TY - JOUR
T1 - Vaccine Development against the Renin-Angiotensin System for the Treatment of Hypertension
AU - Azegami, Tatsuhiko
AU - Itoh, Hiroshi
N1 - Funding Information:
This work was supported in part by the Japan Society for the Promotion of Science (Grant no. 25870715) and Keio Gijuku Academic Development Funds
Funding Information:
-is work was supported in part by the Japan Society for the Promotion of Science (Grant no. 25870715) and Keio Gijuku Academic Development Funds.
Publisher Copyright:
© 2019 Tatsuhiko Azegami and Hiroshi Itoh.
PY - 2019
Y1 - 2019
N2 - Hypertension is a global public health issue and the most important preventable cause of cardiovascular diseases. Despite the clinical availability of many antihypertensive drugs, many hypertensive patients have poor medication adherence and blood pressure control due, at least partially, to the asymptomatic and chronic characteristics of hypertension. Immunotherapeutic approaches have the potential to improve medication adherence in hypertension because they induce prolonged therapeutic effects and need a low frequency of administration. The first attempts to reduce blood pressure by using vaccines targeting the renin-angiotensin system were made more than half a century ago; however, at the time, a poor understanding of immunology and the mechanisms of hypertension and a lack of optimal vaccine technologies such as suitable antigen design, proper adjuvants, and effective antigen delivery systems meant that attempts to develop antihypertensive vaccines failed. Recent advances in immunology and vaccinology have provided potential therapeutic immunologic approaches to treat not only infectious diseases but also cancers and other noncommunicable diseases. One important biotechnology that has had a major impact on modern vaccinology is virus-like particle technology, which can efficiently deliver vaccine antigens without the need for artificial adjuvants. A human clinical trial that indicated the effectiveness and safety of a virus-like particle-based antiangiotensin II vaccine marked a turning point in the field of therapeutic antihypertensive vaccines. Here, we review the history of the development of immunotherapies for the treatment of hypertension and discuss the current perspectives in the field.
AB - Hypertension is a global public health issue and the most important preventable cause of cardiovascular diseases. Despite the clinical availability of many antihypertensive drugs, many hypertensive patients have poor medication adherence and blood pressure control due, at least partially, to the asymptomatic and chronic characteristics of hypertension. Immunotherapeutic approaches have the potential to improve medication adherence in hypertension because they induce prolonged therapeutic effects and need a low frequency of administration. The first attempts to reduce blood pressure by using vaccines targeting the renin-angiotensin system were made more than half a century ago; however, at the time, a poor understanding of immunology and the mechanisms of hypertension and a lack of optimal vaccine technologies such as suitable antigen design, proper adjuvants, and effective antigen delivery systems meant that attempts to develop antihypertensive vaccines failed. Recent advances in immunology and vaccinology have provided potential therapeutic immunologic approaches to treat not only infectious diseases but also cancers and other noncommunicable diseases. One important biotechnology that has had a major impact on modern vaccinology is virus-like particle technology, which can efficiently deliver vaccine antigens without the need for artificial adjuvants. A human clinical trial that indicated the effectiveness and safety of a virus-like particle-based antiangiotensin II vaccine marked a turning point in the field of therapeutic antihypertensive vaccines. Here, we review the history of the development of immunotherapies for the treatment of hypertension and discuss the current perspectives in the field.
UR - http://www.scopus.com/inward/record.url?scp=85071690705&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85071690705&partnerID=8YFLogxK
U2 - 10.1155/2019/9218531
DO - 10.1155/2019/9218531
M3 - Review article
AN - SCOPUS:85071690705
SN - 2090-0384
VL - 2019
JO - International Journal of Hypertension
JF - International Journal of Hypertension
M1 - 9218531
ER -