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1.
用BA-ELISA斑点法检测痢疾杆菌免疫小鼠GALT中的特异性抗体分泌细胞(ASC) 总被引:1,自引:0,他引:1
改进的BA-ELISPOT法使免疫酶斑更为清晰,保存时间延长。用此法检测了痢疾杆菌福氏2a经口及腹腔免疫后,小鼠派伊尔氏(PP)淋巴结、肠系膜淋巴结(MLN)及脾脏(SPL)中特异性IgA、IgG、IgM抗体分泌细胞(AntibodySecretingcell,ASC)的动态变化,得到有规律的结果:两种免疫途径均能在PP及MLN中诱导出3类特异ASC的显著升高,但口服导致的升高其持续时间较腹腔途径为短。此外,腹腔途径还能诱导SPL中3种ASC升高。 相似文献
2.
The 2001 Bethesda system (TBS 2001) eliminated the "satisfactory but limited by" category, benign cellular changes (BCC), and the designations "favor benign" (ASC-B) and "favor low grade" (ASC-L) for atypical squamous cells. We compared the unsatisfactory rate and atypical squamous cells:squamous intraepithelial lesions (ASC:SIL) ratio pre- and postimplementation of TBS 2001 to see if there was an increase in unsatisfactory specimens, ASC rate, and altered ASC:SIL ratio. Pap Tests (569,726) reviewed at the Cytopathology Laboratory of Women and Infants Hospital from 1998-2002 were included. TBS 1991 terminology was used through December 31, 2001. Conversion to TBS 2001 took place on January 1, 2002. The average ASC:SIL ratios pre- and postimplementation of TBS 2001 were 1.52:1 and 1.42:1, respectively. The rates of unsatisfactory specimens and ASC remained unchanged. Conversion to TBS 2001 did not adversely affect the ASC:SIL ratio or the detection rates of abnormalities of Pap tests. 相似文献
3.
目的探索维甲酸诱导甲状腺癌细胞的凋亡情况及凋亡相关斑点样蛋白(ASC)的表达。方法甲状腺滤泡状癌细胞株FIE-133(A组),乳头状甲状腺癌细胞株W3(B组),未分化甲状腺癌细胞株8505C(c组),3组细胞用维甲酸刺激24h共同培养。流式细胞术观察细胞活性,RT—PCR和Western blotting检测ASCmRNA及蛋白的表达。采用双向电泳分离蛋白质,采用PDQuest2-DE软件分析维甲酸+A组与A组细胞2组间差异表达的蛋白质斑点,并用Western blotting进一步验证。结果流式细胞术结果,维甲酸均导致3组细胞凋亡,A组的凋亡率强于B、C2组(P〈0.01)。RT—PCR和Western blotting检测的ASC mRNA及蛋白的表达,A、B、C3组均有表达,A组强于B、C2组(P〈0.05)。维甲酸作用A组,质谱鉴定了ASC蛋白.Western blotting验证蛋白质ASC与双向电泳的结果一致。结论为维甲酸治疗甲状腺癌的蛋白质研究提供实验资料。 相似文献
4.
Bovine paratuberculosis is a highly prevalent chronic infection of the small intestine in cattle, caused by Mycobacterium avium subspecies paratuberculosis (MAP). In earlier studies we showed the protective effect of Hsp70/DDA subunit vaccination against paratuberculosis. In the current study we set out to measure primary immune responses generated at the site of Hsp70 vaccination. Lymph vessel cannulation was performed to obtain efferent lymph from the prescapular lymph node draining the neck area where the vaccine was applied. Hsp70 vaccination induced a significant increase of CD21+ B cells in efferent lymph, accounting for up to 40% of efferent cells post-vaccination. Proliferation (Ki67+) within the CD21+ B cell and CD4+ T cell populations peaked between day 3 and day 5 post-vaccination. From day 7, Hsp70-specific antibody secreting cells (ASCs) could be detected in efferent lymph. Hsp70-specific antibodies, mainly of the IgG1 isotype, were also detected from this time point onwards. However, post-vaccination IFN-γ production in efferent lymph was non-sustained. In conclusion, Hsp70-vaccination induces only limited Th1 type immune responsiveness as reflected in efferent lymph draining the vaccination site. This is in line with our previous observations in peripheral blood. The main primary immunological outcome of the Hsp70/DDA subunit vaccination is B cell activation and abundant Hsp70-specific IgG1 production. This warrants the question whether Hsp70-specific antibodies contribute to the observed protective effect of Hsp70 vaccination in calves. 相似文献
5.
Vision is the sense that we use to navigate the world around us. Thus it is not surprising that blindness is one of people's most feared maladies. Heritable diseases of the retina, such as age-related macular degeneration and retinitis pigmentosa, are the leading cause of blindness in the developed world, collectively affecting as many as one-third of all people over the age of 75, to some degree. For decades, scientists have dreamed of preventing vision loss or of restoring the vision of patients affected with retinal degeneration through drug therapy, gene augmentation or a cell-based transplantation approach. In this review we will discuss the use of the induced pluripotent stem cell technology to model and develop various treatment modalities for the treatment of inherited retinal degenerative disease. We will focus on the use of iPSCs for interrogation of disease pathophysiology, analysis of drug and gene therapeutics and as a source of autologous cells for cell transplantation and replacement. 相似文献
6.
7.
Suzanne M. Selvaggi M.D 《Diagnostic cytopathology》2013,41(11):943-946
Atypical squamous cells, cannot exclude high grade squamous intraepithelial lesion (ASC‐H) is a recognized category in the 2001 Bethesda Nomenclature System for cervical cytology. Although current ASCCP guidelines recommend colposcopic follow‐up, more recent studies are suggesting prior triage for HPV‐DNA analysis. We report on our experience at the University of Wisconsin Hospital and Clinics. From January 1, 2003 through December 31, 2011 (9‐y), the cytopathology laboratory processed 109,424 Pap Tests, of which 281 (0.26%) were diagnosed as ASC‐H. Tissue follow‐up was available in 181 (64%) of these cases, of which 45 (25%) were negative/cervicitis, 41 (23%) were CIN 1, 36 (20%) were CIN 2 and 59 (32%) were CIN 3. Stratification by age groups showed a higher percentage of high grade (CIN 2+) lesions (65%) in the premenopausal age group as compared with high grade lesion (35%) in the postmenopausal age group, whereas negative/CIN1 biopsies were more common in postmenopausal (65%) as compared to premenopausal (44%) women. Our data support the use of colposcopy in the management of women with ASC‐H on Pap Tests. However, in the older age group, prior HPV‐DNA testing may be of benefit to better identify those women at risk for high grade lesions. Diagn. Cytopathol. 2013;41:943–946. © 2013 Wiley Periodicals, Inc. 相似文献
8.
Distribution of human endogenous retrovirus type W receptor in normal human villous placenta 总被引:5,自引:0,他引:5
BACKGROUND: The fusion of trophoblast cells into the villous syncytiotrophoblast is crucial for appropriate placental function and fetal development. Fusion occurs following the interaction of syncytin-1, an envelope protein of the endogenous retrovirus HERV-W, and the RD114/mammalian type D retrovirus receptor (RDR/ASCT2) on adjacent cell membranes. This process must be tightly regulated in order to maintain the proliferative pool of cytotrophoblast cells as well as the function of the syncytia. AIM: We sought to investigate whether syncytial fusion of placental cytotrophoblast cells may be regulated via modulation of RDR/ASCT2 expression. METHODS: Expression of RDR/ASCT2 in term and first trimester villous placenta was assessed along with a number of molecular markers using immunofluorescent staining. In a complementary approach, Western blotting was used to investigate RDR/ASCT2 expression in a panel of choriocarcinoma cell lines before and after stimulation of fusion. RESULTS: Villous placental RDR/ASCT2 expression was found to be restricted to the cytotrophoblast compartment, being largely absent in the syncytiotrophoblast. Local variations in RDR/ASCT2 expression were not associated with the proliferative status of cytotrophoblast cells. RDR/ASCT2 expression was also shown to be down-regulated in BeWo choriocarcinoma cells after stimulation of syncytial fusion. CONCLUSION: This first report of the localisation and distribution of RDR/ASCT2 in human placental villi suggests that the fusion of placental trophoblast cells is not regulated by local or temporal variations of RDR/ASCT2 expression in villous cytotrophoblast cells. 相似文献
9.
《Vaccine》2018,36(41):6191-6201
Liposomal vaccines incorporating adjuvant and CD4 T cell helper peptides enhance antibody responses against weakly immunogenic B cell epitopes such as found in the membrane proximal external region (MPER) of the HIV-1 gp41 subunit. While the inclusion of exogenous helper peptides in vaccine formulations facilitates stronger and more durable antibody responses, the helper peptide incorporation strategy per se may influence the overall magnitude and quality of B cell target antigen immunogenicity. Both variability in individual peptide encapsulation as well as the potential for liposome surface-associated helper peptides to misdirect the humoral response are potential parameters impacting outcome. In this study, we used MPER/liposome vaccines as a model system to examine how the mode of the potent LACK T helper peptide formulation modulates antibody responses against the MPER antigen. We directly compared liposome surface-arrayed palmitoyl LACK (pLACK) versus soluble LACK (sLACK) encapsulated in the liposomes and free in solution. Independent of LACK formulation methods, dendritic cell activation and LACK presentation were equivalent in vivo. The frequency of MPER-specific GC B cells promoted by sLACK was higher than that stimulated by pLACK formulation, a finding associated with a significantly greater frequency of LACK-specific GC B cells induced by pLACK. While there were no significant differences in the quantity of MPER-specific serological responses, the MPER-specific antibody titer trended higher with sLACK formulated vaccines at the lower dose of LACK. However, pLACK generated relatively greater MPER-specific antibody affinities than those induced by sLACK-formulated vaccines. Overall, the results suggest that liposomal surface-associated LACK enhances immunogenicity of LACK through better engagement of LACK-specific B cells. Of note, this is not detrimental to the induction of MPER-specific immune responses; rather, the elicitation of higher affinity anti-MPER antibodies benefits from augmented help delivered via covalent linkage of the pLACK CD4 T cell epitope in conjunction with MPER/liposome presentation. 相似文献
10.
目的探究甘草酸对幼鼠实验性结肠炎的治疗作用及其作用机制。方法将75只SD大鼠幼鼠随机分为对照组、模型组、柳氮磺胺吡啶组(0.5 g/kg)和甘草酸40、160 mg/kg组,每组各15只,制备实验性结肠炎模型的同时分别灌肠给药,连续7 d。观察大鼠一般情况,HE染色法观察大鼠结肠组织病理学变化并进行疾病活动指数(DAI)评分、黏膜损伤指数(CMDI)评定,酶联免疫法测定血清中白介素-4(IL-4)、白介素-17(IL-17)、白介素-1β(IL-1β)水平,逆转录-聚合酶链反应(RT-PCR)、Western blotting法检测大鼠结肠组织中NLRP3、白介素-1β(IL-1β)、凋亡相关斑点样蛋白(ASC)、半胱天冬酶(caspase-1)表达。结果与模型组比较,甘草酸组幼鼠体质量逐渐增加,症状改善;炎症细胞浸润有所减少,腺体破坏程度降低;DAI评分、CMDI评分均降低,呈剂量相关性(P0.05);IL-4水平升高,IL-17、IL-1β水平降低,呈剂量相关性(P0.05);NLRP3、ASC、caspase-1、IL-1βmRNA表达和蛋白表达均降低,呈剂量相关性(P0.05)。结论甘草酸能够治疗大鼠实验性结肠炎,可能与抑制NLRP3通路蛋白表达、降低炎症因子水平有关。 相似文献