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71.
以小鼠心肌组织异位移植和混合淋巴细胞反应为整体和离体模型,观察了阿片受体阻断剂纳曲酮对移植排异反应的影响。结果显示:给动物从术前开始腹腔注射纳曲酮共10天(每日二次,每次5mg/kg)可明显延长移植心肌组织的存活时间;加入纳曲酮(10-4~10-8mol/L)对混合淋巴细胞反应有抑制作用并呈量效关系。同时还观察到,给正常小鼠腹腔注射纳曲酮3天以上,可引起动物脾细胞由ConA诱导的淋巴细胞转化反应受抑制。以上结果说明纳曲酮可抑制移植排异反应,此作用有可能是通过阻断内源性阿片肽所致。 相似文献
72.
目的研究骨髓间充质干细胞(MSC)对脐带血(CB)CD34^+细胞体外增殖和造血重建能力的影响。方法取人骨髓单个核细胞贴壁培养.梭形细胞完全融合后传代,用流式细胞仪检测免疫表型;将CBCD34^+细胞接种到MSC或其他培养液中.比较不同培养条件对造血干细胞扩增能力、集落形成能力及黏附分子表达的影响。结果在加入IL-3的培养体系中.在MSC和细胞因子作用下,CD34^+细胞扩增7d和14d后,有核细胞(NC)、CD34^+细胞和CDl33^+细胞数,实验组均显著多于对照组。CD34+细胞在未加入IL-3的培养体系中培养8d后,实验组NC、CD34^+细胞、CD34^+CD38-细胞和造血祖细胞集落扩增倍数均显著高于对照组。扩增后CD34^+细胞的ALCAM、VLA-α4、VLA-α5、VLA-β1、HCAM、PECAM和LFA-1表达较扩增前无显著变化。结论MSC可为造血干细胞(HSC)体外扩增提供适宜的微环境,有助于CD34^+细胞体外增殖并抑制HSC分化,保持其造血重建潜能和归巢能力。 相似文献
73.
74.
目的作者自1995-2002年采用人造血管移植修复四肢大血管损伤23例,进行回顾性研究人造血管在治疗四肢大血管损伤中的应用。方法23例中男19例,女4例。年龄:21~47岁,平均34.7岁。手术清创和探查后,针对不同的情况选择人造血管移植修复方法。结果采用人造血管移植23例,肢体全部保存,肢体功能恢复较佳。结论四肢大血管损伤救治应快速诊断、快速救治,采用人造血管移植修复四肢主要血管损伤是一种快捷有效的方法。 相似文献
75.
Peer Arts Jessica Garland Alicia B. Byrne Tristan S.E. Hardy Milena Babic Jinghua Feng Paul Wang Thuong Ha Sarah L. King‐Smith Andreas W. Schreiber April Crawford Nick Manton Lynette Moore Christopher P. Barnett Hamish S. Scott 《American journal of medical genetics. Part A》2020,182(5):1273-1277
Autosomal dominant (de novo) mutations in PBX1 are known to cause congenital abnormalities of the kidney and urinary tract (CAKUT), with or without extra‐renal abnormalities. Using trio exome sequencing, we identified a PBX1 p.(Arg107Trp) mutation in a deceased one‐day‐old neonate presenting with CAKUT, asplenia, and severe bilateral diaphragmatic thinning and eventration. Further investigation by droplet digital PCR revealed that the mutation had occurred post‐zygotically in the father, with different variant allele frequencies of the mosaic PBX1 mutation in blood (10%) and sperm (20%). Interestingly, the father had subclinical hydronephrosis in childhood. With an expected recurrence risk of one in five, chorionic villus sampling and prenatal diagnosis for the PBX1 mutation identified recurrence in a subsequent pregnancy. The family opted to continue the pregnancy and the second affected sibling was stillborn at 35 weeks, presenting with similar severe bilateral diaphragmatic eventration, microsplenia, and complete sex reversal (46, XY female). This study highlights the importance of follow‐up studies for presumed de novo and low‐level mosaic variants and broadens the phenotypic spectrum of developmental abnormalities caused by PBX1 mutations. 相似文献
76.
Robert Guidoin PhD Allan R. Downs MD Xavier Barral MD Michel Marois MD Paul-Emile Roy MD Martin King P. Eng Camille Gosselin MD 《Annals of vascular surgery》1986,1(3):369-373
One of the early diamond crimped knitted polyester (Dacron) grafts was surgically excised after implantation for 25 years in the aorto-billiac position because of false aneurysm formation at the three anastomotic sites. The sutures were no longer visible. While the areas around the false aneurysm were poorly incorporated, the graft limbs were well encapsulated with some endothelial-like cells on the luminal surface. The integrity of the graft was well preserved despite mild fraying and the disruption of one stitch. 相似文献
77.
异基因外周血造血干细胞移植后巨细胞病毒间质性肺炎 总被引:1,自引:1,他引:0
目的:探讨异基因外周血造血干细胞移植(Allo-PBSCT)后间质性肺炎(IP)的病因,危险因素及防治方法。方法;将Allo-PBSCT患者分为更昔洛韦(GCV)预防组18例和对照组(未预防组)22例,比较两组巨细胞病毒南性肺炎(CMV-IP)的发生率。结果:对照组Allo-PBSCT患者中并发CMV-IP5例,预防组无1例发生CMV-IP。发生CMV-IP的高危因素为女性供者,合并移植物抗宿主病(GVHD)。4例治愈,1例治疗无效死亡。结论:Allo-PBSCT后CMV感染是IP的主要病因,IP的发生与GVHD严重程度及妇性供者密切相关,GCV能有效预防和治疗CMV-IP。 相似文献
78.
Aleksandra Kukla Mariam P. Alexander Sandor Turkevi‐Nagy Massini Merzkani Walter Park Byron Smith Pingchuan Zhang Xiomara Benavides Matthew D'Costa Catalina Morales Alvarez Aleksandar Denic Andrew Bentall Yogish C. Kudva Mark Stegall 《Clinical transplantation》2021,35(1):e14147
Death with a functioning graft and death‐censored renal allograft failure remain major problems for which effective preventative protocols are lacking. The retrospective cohort study aimed to determine whether histologic changes on a 5‐year surveillance kidney biopsy predict adverse outcomes after transplantation in recipients who had: both Type 2 diabetes (T2DM) and obesity (BMI ≥ 30 kg/m2) at the time of transplantation (T2DM/Obesity, n = 75); neither (No T2DM/No obesity, n = 78); No T2DM/Obesity (n = 41), and T2DM/No obesity (n = 47). On 5‐year biopsies, moderate‐to‐severe mesangial expansion was more common in the T2DM/Obesity group (Banff mm score ≥2 = 49.3%; Tervaert classification MS ≥ 2b = 26.7%) compared to the other groups (p < .001 for both scores). Risk factors included older age, higher BMI, HbA1C, and triglycerides at 1‐year post‐transplant. Moderate‐to‐severe mesangial expansion correlated with death with function (HR 1.74 (1.01, 2.98), p = .045 Banff and 1.89 (1.01, 3.51) p = .045 Tervaert) and with death‐censored graft loss (HR 3.2 (1.2, 8.8), p = .02 Banff and HR 3.8 (1.3, 11.5), p = .01 Tervaert) over a mean of 11.6 years of recipient follow‐up post‐transplant. These data suggest that mesangial expansion in recipients with T2DM and obesity may reflect systemic vascular injury and might be a novel biomarker to predict adverse outcomes post renal transplant. 相似文献
79.
《European journal of medical genetics》2023,66(3):104711
BackgroundHand-Foot-Genital Syndrome (HFGS) is an autosomal dominant disorder characterized by a broad phenotypic spectrum. Variants in HOXA13 gene were associated with HFGS. To date, only twenty families with HFGS have been reported. However, the challenge in HFGS is the limited sample sizes and phenotypic heterogeneity. The advent of next-generation sequencing has permitted the identification of patients with HOXA13 variants who do not manifest with the full HFGS syndromic features.MethodsTrio (parents-proband) Whole-exome sequence(WES) and whole-genome sequencing(WGS) was carried out in this study to investigate the underlying pathogenic genetic factor of the neonate with a wide variety of clinical abnormalities.ResultsNo possible pathogenetic variation was detected by trio-WES, and a duplication variant in HOXA13 (c.360_377dup, p.Ala128_Ala133dup), inherited from her mother, was identified by the subsequent WGS in the proband with malnutrition, feeding difficulties, electrolyte disorders, metabolic acidosis, recurrent urinary tract infections, hydronephrosis, nephrolithiasis, abnormal ureter morphology, cholelithiasis, uterus didelphys. Sequence analysis of the variant region (exon1) indicated a high GC content of 73.92%. In addition, further enquiry of the family history revealed that 5 members of the family in 4 generations had hand and foot anomalies.ConclusionThe neonate was diagnosed with HFGS by genetic analysis. GC content had less influence on sequence coverage in WGS than WES analysis. This was the first report of trio-WGS study for HFGS genetic diagnosis, revealed that subsequent WGS was necessary for identification of potentially pathogenic variants in unexplained genetic disorders. 相似文献
80.
Anselm Frick Ivan Durasin Mechtild Neuweg 《Pflügers Archiv : European journal of physiology》1986,406(4):387-391
Clearance experiments have been performed to study the effects of saline infusion on the reabsorption of inorganic sulfate (SO4) at endogenous levels. Adult female Sprague-Dawley rats on a standard diet were used. Both intact and thyroparathyroidectomized (TPTX) animals were infused with a 130 mmol/l sodium chloride solution at a low (0.15 ml/min) and a high (0.375 ml/min) rate. This increase of the infusion rate decreased the reabsorption of SO4 in both groups of animals significantly. The fractional excretion of SO4 in theintact rats increased from 9.9±5.6 to 18.4±3.6% (mean values±SD,p<0.001) and in theTPTX rats from 5.3±2.5 to 22.4±6.3% (p<0.001). It is concluded that endogenous parathyroid hormone has no major effect on the saline-induced inhibition of reabsorption of SO4.This work was supported by a grant from the Deutsche Forschungsgemeinschaft (Fr 239/9-1) 相似文献