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1.
Th17细胞和Treg细胞是CD4+T细胞的新亚群,在分化发育、功能发挥的过程中受到Th1型、Th2型效应细胞以及自身分泌产生细胞因子的调节,参与自身免疫病、感染、肿瘤等疾病的发生发展。通过对Th17和Treg分化发育、和功能发挥过程中的关键调节因子进行阻断或加强,可以上调或下调Th17和Treg在疾病中的表达,以用于疾病的预防和诊治。  相似文献   

2.
Th17细胞是新近发现的第三类CD4+ T辅助细胞亚群,其所分泌的IL-17、IL-22等细胞因子在中性粒细胞趋化、组织重塑与修复及介导抗体蛋白的产生等具有重要作用.但Th17分化调节受外界环境影响较大,如转录因子、细胞因子、Th1、Th2和调节T细胞(Tregs)等,这些均具有决定初始CD4+ T细胞向Th17细胞的分化方向和免疫反应方向的调控作用.目前Th17在器官移植物免疫耐受中的作用越来越受到重视,明确Th17分化调节的各种影响因素,将为器官移植免疫耐受研究提供新思路.  相似文献   

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Th17细胞是近年来被发现的一种不同于Th1和Th2细胞并产生IL-17的Th细胞亚群,它具有独立的分化和发育调节机制.Th17的发育、扩增及分泌IL-17主要受TGF-β,IL-6,IL-23等细胞因子的调控.IL-17调节前炎性因子、趋化因子等的产生及分泌,在白细胞的迁移、破骨细胞的活化和骨质的吸收等方面发挥重要作用,并在自身免疫性疾病和感染性疾病中发挥重要调节作用.本综述主要介绍Th17细胞分化的影响因素、产生的细胞因子和在自身免疫病中的作用.  相似文献   

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我国是乙型肝炎病毒(HBV)高感染率国家,乙型肝炎发病机制十分复杂,宿主免疫调节紊乱是导致不能有效清除病毒、病情迁延不愈的重要原因,其中CD4+T淋巴细胞发挥主要作用。最近,新发现的CD4+T细胞的几种亚群为乙型肝炎致病机制的研究提供了新思路。这些新的T细胞亚群中,有一种被称为Th17细胞,表达转录因子ROR-γt,并分泌各种IL-17因子参与免疫反应。另一种为Treg细胞,表达转录因子Fox P3,主要分泌TGF-β因子,当TGF-β单独存在时,初始的效应T细胞分化为Treg细胞。辅助性Th17细胞(Th17)和调节性T细胞(regulatory T cell,Treg)在分化发育、增殖及功能上有着密切的联系,并参与乙型肝炎的致病过程,对乙型肝炎的发生、发展、及愈后有一定影响。最近的研究表明,Th17/Treg的失调可能参与了乙型肝炎的异常免疫反应,从而导致慢性炎症的形成和HBV的持续感染。本文就Th17细胞和Treg细胞及其失衡在乙型肝炎致病机制中的作用予以综述,为乙型肝炎的免疫学治疗提供理论基础。  相似文献   

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近年研究发现了效应性辅助性T细胞的新亚群-Th17细胞,它主要分泌IL-17、IL-17F、IL-21和IL-22等细胞因子。Th17细胞及其效应分子被认为与自身免疫病和其他多种疾病相关。该文从Th17细胞的发现、人和小鼠Th17细胞的分化、Th17细胞的效应性因子及与健康和疾病的相关性几个方面对目前的研究进展进行了综述。  相似文献   

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CD4+CD25+FOXP3+的调节T细胞(regulatory T cells,Treg)在维持机体免疫平衡方面起着重要的作用。体外扩增Treg细胞用于治疗自身免疫病、哮喘及诱导器官移植免疫耐受引起人们极大的兴趣。Treg细胞可分为2个亚群,分别为nTreg和iTreg,两者有不同的生物学特性。nTreg在特定条件下,可以分泌具有促进炎症的IL-17;iTreg在体内可丢失FOXP3,失去其免疫抑制功能。Treg细胞用于临床治疗,还有许多问题需要研究解决。  相似文献   

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目的:探讨在实验性自身免疫性脑脊髓炎(EAE)治疗中TGF-β与IL-6介导的骨髓基质干细胞(BMSCs)的双向调节作用与机制。方法:分离纯化BMSCs,并与EAE大鼠动物模型淋巴细胞共培养,应用抗TGF-β和IL-6单克隆抗体封闭TGF-β或IL-6通路,ELISA检测不同比例MSC与淋巴细胞共培养中对细胞因子的作用,流式细胞仪检测MSC对Th细胞亚群分化的影响,过继免疫临床评分检测BMSC治疗中的关键通路。结果:1:10比例BMSCs共培养组与对照组相比,IL-17分泌量下降(P0.05),Treg细胞显著增高(P0.05)而Th17细胞显著降低(P0.05),共培养后的淋巴细胞进行过继免疫回输后,1:10干细胞共培养组临床评分显著降低(P0.05),而1:100比例共培养组与上述结果相反,中和TGF-β和IL-6抗体可以调节此免疫作用。结论:BMSCs通过TGF-β和IL-6通路调节免疫系统调节性T细胞(Treg)和Th17的细胞平衡,此过程与BMSCs剂量密切相关,本研究可为干细胞更好的临床应用提供理论基础。  相似文献   

8.
罗飞  李志英 《生命科学》2012,(4):346-349
Th17细胞是近年发现的一种新型CD4^+效应性T细胞,以其特异性的分泌IL-17而命名。介导免疫耐受的Treg细胞和介导炎症反应的Th17细胞间功能和分化过程相互对抗,在正常状态下,两者保持平衡,但机体发生功能异常时常表现出Treg/Th17失衡,引起炎性反应、自身免疫性疾病、移植物抗宿主病等的发生和发展,并决定疾病的转归和预后,在肿瘤免疫中亦发挥了重要作用。该文就Treg/Th17失衡在肿瘤,尤其是子宫颈癌发生发展中的作用进行综述。  相似文献   

9.
Th17细胞及Th17/Treg失衡在炎症反应、组织损伤及纤维化形成中发挥了重要作用,与多种疾病的发生发展密切相关。前炎性细胞因子可诱导T细胞分化为Th17,使Th17/Treg失衡,导致IL-17、IL-6、趋化因子等促炎性细胞因子大量分泌并有效介导中性粒细胞动员与兴奋,使得机体产生炎症反应与免疫病理反应。就Th17/Treg细胞及其失衡在肝脏免疫病理反应中的研究进展进行了综述。  相似文献   

10.
多发性骨髓瘤(MM)系血液系统的恶性肿瘤,以老年人多见.目前治疗以化疗和自身干细胞移植为主,仍难以治愈.多发性骨髓瘤的进展涉及到一系列基因和骨髓微环境的改变,这些改变恰好促进了肿瘤细胞的生长并瓦解了局部的免疫反应.CD4+和CD8+T细胞在多发性骨髓瘤患者体内数量和功能的改变都已经阐明.Treg细胞和Th17细胞的平衡在维持多发性骨髓瘤患者的抗肿瘤免疫中起着至关重要的作用.Treg细胞负责维持机体对外来抗原和自身抗原的免疫耐受.Th17细胞主要参与机体抵抗真菌和寄生虫感染、炎症反应和自身免疫.多发性骨髓瘤患者体内TGF-β和IL-6高水平表达,并可直接或通过其他促炎因子影响Th17细胞的分化,进而调节机体的抗肿瘤免疫应答.因此我们针对Treg细胞和Th17细胞在多发性骨髓瘤中的研究进展进行阐述.  相似文献   

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It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.  相似文献   

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Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.  相似文献   

18.
Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.  相似文献   

19.
肝癌中HBV和HCV基因和抗原的分布及意义   总被引:1,自引:0,他引:1  
采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细  相似文献   

20.
For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment.  相似文献   

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