Elsevier

Vaccine

Volume 33, Issue 13, 24 March 2015, Pages 1507-1514
Vaccine

Conference report
Safety of vaccine adjuvants: Focus on autoimmunity

https://doi.org/10.1016/j.vaccine.2015.01.073Get rights and content
Under a Creative Commons license
open access

Highlights

  • Industrial, academic, and governmental experts studied vaccine adjuvants safety.

  • Evidence of signals for autoimmune disorders associated with adjuvants was reviewed.

  • Existing adjuvants (used in marketed vaccines) and novel adjuvants were included.

  • The focus was on oil-in-water emulsion and toll-like receptor agonist adjuvants.

  • No compelling evidence was found associating adjuvants and autoimmunity in humans.

Abstract

Questions have been recently raised regarding the safety of vaccine adjuvants, particularly in relation to autoimmunity or autoimmune disease(s)/disorder(s) (AID). The International Life Sciences Institute (ILSI) Health and Environmental Sciences Institute (HESI) formed a scientific committee and convened a 2-day workshop, consisting of technical experts from around the world representing academia, government regulatory agencies, and industry, to investigate and openly discuss the issues around adjuvant safety in vaccines. The types of adjuvants considered included oil-in-water emulsions and toll-like receptor (TLR) agonists. The state of science around the use of animal models and biomarkers for the evaluation and prediction of AID were also discussed. Following extensive literature reviews by the HESI committee, and presentations by experts at the workshop, several key points were identified, including the value of animal models used to study autoimmunity and AID toward studying novel vaccine adjuvants; whether there is scientific evidence indicating an intrinsic risk of autoimmunity and AID with adjuvants, or a higher risk resulting from the mechanism of action; and if there is compelling clinical data linking adjuvants and AID. The tripartite group of experts concluded that there is no compelling evidence supporting the association of vaccine adjuvants with autoimmunity signals. Additionally, it is recommended that future research on the potential effects of vaccine adjuvants on AID should consider carefully the experimental design in animal models particularly if they are to be used in any risk assessment, as an improper design and model could result in misleading information. Finally, studies on the mechanistic aspects and potential biomarkers related to adjuvants and autoimmunity phenomena could be developed.

Abbreviations

AID
autoimmune disorders
AF
adjuvant formulations
ASIA
autoimmune/inflammatory syndrome induced by adjuvants
CFA
complete Freund′s adjuvant
CIA
collagen-induced arthritis
DA
dark Agouti
DC
dendritic cells
EAE
experimental autoimmune encephalitis
EMA
European Medicines Agency
GWS
Gulf war syndrome
HESI
Health and Environmental Sciences Institute
HLA
human leukocyte antigen
HPV
human papilloma virus
Hsp
heat shock protein
IBD
inflammatory bowel disease
IFA
incomplete Freund′s adjuvant
IFN
interferon
IL
interleukin
ILSI
International Life Sciences Institute
IMI
Innovative Medicines Initiative
MG
myasthenia gravis
miRNA
micro-ribonucleic acid
MMF
macrophagic myofasciitis
MoA
mechanism of action
MPL
monophosphoryl lipid A
mRNA
messenger ribonucleic acid
MS
multiple sclerosis
NOD
non-obese diabetic
O/W
oil-in-water
PAMPs
pathogen associated molecular patterns
PRRs
pattern recognition receptors
PY
person years
RA
rheumatoid arthritis
SjS
Sjögren′s syndrome
SLE
systemic lupus erythematosus
snRNPs
small nuclear ribonucleic particles
TLRs
toll-like receptors
Tregs
regulatory T cells
UTR
untranslated region
W/O
water-in-oil
WOW
water-in-oil-in-water

Keywords

Vaccines
Autoimmunity
Vaccine adjuvants
Animal models
Safety

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