Journal
EXPERT REVIEW OF VACCINES
Volume 19, Issue 3, Pages 279-292Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/14760584.2020.1745636
Keywords
Vaccine adjuvant; Army Liposome Formulation; ALF; ALFA; ALFQ; AS01; liposomes; monophosphoryl lipid A; QS21; QS-21; malaria vaccine; HIV-1 vaccine; diarrhea vaccine; heroin vaccine
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Funding
- Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. [W81XWH-182-0067]
- US. Department of Defense (DOD) [W81XWH-182-0067]
- Avant Garde award (NIH) [1DP1DA034787-01]
- National Institute on Drug Abuse at NIH [1UG3DA048351-01]
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Introduction: From its earliest days, the US. military has embraced the use of vaccines to fight infectious diseases. The Army Liposome Formulation (ALF) has been a pivotal innovation as a vaccine adjuvant that provides excellent safety and potency and could lead to dual-use military and civilian benefits. For protection of personnel against difficult disease threats found in many areas of the world, Army vaccine scientists have created novel liposome-based vaccine adjuvants. Areas covered: ALF consists of liposomes containing saturated phospholipids, cholesterol, and monophosphoryl lipid A (MPLA) as an immunostimulant. ALF exhibited safety and strong potency in many vaccine clinical trials. Improvements based on ALF include: ALF adsorbed to aluminum hydroxide (ALFA); ALF containing QS21 saponin (ALFQ); and ALFQ adsorbed to aluminum hydroxide (ALFQA). Preclinical safety and efficacy studies with ALF, LFA, ALFQ, and ALFQA are discussed in preparation for upcoming vaccine trials targeting malaria, HIV-1, bacterial diarrhea, and opioid addiction. Expert opinion: The introduction of ALF in the 1980s stimulated commercial interest in vaccines to infectious diseases, and therapeutic vaccines to cancer, and Alzheimer's disease. It is likely that ALF, ALFA, and ALFQ, will provide momentum for new types of modern vaccines with improved efficacy and safety.
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