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Immunity首次揭示树突细胞识别外源物机制有望开发下一代疫苗 [复制链接]

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发表于 2012-4-9 22:33 |只看该作者 |倒序浏览 |打印


Immunity:首次揭示树突细胞识别外源物机制有望开发下一代疫苗






预测性的人CLEC9A二维结构(S:半胱氨酸残基;Y:酪氨酸残基),图片来自Cristal Huysamen et al. CLEC9A Is a Novel .树突细胞在外来入侵物---比如病毒、细菌和寄生物以及肿瘤细胞和其他死亡或受损的细胞---侵入身体时发出警报过程中发挥着关键性作用。它们也被称作抗原呈递细胞,能够消化和呈递来自受损细胞的分子到其他的免疫细胞以便识别外源入侵物和发动免疫应答。

来自澳大利亚沃尔特与伊丽莎-霍尔研究所(Walter and Eliza Hall Institute)的Mireille Lahoud博士、Jian-Guo Zhang博士和Peter Czabotar博士和Ken Shortman教授领导的一个研究小组首次鉴定出在树突细胞表面发现的一个蛋白如何识别能够代表感染的危险性损伤。相关研究结果于2012年4月5日发表在《细胞》子刊Immunity期刊上,并证实免疫系统进化出一种特别聪明的方法来检测受损的细胞和死亡的细胞从而有助于产生免疫应答。
在之前的研究中,研究人员已经鉴定出一种被称作Clec9A (C-type lectin domain family 9A,即C型凝集素结构域家族成员9A)的蛋白,该蛋白存在于特定类型的树突细胞表面上,对受损的细胞和死亡的细胞作出反应。在这项研究中,研究人员发现Clec9A识别和结合到肌动蛋白纤维上,其中肌动蛋白是在体内所有细胞中发现的细胞内部蛋白。只有当细胞膜受到损伤或破坏时,肌动蛋白才暴露出来,因此它是一个完美的方法来发现容纳潜在危险性感染的细胞并让它们暴露在免疫系统的作用下。
Shortman教授说,能够利用Clec9A产生一种新类型的更加现代的疫苗,而且这种疫苗更加有效,但是副作用更小。Clec9A蛋白是当前已知的改善免疫应答的最好靶标之一。通过创建能够结合到Clec9A的疫苗,人们就能够诱导树突细胞认为它们遭遇到受损的细胞从而有助于对传染原发动免疫应答。
Shortman教授说,“靶向蛋白Clec9A能够降低实际所需的疫苗量至100到1000倍。传统的产生免疫性的疫苗技术,如使用灭活的全病毒或寄生物来激发机体产生免疫识别功能,需要大量疫苗以期它遇到正确的免疫细胞,而且它还需要加入其他的物质(即佐剂)以便提示免疫系统有外来物来袭。我们正提出一种新类型的疫苗:它能够直接前往合适的细胞从而有助于促进免疫应答,同时又不导致传统疫苗产生的副作用,因为它的特异性更强。”
Lahoud博士说,对于当前没有好的预防措施的疾病如疟疾或HIV而言,这项发现能够有助于提高用于预防这些疾病发生的疫苗的有效性。人们也可能利用免疫系统开发出治疗性疫苗来治疗和预防疾病如一些类型的癌症。


doi:10.1016/j.immuni.2012.03.009
PMC:
PMID:

The Dendritic Cell Receptor Clec9A Binds Damaged Cells via Exposed Actin Filaments
Jian-Guo Zhang, Peter E. Czabotar, Antonia N. Policheni, Irina Caminschi, Soo San Wan, Susie Kitsoulis, Kirsteen M. Tullett, Adeline Y. Robin, Rajini Brammananth, Mark F. van Delft, Jinhua Lu, Lorraine A. O'Reilly, Emma C. Josefsson, Benjamin T. Kile, Wei Jin Chin, Justine D. Mintern, Maya A. Olshina, Wilson Wong, Jake Baum, Mark D. Wright, David C.S. Huang, Narla Mohandas, Ross L. Coppel, Peter M. Colman, Nicos A. Nicola, Ken Shortman, Mireille H. Lahoud
The immune system must distinguish viable cells from cells damaged by physical and infective processes. The damaged cell-recognition molecule Clec9A is expressed on the surface of the mouse and human dendritic cell subsets specialized for the uptake and processing of material from dead cells. Clec9A recognizes a conserved component within nucleated and nonnucleated cells, exposed when cell membranes are damaged. We have identified this Clec9A ligand as a filamentous form of actin in association with particular actin-binding domains of cytoskeletal proteins. We have determined the crystal structure of the human CLEC9A C-type lectin domain and propose a functional dimeric structure with conserved tryptophans in the ligand recognition site. Mutation of these residues ablated CLEC9A binding to damaged cells and to the isolated ligand complexes. We propose that Clec9A provides targeted recruitment of the adaptive immune system during infection and can also be utilized to enhance immune responses generated by vaccines.





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发表于 2012-4-10 07:18 |只看该作者
间接的好消息

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发表于 2012-4-10 11:24 |只看该作者
等试验成功,再临床几期,外国本地成功生产了,再打入中国,又需要几年的临床检验,这样又得10年或以上时间吧,那时候大家的青春早已···

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发表于 2012-4-10 20:50 |只看该作者
本帖最后由 StephenW 于 2012-4-10 20:51 编辑

        News
                        
               

                                       
                                        Discovery could improve vaccines                        
                                        Walter and Eliza Hall Institute                                          
                Tuesday, 10 April 2012        


Researchers have discovered how a vital immune cell recognises dead and damaged body cells, a find that could help them create 'next-generation' vaccines.Image: plrang/iStockphoto


The discovery of how a vital immune cell recognises dead and damaged body cells could modernise vaccine technology by ‘tricking’ cells into launching an immune response, leading to next-generation vaccines that are more specific, more effective and have fewer side-effects.

Scientists from the Walter and Eliza Hall Institute have identified, for the first time, how a protein found on the surface of immune cells called dendritic cells recognises dangerous damage and trauma that could signify infection.

Dendritic cells are critical for raising the alarm about the presence of foreign invaders in the body such as viruses, bacteria and parasites as well as tumour cells and other dead or damaged cells. Also known as antigen-presenting cells, they digest and present molecules from damaged cells to other immune cells that recognise foreign invaders and launch an immune response.

The research was a collaborative effort that involved a team of immunologists, protein chemists and structural biologists. The research team was led by Dr Mireille Lahoud (formerly from the Immunology division), Dr Jian-Guo Zhang (Cancer and Haematology division), Dr Peter Czabotar (Structural Biology division) and Professor Ken Shortman (Immunology division).

Dr Lahoud said the study, published today in the journal Immunity, demonstrated that the immune system has evolved a very clever way of detecting damaged and dead cells to help promote an immune response.

“Dr Irina Caminschi and I previously identified a protein called Clec9A (C-type lectin domain family 9A) that sits on the surface of specialised types of dendritic cells and responds to damaged and dying cells,” Dr Lahoud said. “In this study we discovered that Clec9A recognises and binds to fibres of actin, internal cell proteins that are found in all cells of the body. Actin is only exposed when the cell membrane is damaged or destroyed, so it is an excellent way of finding cells that could harbour potentially dangerous infections and exposing them to the immune system.”

Professor Shortman said that exploiting Clec9A could be used to generate a new, more modern class of vaccines that are more effective and have fewer side-effects. “The Clec9A protein is one of the best targets currently known for improving immune responses,” he said. “By creating vaccines that bind to Clec9A, we can trick dendritic cells to think they have encountered a damaged cell and help to launch an immune response to the infectious agent of our choice.”

Professor Shortman said targeting Clec9A could decrease the amount of vaccine needed by 100 to 1000 times. “Traditional vaccine technology for generating immunity, such as using inactivated whole viruses or parasites for immune recognition, requires large amounts of vaccine in the hopes it will encounter the correct immune cells, and incorporates other substances (adjuvants) that are needed to signal to the immune system that something foreign is happening. We are proposing a new type of vaccine that we know will head directly to the right cell to help stimulate an immune response, and doesn’t cause the same side-effects because it is more specific,” Professor Shortman said.

Dr Lahoud said that the finding could develop or increase the efficacy of vaccines for diseases that do not currently have good preventive options, such as malaria, or HIV. “There is also the possibility that the system could be used to develop therapeutic vaccines for treating diseases, such as some forms of cancer, as well as for preventing them,” she said.

Since completing this research, Dr Lahoud and Dr Caminschi have accepted positions at the Burnet Institute.

This work was supported by the National Health and Medical Research Council of Australia, the Australian Research Council and the Victorian Government.

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