Immune Netw.  2004 Sep;4(3):131-142. 10.4110/in.2004.4.3.131.

A Current Research Insight into Function and Development of Adjuvants

Affiliations
  • 1Department of Information Analysis, Korea Institute of Science and Technology Information (KISTI), Cheongryangri-dong, Dongdaemun-gu, Seoul, Korea.
  • 2Department of Pharmacognosy Material Development, Samcheok National University, Samcheok, Kangwon-do, Korea.
  • 3Division of Immunopharmacology, College of Pharmacy, Sungkyunkwan University, Suwon, Kyunggi-do, Korea. snpyo@skku.ac.kr

Abstract

In recent years, adjuvants have received much attention because of the development of purified subunit and synthetic vaccines which are poor immunogens and require adjuvants to evoke the immune response. Therefore, immunologic adjuvants have been developed and testing for most of this century. During the last years much progress has been made on development, isolation and chemical synthesis of alternative adjuvants such as derivatives of muramyl dipeptide, monophosphoryl lipid A, liposomes, QS-21, MF-59 and immunostimulating complexes (ISCOMS). Biodegradable polymer microspheres are being evaluated for targeting antigens on mucosal surfaces and for controlled release of vaccines with an aim to reduce the number of doses required for primary immunization. The most common adjuvants for human use today are aluminum hydroxide and aluminum phosphate. Calcium phosphate and oil emulsions have been also used in human vaccination. The biggest issue with the use of adjuvants for human vaccines is the toxicity and adverse side effects of most of the adjuvant formulations. Other problems with the development of adjuvants include restricted adjuvanticity of certain formulations to a few antigens, use of aluminum adjuvants as reference adjuvant preparations under suboptimal conditions, non-availability of reliable animal models, use of non-standard assays and biological differences between animal models and humans leading to the failure of promising formulations to show adjuvanticity in clinical trials. The availability of hundreds of different adjuvants has prompted a need for identifying rational standards for selection of adjuvant formulations based on safety and sound immunological principles for human vaccines. The aim of the present review is to put the recent findings into a broader perspective to facilitate the application of these adjuvants in general and experimental vaccinology.

Keyword

Adjuvant; animal model; human vaccines; oil emulsions; microspheres

MeSH Terms

Acetylmuramyl-Alanyl-Isoglutamine
Adjuvants, Immunologic
Aluminum
Aluminum Hydroxide
Calcium
Emulsions
Humans
Immunization
ISCOMs
Lipid A
Liposomes
Microspheres
Models, Animal
Polymers
Vaccination
Vaccines
Vaccines, Synthetic
Acetylmuramyl-Alanyl-Isoglutamine
Adjuvants, Immunologic
Aluminum
Aluminum Hydroxide
Calcium
Emulsions
ISCOMs
Lipid A
Liposomes
Polymers
Vaccines
Vaccines, Synthetic
Full Text Links
  • IN
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr