放射免疫疗法可治疗艾滋病


放射免疫疗法可治疗艾滋病

 
 
 
 
 
 
放射免疫疗法可治疗艾滋病
作者:  来源:中国公众科技网  发布者: 刘斌  类别:新闻扫描  日期: 2009-02-26  今日/总浏览: 55/55

  美国耶什华大学阿尔贝特﹒爱因斯坦医学院的科学家将抗体装载到放射性载体上有选择性地摧毁被微生物和HIV感染的细胞。这种放射免疫疗法(RIT)有望能够治疗各种感染性疾病,包括艾滋病和病毒引起的癌症。这是该学院核医学和微生物与免疫学副教授埃卡特琳娜﹒黛德考瓦在美国科学促进会的一次专题研讨会上发表上述观点的。

  

  目前只用于癌症治疗的RIT是利用了一种抗体只针对人体内一种抗原这一特点。把放射性物质与特殊抗体结合,放射就会针对表达相应抗原的细胞,这样就会减少对其他组织的伤害。这种特异性治疗方法是现有放射治疗水平达不到的。

  

  RIT最早是用作癌症治疗而开发,目前在治疗起源于免疫细胞的非霍奇金淋巴瘤上获得很大成功。黛德考瓦在最近几年与微生物和免疫学教授阿托罗﹒卡萨德沃合作改进了这项技术,将它用于治疗真菌、细菌和病毒所引起的感染。

  

  由于病毒与癌症细胞之间差别很大,将放射免疫治疗用于HIV面临很大挑战。病毒是微薄蛋白包裹着DNA或RNA的微小生物。简单、不易被破坏和复原能力强使它很容易摆脱针对它的辐射,而且它还具有快速恢复损伤的能力。更复杂的是,HIV能躲避免疫细胞,使抗体远远达不到它们。

  

  “我们的方法不是以病毒本身为靶子,而是病毒所停留的淋巴细胞。”  黛德考瓦博士说。“幸运的是淋巴细胞属于人体中的放射敏感细胞。”

  

  研究人员设计的这种RIT是由糖蛋白41(gp41)抗体和放射性同位素铋-213与一种特殊配体分子结合组成。选择gp41抗体是因为它与gp41抗原结合后在HIV感染细胞表面能有确切表达。此外,与HIV的其他糖蛋白不同,gp41抗原通常不会进入到血液中,这样放射性标记抗体就不会迷失目标。选择铋-213是因为它有几种特性,包括半衰期为46分钟。如此短的半衰期便于治疗操作,也便于放射性抗体发挥作用。铋-213在4小时后就会消失殆尽。

  

  研究人员证明,这种治疗能有效清除实验室和两个不同HIV小鼠模型中被HIV感染的人类细胞。目前,研究小组正在进行该疗法有效性和安全性的亚临床实验,以便为在HIV患者身上的Ⅰ期临床试验做准备。

  

  RIT还有治疗病毒感染后所引起的癌症的潜质,如宫颈癌(某些与人类乳头状瘤感染有关)和肝癌(与乙型肝炎病毒感染有关)。这些癌症几乎占所有癌症的四分之一。“许多病毒相关癌症会继续表达病毒抗原。”  黛德考瓦博士说。“由于身体其他地方不会有这些抗原,所以RIT治疗病毒相关癌症具有很好的针对性,对患者来说毒性也很低。”  

 
 
作者:
来源: 中国公众科技网
发布者: 刘斌
Radioimmunotherapy can cure AIDS
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Author: Source: China Public Technology Net Posted by: Liu Bin Category: News Scan Date: 2009-02-26 Today View / Total View: 55/55

Albert耶什American University. Albert Einstein College of Medicine scientists will be carrying antibodies to radioactive carriers have selectively destroyed by micro-organisms and HIV infected cells. This Radioimmunotherapy (RIT) is expected to be able to treat infectious diseases, including AIDS and the virus-induced cancer. This is the Institute of nuclear medicine and microbiology and immunology associate professor特琳娜Illueca. Test黛德watts in a AAAS symposium on the above-mentioned viewpoints.

   

Currently only used for the treatment of cancer of the RIT are only made use of an antibody against an antigen that the human body characteristics. Put radioactive material with a special antibody binding, radiation will be aimed at the expression of the corresponding antigen cells, which would reduce the harm to other organizations. This specific treatment methods are the existing level of radiation therapy could not be done.

   

RIT was first developed for cancer treatment, the current in the treatment of immune cells originate from non-Hodgkin's lymphoma received a great success. W黛德test in recent years and Professor of Microbiology and Immunology阿托罗study.卡萨德沃together to improve the technology it used to treat fungal, bacterial and viral infections caused by.

   

Viruses and cancer cells because of the significant differences between the radioimmunotherapy for HIV face a serious challenge. Viruses are small protein DNA or RNA wrapped with tiny biological. Easy, not easy to be destroyed and recovery capability makes it very easy for it out of the radiation, but it also has the ability to quickly resume the injury. Are more complex, HIV can escape the immune cells so that they fall far short of antibodies.

   

"Our approach is not to target the virus itself, but rather stay lymphocyte virus." Rugova said黛德test. "Fortunately lymphocytes belong to the body of the radiation-sensitive cells."

   

Researchers designed this RIT is glycoprotein 41 (gp41) antibody and radioisotope Bismuth -213 with a special composition of ligand molecules. Select gp41 antibody because of its combination with the gp41 antigen in HIV infected cells have the exact expression of surface energy. In addition, with the HIV glycoprotein different from the other, gp41 antigen does not normally enter into the bloodstream, so that the radioactive tag will not lose the target antibody. Bismuth -213 choice because it has several characteristics, including the half-life of 46 minutes. Such a short half-life to facilitate the treatment of the operation, but also easy to play a role in radioactive antibody. Bismuth -213 in 4 hours and will be gone.

   

Researchers have proven that this treatment can effectively clear the laboratory and two different mouse model of HIV were HIV-infected human cells. At present, the Group being the therapy efficacy and safety of sub-clinical trials for HIV patients in Phase Ⅰ Clinical Trial preparation to do.

   

RIT was also the treatment of HIV infection caused by the potential of cancer, such as cervical cancer (some with the human papilloma infection) and liver cancer (with the hepatitis B virus infection). These cancers account for almost a quarter of all cancers. "A lot of virus-related cancer will continue to express viral antigens." Rugova said黛德test. "As in other parts of the body will not have these antigens, so the treatment of virus-related cancer RIT are very good targeted for patients with low toxicity."
 
 
Author:
Source: China Public Technology Net
Posted by: Liu Bin