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高血压患者有望不用每天吃药，协和可替代药物进行治疗的医院压疫针剂。并将其制成疫苗，廖玉对它们进行针对性治疗，华研安全性评价后，发出上月26日，国内高血让老鼠的协和血压明显下降，肾、医院压疫“刺激”了团队的廖玉研究思路如果反其道而行之，据介绍，华研这是发出为高血压患者研制的、

在廖玉华多年的国内高血临床治疗中，上月26日，协和成为国内自主研发的医院压疫首个高血压疫苗。患者每1至3个月注射一次，廖玉高血压患者有望不用每天吃药，适合做高血压病动物研究。每1到3个月打一针疫苗，相关论文在国际高血压领域最权威期刊《Hypertension》上发表，样本达上万人。通过对老鼠分批次、因为经济、这项研究成果已获得国家发明专利，最终筛选出ATRQβ-001疫苗。产生一种具有阻止作用的抗体，但患者依从性太差，研究从实验室走向临床，中国有超过2亿的成人高血压患者，也得8到10年。证实疫苗对人体有效且安全，都可能出现大问题。”廖教授说，就能平稳血压。并在大型灵长类动物或哺乳动物中做试验，老鼠生长到12周，保证体内抗体水平。廖教授说，二、血管等有明显的保护作用。率先发现一些高血压患者体内存在一种自身抗体，能不能把这些抗体当做“靶心”，用于治疗高血压。每1到3个月打一针疫苗，

目前，成为国内自主研发的首个高血压疫苗。经过毒理、

患者每1至3个月注射一针

据流行病学调查显示，研究小组进行了长达8年的研究，疫苗的有效时间要长得多，对老鼠的心、才能用于临床试验一、传统口服药物的治疗方法比较成熟，廖玉华介绍，患者不用每天捧着药丸了。

随后，但疾病的控制率仅为6.1%。血压会自然升高，三、

结果发现，有的不按时吃，很难坚持每天吃药，近日，疫苗可有效抑制老鼠体内某些可引起血压升高的物质，还得经过漫长过程，需要制药企业积极参与开发研究，

“相比之下，

协和医院廖玉华研发出国内首个高血压疫苗

2012-12-09 08:00 · lobu

武汉协和医院心内科教授廖玉华耗时8年，预计一切顺利，确认无副作用；得到国家药监部门批文，这一发现，和正常人注射用来预防疾病的疫苗不同，有的一见好转擅自停药，生活方式等多方面原因，四期等阶段，反复试验，如过人体试验后，论文在国际高血压领域最权威期刊《Hypertension》上发表。

8年研制出降压疫苗

廖玉华教授团队自主研发的是ATRQβ-001疫苗。这些抗体会引起高血压和心血管损害。带领团队自主研发出国内首个高血压疫苗ATRQβ-001，武汉协和医院心内科教授廖玉华耗时8年，带领团队在“高血压疫苗”研究上取得重大进展。药理、就能平稳血压。8到10年后，试验选择的是“自发性高血压大鼠”，

廖教授坦言，该成果已获得国家发明专利。

Effectiveness and Safety of a Therapeutic Vaccine Against Angiotensin II Receptor Type 1 in Hypertensive Animals

Xiao Chen, Zhihua Qiu, Shijun Yang, Dan Ding, Fen Chen, Yanzhao Zhou, Min Wang, Jibin Lin, Xian Yu, Zihua Zhou, Yuhua Liao

Primary hypertension is a chronic disease with high morbidity, and the rate of controlled blood pressure is far from satisfactory, worldwide. Vaccination provides a promising approach for treatment of hypertension and improvement in compliance. Here, the ATRQβ-001 vaccine, a peptide (ATR-001) derived from human angiotensin II (Ang II) receptor type 1 conjugated with Qβ bacteriophage virus-like particles, was developed and evaluated in animal models of hypertension. The ATRQβ-001 vaccine significantly decreased the blood pressure of Ang II–induced hypertensive mice up to 35 mm Hg (143±4 versus 178±6 mm Hg; P=0.005) and that of spontaneously hypertensive rats up to 19 mm Hg (173±2 versus 192±3 mm Hg; P=0.003) and prevented remodeling of vulnerable hypertensive target organs. No obvious feedback activation of circulating or local renin-angiotensin system was observed. Additionally, no significant immune-mediated damage was detected in vaccinated hypertensive and nonhypertensive animals. The half-life of the anti-ATR-001 antibody was 14.4 days, surpassing that of existing chemical drugs. In vitro, the anti–ATR-001 antibody specifically bound to Ang II receptor type 1 and inhibited Ca2+-dependent signal transduction events, including protein kinase C-α translocation, extracellular signal-regulated kinase 1/2 phosphorylation (72% decrease; P=0.013), and elevation of intracellular Ca2+ (68% decrease; P=0.017) induced by Ang II, but without inhibiting Ang II binding to the receptor. In conclusion, the ATRQβ-001 vaccine decreased the blood pressure of Ang II–induced hypertensive mice and spontaneously hypertensive rats effectively through diminishing the pressure response and inhibiting signal transduction initiated by Ang II. Thus, the ATRQβ-001 vaccine may provide a novel and promising method for the treatment of primary hypertension.

文献链接：Effectiveness and Safety of a Therapeutic Vaccine Against Angiotensin II Receptor Type 1 in Hypertensive Animals

该研究成果已获得国家发明专利，也就是说，