C/C复合材料表面等离子喷涂HA涂层在SBF中的试验

目的 探讨不同模拟体液对HA涂层体外生物学行为的影响。方法采用等离子体喷涂法,在碳／碳复合材料表面制备HA涂层,并对涂层进行了热处理。利用X射线衍射仪(X-ray diffraction)、扫描电子显微镜(Scanning electron microscopy)等检测手段,分析该涂层的物相和形貌,观察HA涂层在模拟体液中的影响。结果XRD检测结果表明,在模拟体液浸泡过程中,涂层的主要组成相的相对含量和结晶度不断发生变化。由SEM分析结果可知,在浸泡过程中,内送粉方式下制得的HA涂层的表面沉积物呈现近似网状的结构。同时,在Ringer溶液中,可以观察到HA涂层溶解痕迹。结论通过适当的热处理可以恢复HA的结构完整性,同时提高涂层的结晶度。     

树突状细胞负载肝癌抗原肽疫苗体外诱导特异性免疫学反应的研究

目的：研究树突状细胞(dendritic cell，DC)负载肝癌抗原肽EPVTKAEML体外诱导特异性CTL的能力及其抑癌效果。方法：用顺序特异引物聚合酶链反应技术(PCR—SSP)选择HLA—B7表型供者，从脾组织中分离、培养DC-EPVTKAEML特异性CTL。用^51Cr释放法检测CTL的杀伤活性，并用抗HLA-1分子单抗(mAb)进行杀伤抑制实验。结果：找到4例HLA-B7杂合子供者，用DC负载HLA-B7限制的抗原肽EPVTKAEML可诱导特异性CTL反应，对肝癌细胞HHCC有较强的杀伤作用。结论：DC负载抗原肽EPVTKAEML在体外可诱发较强的特异性免疫反应。     

高效凝胶色谱一步法制备级纯化单克隆抗体

作者采用ＰｈａｒｍａｃｉａＳｅｐｈａｃｒｙｌＳ—３００凝胶色谱柱，建立了ＩｇＧ类ＭｃＡｂ的一步法制各级纯化方法。该法是将ＭｃＡｂ腹水直接上样，用ｐＨ７．４１０ｍｍｏｌ／ＬＰＢＳ洗脱（流速０．５ｍｌ／ｍｉｎ），即得到纯化的ＭｃＡｂ。一次上样量４０～５０ｍｌ腹水，回收率为８５％－９０％．整个纯化周期４ｈ。纯化的ＭｃＡｂ经ＳＤＳ—ＰＡＧＥ测定，纯度＞９０％，免疫组化ＡＢＣ法测定活性为１：８００００（７．８×１０－１１ｍｏｌ／Ｌ）。该法操作简单、快速，只要有一台核酸／蛋白检测仪，便可进行制备级水平的纯化。     

结肠的器官内淋巴管

本文对家兔、大白鼠和豚鼠的结肠器官内淋巴管进行了光镜和电镜观察。结肠粘膜层毛细淋巴管位于肠腺底与粘膜肌之间。粘膜下层毛细淋巴管位于粘膜肌直下方;淋巴管多位子其深方。肌层和浆膜层存有毛细淋巴管和淋巴管。毛细淋巴管内皮细胞质中有大量的囊泡,囊泡与细胞质膜有密切关系,淋巴管内皮细胞间的连接主要有三种形式,即重叠连接、指状插入连接和端端连接。淋巴管壁存有内皮内管道。     

肝癌特异性超抗原SEA(D227A)基因表达载体的构建与表达

目的：构建受AFP顺式作用元件调控的超抗原表达载体，将SEA(D227A)特异性的表达于AFP阳性肝癌细胞膜表面。方法：PCR扩增AFP基因启动子、增强子、linker—CD80tm和SEA(D227A)。将上述片断插入逆转录病毒载体pLXSN的多克隆位点，构建AFP基因顺式作用元件调控的肝癌特异性减毒超抗原表达载体(pLXSN SEA(D227A)—linker—CD80tm)。通过脂质体介导，以表达载体转染表达或不表达AFP的肿瘤细胞系，用RT—PCR和间接免疫荧光染色，检测SEA的表达。结果：成功地将AFP基因的启动子、增强子、linker—CD80tm和SEA(D227A)克隆到逆转录病毒载体pLXSN的多克隆位点，酶切鉴定和DNA序列分析无误，RT—PCR和间接免疫荧光法检测证实，SEA(D227A)能在AFP阳性的肝癌细胞膜特异性表达。结论：AFP顺式作用元件修饰的超抗原表达载体的构建，为下一步用其强化肝癌的免疫治疗奠定了基础。     

原发性开角型青光眼与高血压的关系

目的 探讨原发性开角型青光眼与高血压病的关系．方法 随机选择确诊原发性开角型青光眼50例，高血压病50例，观察眼压、血压、视乳头C／D比，视野，归纳总结．结果 50例原发性开角型青光眼中，血压高者25例(50％)．50例高血压病中，眼压高者38例(76％)，视野损害40例(80％)，光敏度下降35例(70％)，中心暗点25例(50％)，周边视野缩小17例(34％)，生理盲点扩大17例(34％)．结论 原发性开角型青光眼与高血压病有极大关联．     

施万细胞对大鼠脊髓半横切后背核神经元存活及其表达NOS的影响

目的：探讨移植的施万细胞对大鼠脊髓半横切后背核神经元存活及其表达NOS的影响。方法：50只成年SD大鼠被分为实验组和对照组。在胸11脊髓段半横切后立即在损伤处移植入施万细胞。结果：脊髓半横切后，15d和25d对照组L1脊髓段损伤侧背核神经元的存活数均比未损伤侧的明显减少。存活的神经元胞体出现明显皱缩，有些神经元呈现NADPH－d阳性。15d和25d施万细胞组L1脊髓段损伤侧背核神经元的存活数则比同期对照组的明显增加，表达NOS的存活神经元数也随之增多。但存活的神经元胞体仍然是皱缩的。结论：移植的SCs可促进受损伤的背核神经元存活及其表达NOS，但不能阻止其胞体出现皱缩。     

Custom step wedge blocking using dynamic multileaf collimation for parametrial pelvic boost irradiation following brachytherapy for carcinoma of the cervix

Carcinoma of the cervix is typically treated with a combination of intracavitary brachytherapy and external beam radiation. The external beam dose is delivered with whole pelvis fields followed by split fields that protect midline organs at risk (bladder and rectum) while treating the parametria. Three approaches have been developed to shield midline structures: a simple rectangular block, a block customized to a single brachytherapy isodose line, and a step wedge filter constructed to conform to multiple brachytherapy isodose lines. A customized step wedge filter has the potential to produce a more homogeneous dose distribution but has not achieved widespread use due to labor intensive construction. We have developed a simple, novel method to produce a custom midline step wedge using dynamic multileaf collimation (dMLC). A comparison of film measurements in a phantom with the dose calculated by a commercial treatment planning system demonstrated agreement within 3% or 3 mm. The technique requires delivery times comparable to conventional techniques.     

Validation of target volume and position in respiratory gated CT planning and treatment

The capability of a commercial respiratory gating system based on video tracking of reflective markers to reduce motion-induced CT planning and treatment errors was evaluated. Spherical plastic shells (2.8-82 cm3), simulating the gross target volume (GTV), were placed in a water-filled body phantom that was moved sinusoidally along the longitudinal axis of the CT scanner and the accelerator for +/- 1 cm at 15-30 cycle/min. During gated CT imaging, the x-ray exposure was initiated by the gating system shortly before the end of expiration (so that the imaging time would be centered at the end of expiration); it was terminated by the scanner after completion of each slice. In nongated CT images, the target appeared distorted and often broken up. GTVs volume errors ranged 16%-110% in axial scans, and 7%-36% in spiral scans. In gated CT images, the spheres appeared 3 and 5 mm longer than their actual diameters (volume errors 2%-16%), at the respective respiration rates of 15 and 20 cycles/min. At 30 cycles/min the target appeared 1 cm longer, and volume error ranged 25%-53%. During treatment, gating kept the beam on for a duration equal to the CT acquisition time of 1 s/slice. The difference in positional errors between gated CT and portal films was 1 mm, regardless the size of residual motion errors. Because of the potential of suboptimal placement of the gating window between CT imaging and treatment, an extra 1.5-2.5 mm safety margin can be added regardless of the size of residual motion error. For respiratory rates > or = 30 cycles/min, the effectiveness of gating is limited by large residual motion in the 1 s CT acquisition time.