供者特异性抗原静脉输注联合抗γ链单克隆抗体诱导小鼠皮肤移植物免疫耐受

目的　探讨静脉输注供者特异性抗原联合抗白细胞介素2受体(IL 2R)γ链单克隆抗体诱导移植免疫耐受的可行性。方法　在C57BL/6小鼠建立H Y皮肤移植模型,术前7 d给予5×106个供者脾细胞静脉输注,并分别于术前6 d和4 d给予抗白细胞介素2受体γ链单克隆抗体(4G3、3E12及TUGm2各0.5 mg)和抗IL 2Rβ单克隆抗体(TM β1,0.5 mg)混合液2.0 mg腹腔注射,以单纯行H Y皮肤移植模型和静脉输注供者特异性抗原的H Y皮肤移植模型为对照,观察皮肤移植物的存活时间。结果　联合给予抗白细胞介素2受体γ链单克隆抗体和供者特异性抗原输注组的皮肤移植物存活时间均超过100 d,显著长于单纯H Y皮肤移植组的33.42 d(P<0.01)及仅输注供者特异性抗原H Y皮肤移植组的14.71 d(P<0.01)。结论　在H Y皮肤移植模型中,静脉输注供者特异性抗原联合抗白细胞介素2受体γ链单克隆抗体可以成功地诱导受者对皮肤移植物的免疫耐受。     

乳腺病变X线立体定位钢丝置入移位的分析

目的分析乳腺立体定位下钢丝置入移位的表现、原因、处理方法，提高术前定位的准确性。方法行立体定位置入钢丝患者79例，96个病变，发生钢丝移位13例。结果立体定位中发生钢丝移位5例，原因分别来自于患者和操作医师；立体定位完成后钢丝移位5例，原因是局麻注射药物过多，导致乳腺Z轴的深度与计算机提示的实际深度不符合、放置定位针的方法不正确、拔出钢丝外套针套时疏忽钢丝是否已锚定病变。处理方法：可按照钢丝提示位置向病变方向移位2cm以内进行手术，重新放置第2根钢丝，将双J型钢丝收入针套并取出体外，重新定位。手术中钢丝脱出2例，因术后过分提拉钢丝所致，放射科医师放置钢丝后应向外科医师准确描述深度、方向，并从距离钢丝头端距离皮肤最近处取切口手术。术后标本未见钙化1例，与钙化位于手术电刀破坏的腺体内有关，可扩大范围切除并短期复查，证实钙化是否完整切除。结论正确认识乳腺X线立体定位下钢丝移位的表现，熟练掌握其处理方法，可提高对不可触及的乳腺病变的定位准确性，正确引导外科手术。     

注射自体成纤维细胞除皱的临床应用

目的观察体外培养的自体成纤维细胞注射的面部除皱临床效果,探讨其在面部年轻化治疗中的意义。方法取10例睑袋及上睑松弛手术切除的皮肤行体外培养,细胞数量扩增至108后注射入面部不同治疗部位皮肤的真皮深层,共注射3次,每次间隔2周。结果10例随访6~12月,各例皱纹均得到明显改善,未出现免疫排斥、肉芽肿等并发症。结论应用培养的自体成纤维细胞注射去除面部浅表皱纹,治疗过程简便、创伤微小、安全、效果确实,是一种较好地填充除皱方法。由于尚缺乏更长期的随访结果,远期疗效还有待进一步观察。     

TARP钢板系统在难复型寰枢椎脱位手术中的临床应用

目的探讨经口咽前路寰枢椎复位钢板系统（TARP）在难复型寰枢椎脱位的临床应用。方法自2003年4月-2004年9月，对13例陈旧性的难复型寰枢椎脱位患者行经口咽前路松解减压，应用TARP系统复位和固定，两侧寰枢关节间植入自体髂骨融合。结果除1例因跌倒引起螺钉松动再次脱位外，均固定牢固，融合理想，脊髓减压满意。结论经口咽前路寰枢椎复位钢板系统一次完成寰枢椎脱位的复位和固定是治疗陈旧性难复型寰枢椎脱位较为理想的手术方法。     

家族性特发性基底节钙化

家族性特发性基底节钙化（familial idiopathic basal ganglia calcification，FIBGC）是一种以影像学上有基底节及脑其他部位钙化为特征的神经系统变性疾病。大多数患在童年及青少年时期是健康的，而到了30-50岁时，典型患会逐渐出现神经精神以及运动障碍。首发症状通常包括动作笨拙、易疲劳、步态不稳、言语缓慢、吞咽困难、不自主运动、肌肉痉挛等，经常会有各种类型的癫痫发作。神经精神症状往往是首发或最突出的表现，轻仅仅为轻度注意力或记忆力的下降，重则会出现人格及行为改变，终致精神病或痴呆。[第一段]     

3种肠道清洁方法效果比较

目的 探讨顺产儿脐部护理中修剪法配合Orem自理模式的应用效果。方法 将100名顺产新生儿随机分为对照组和观察组各50名。对照组按常规进行脐部护理；观察组择期行脐部修剪，同时根据Orem自理模式进行全补偿、部分补偿及支持一教育护理模式进行护理。观察两组脐带出血、脱落及疑似感染情况。结果 两组均未出现脐带出血情况；两组出生后9d回访时脐带脱落比较，差异有显著性意义（P〈0．05）。结论 修剪法配合Orem自理模式进行脐部护理，能促进新生儿脐带早脱落。     

The application of basic science concepts to clinical problem-solving

This study looks at the relationship between anatomical concepts held by medical students and their clinical application, and develops a testable model of how students use basic science concepts for clinical problem-solving. According to the model, the essential prerequisites to solve a clinical problem using basic science information include the appropriate basic science knowledge, the ability to collect and interpret clinical information, with the key concept being the link that must then be made between clinical data and basic science. A detailed analysis of the individual components of the model should help to clarify and resolve some of the debate about the nature and balance of basic science and clinical education. A neurological diagnostic problem was used to test the assumptions of the model in a group of medical students who had minimal clinical experiences. There was no demonstrable relationship between anatomical knowledge as assessed by conventional tests and the diagnosis. There was a powerful relationship between measures of organization of knowledge and diagnosis, suggesting that the organization and development of concepts is the key to correct diagnosis. The findings have significant implications for assessment purposes and suggest that standard methods as generally practised may not measure the appropriate conceptual development and are not congruent with curricular objectives. Through the examination of its different learning outcome measures, the model may also be used to provide a profile of individual students or classes, which should help teachers and students deal with difficulties that may be experienced in learning to link clinical and basic science concepts.     

Antibodies against dengue virus E protein peptide bind to human plasminogen and inhibit plasmin activity

Both mice and rabbits immunized with dengue virus E protein peptide spanning amino acids 100–119 (D4E) produced antibodies that reacted not only with the D4E peptide itself but also with human plasminogen, as shown by ELISA and Western blot. Sera from dengue virus-hyperimmunized mice and dengue patients also contained antibodies against D4E and plasminogen. Furthermore, such sera all contained plasmin inhibitory activity. Using affinity-purified anti-D4E antibodies and free D4E peptide for competitive inhibition, we demonstrated that the inhibition of plasmin activity was due to anti-D4E antibodies rather than other substances in the sera. Taken together, these results suggest dengue virus E protein amino acids 100–119 are a cross-reactive immunogenic region, and antibodies against this region may interfere with human fibrinolysis.     

Distribution of α-integrin subunits in fetal polycystic kidney diseases

An alteration in cell/matrix interactions is one of the suggested mechanisms leading to cyst formation in polycystic kidney diseases. Most of these interactions are mediated by β1-integrins, a subfamily of integrin receptors, formed by the association of the β1-chain with different α-subunits. To date, no study on α-integrin subunit distribution during the early stages of cyst development has been reported. Using immunofluorescence, we analyzed the distribution of α-integrin subunits (α1, α2, α3, α5, and α6) and basement membrane proteins in kidneys of fetuses with autosomal dominant (ADPKD) or autosomal recessive polycystic kidney disease (ARPKD). The distribution was compared with that observed in normal fetal and post-natal kidneys, and in fetal cystic dysplasia and Meckel syndrome. Marked increase in α1-integrin staining was observed in normal and cystic collecting duct cells of both polycystic diseases (PKD), compared with normal and cystic controls. The distribution of integrin subunits α2, α3, and α6 was irregular in cyst epithelial cells of PKD and cystic controls. The increased expression of the α1-subunit specifically observed in PKD collecting duct cells may be an early consequence of the genetic defect in ARPKD. In ADPKD it parallels the reported expression of polycystin, the protein product of PKD1. The irregular expression of α2, α3, and α6 integrin subunits observed in all types of cysts suggests that cell/matrix interactions are altered early and may participate in the development of cysts, perhaps by contributing to the deregulation of cell survival in cystic diseases. Received May 28, 1996; received in revised form October 2, 1996; accepted October 25, 1996