异无统计学意义(P>0.05),糖皮质激素+利妥昔单抗组治疗后CD19、CD20表达水平均低于治疗前[(0.03±0.02)%对(15.96±7.72)%;(0.04±0.03)%对(15.98±7.64)%;P值均<0.05];③三组ITP患者治疗前CD80、CD86表达水平均高于正常对照组(P<0.05),糖皮质激素组和糖皮质激素+IVIG组治疗后CD80、CD86表达水平与治疗前比较差异无统计学意义(P>0.05),糖皮质激素+利妥昔单抗组治疗后CD80、CD86表达水平低于治疗前[(0.06±0.12)%对(0.74±0.66)%;(0.12±0.19)%对(0.67±0.70)%;P值均<0.05],与其他两组比较差异有统计学意义(P<0.05).结论 糖皮质激素联合利妥昔单抗可靶向清除ITP患者体内B细胞,并下调CD80、CD86表达.
目的 觀察和評價糖皮質激素、利妥昔單抗、靜脈丙種毬蛋白(IVIG)對原髮免疫性血小闆減少癥(ITP)患者B淋巴細胞抗原錶達的影響.方法 71例ITP患者納入研究,按照治療方案分為糖皮質激素組(21例)、糖皮質激素聯閤利妥昔單抗組(31例)及糖皮質激素聯閤IVIG組(19例),以30名健康誌願者作為對照組.治療前後測定CD19、CD20、CD80 、CD86抗原錶達水平及血小闆計數.結果 ①所有患者在治療後1週內齣血癥狀均明顯好轉;PLT均高于治療前(P<0.05),三組之間比較差異無統計學意義(P>0.05);②三組ITP患者治療前CD19、CD20錶達水平均高于正常對照組(P<0.05),組間比較差異無統計學意義(P>0.05),糖皮質激素+利妥昔單抗組治療後CD19、CD20錶達水平均低于治療前[(0.03±0.02)%對(15.96±7.72)%;(0.04±0.03)%對(15.98±7.64)%;P值均<0.05];③三組ITP患者治療前CD80、CD86錶達水平均高于正常對照組(P<0.05),糖皮質激素組和糖皮質激素+IVIG組治療後CD80、CD86錶達水平與治療前比較差異無統計學意義(P>0.05),糖皮質激素+利妥昔單抗組治療後CD80、CD86錶達水平低于治療前[(0.06±0.12)%對(0.74±0.66)%;(0.12±0.19)%對(0.67±0.70)%;P值均<0.05],與其他兩組比較差異有統計學意義(P<0.05).結論 糖皮質激素聯閤利妥昔單抗可靶嚮清除ITP患者體內B細胞,併下調CD80、CD86錶達.
목적 관찰화평개당피질격소、리타석단항、정맥병충구단백(IVIG)대원발면역성혈소판감소증(ITP)환자B림파세포항원표체적영향.방법 71례ITP환자납입연구,안조치료방안분위당피질격소조(21례)、당피질격소연합리타석단항조(31례)급당피질격소연합IVIG조(19례),이30명건강지원자작위대조조.치료전후측정CD19、CD20、CD80 、CD86항원표체수평급혈소판계수.결과 ①소유환자재치료후1주내출혈증상균명현호전;PLT균고우치료전(P<0.05),삼조지간비교차이무통계학의의(P>0.05);②삼조ITP환자치료전CD19、CD20표체수평균고우정상대조조(P<0.05),조간비교차이무통계학의의(P>0.05),당피질격소+리타석단항조치료후CD19、CD20표체수평균저우치료전[(0.03±0.02)%대(15.96±7.72)%;(0.04±0.03)%대(15.98±7.64)%;P치균<0.05];③삼조ITP환자치료전CD80、CD86표체수평균고우정상대조조(P<0.05),당피질격소조화당피질격소+IVIG조치료후CD80、CD86표체수평여치료전비교차이무통계학의의(P>0.05),당피질격소+리타석단항조치료후CD80、CD86표체수평저우치료전[(0.06±0.12)%대(0.74±0.66)%;(0.12±0.19)%대(0.67±0.70)%;P치균<0.05],여기타량조비교차이유통계학의의(P<0.05).결론 당피질격소연합리타석단항가파향청제ITP환자체내B세포,병하조CD80、CD86표체.
Objective To observe the levels of B cell antigen expression treated by glucocorticoid,rituximab or intravenous gamma globulin for immune thrombocytopenia (ITP).Methods 71 patients with ITP were studied,including 21 cases with glucocorticoid (glucocorticoid group),31 with glucocorticoids combined rituximab (rituximab group),and 19 with glucocorticoids combined intravenous gamma globulin (gamma globulin group).30 healthy volunteers were control.Expression levels of CD 19,CD20,CD28,CD80,CD86 and platelet count were detected before and after treatment.Results ① Improvement of bleeding was seen in all cases within one week.The level of platelet count was significantly higher after administration (P < 0.05),but no significant difference among three groups (P > 0.05); ②In the three groups before treatment,the expression of CD19 and CD20 were higher than the control group (P < 0.05).In glucocorticoid group and gamma globulin group,the expression of CD19 and CD20 was almost the same before and after treatment (P > 0.05).But in rituximab group,CD19 [(0.03± 0.02)% vs (15.96±7.72)%,P<0.05] and CD20 [(0.04±0.03)% vs (15.98±7.64)%,P<0.05] were significantly lower after treatment; ③ In the three groups before treatment,the expression of CD80 and CD86 were higher than the control group (P < 0.05).In glucocorticoid group and gamma globulin group,the expression decreased,but no statistical significance (P > 0.05).However,the expression in rituximab group was significantly lower after treatment [CD80:(0.06±0.12)% vs (0.74±0.66)%; CD86:(0.12± 0.19)% vs (0.67±0.70)%; P< 0.05].Conclusion Low dose of rituximab combined glucocorticoid could target on CD20+ B cells and down the expression of CD80 and CD86,thus reversing the immune imbalance in ITP.