Dental acrylates and methacrylates - Interactions with the immune system
Abstract
Professionals working in dentistry have reported adverse effects, such as allergic contact dermatitis due to
exposure to different methacrylates/acrylates. Leakage of such monomers from dental fillings due to incomplete
curing is also common. Monomers are released into the oral cavity and some may also diffuse through
the dentin and reach the dental pulp. In the tissue, monomers will come in contact with different cells of the
immune system. At present, there is a lack of knowledge of the effects these monomers might have on cells.
The main objective of this thesis was to investigate possible effects of four different methacrylate/acrylate
monomers on the immune system in vivo and in vitro. The studied methacrylates and acrylate were ethyl
methacrylate (EMA), diethylene glycol diacrylate (DEGDA), 2-hydroxyethyl methacrylate (HEMA) and
triethylene glycol dimethacrylate (TEGDMA). In summary, our in vivo and in vitro results showed that:
• HEMA affects the immune system by inducing formation of the NLRP3 inflammasome (Study
I).
• TEGDMA has adjuvant properties and the ability to modulate cytokine production from peripheral
blood mononuclear cells, which may lead to interference with the normal immune response
to various agents, self or non-self, present in the pulp and the oral mucosa (Study II).
• HEMA acts as a mucosal adjuvant when applied sublingually together with ovalbumin (OVA) or
Streptococcus mutans in mice (Study III).
• The different monomers affect the production, increase as well as decrease, of various cytokines
in vitro by peripheral blood mononuclear cells. Antibody production and T cell activity to OVA
was increased in mice immunized with OVA in combination with methacrylates (Study IV).
Bacteria and bacterial products such as hydrogen sulfide (H2S) challenge the oral mucosa. We wanted to
investigate whether H2S also affects the immune system in similar way as HEMA, i.e., induce formation of
the NLRP3 inflammasome.
• Human mononuclear leukocytes exposed to H2S had an enhanced production of NLRP3 inflammasome-
dependent secretion of IL-1β and IL-18. (Study V). Thus, this may be a mode for H2S
to contribute to the inflammatory host response and pathogenesis of periodontal disease
In summary, the different methacrylate/acrylate monomers frequently used in dental restoration materials
may interfere with the immune system in many different ways. The increase as well as the decrease in
cytokine production from human mononuclear cells is affected by all these methacryleate/acrylate monomers.
The T and B cell activity is also affected by all tested methacrylates . Thus, this may be a model that
provide some insight into the nature of the immune responses to methacrylates and acrylates, and may
advance the development of more biocompatible restorative materials in the future for clinical use.
Parts of work
I. Alizadehgharib S, Östberg AK, Larsson L and Dahlgren U. The immunomodulatory
properties of 2-hydroxyethyl methacrylate are mediated by the NLRP3 inflammasome.
Submitted for publication. II. Alizadehgharib S, Östberg AK and Dahlgren U. Triethylene glycol dimethacrylate –
adjuvant properties and effect on cytokine production. Submitted for publication. III. Östberg AK, Alizadehgharib S and Dahlgren U. Sublingual administration of 2-
hydroxyethyl methacrylate enhances antibody responses to co-administered ovalbumin
and Streptococcus mutans. Submitted for publication. IV. Alizadehgharib S, Östberg AK and Dahlgren U. Effects of the methacrylate/acrylate
monomers HEMA, TEGDMA, DEGDA and EMA on the immune system. Submitted for
publication. V. Basic A, Alizadehgharib S, Dahlén G and Dahlgren U. Hydrogen Sulfide exposure
induces NLRP3 inflammasome-dependent IL-1β and IL-18 secretion in human mononuclear
leukocytes in vitro. Clinical and Experimental Dental Research 2017. 3:115-120. ::doi::10.1002/cre2.69
Degree
Doctor of Philosophy (Odontology)
University
University of Gothenburg. Sahlgrenska Academy
Institution
Institute of Odontology. Department of Oral Microbiology
Disputation
Fredagen den 27 oktober 2017, kl. 13.00, Föreläsningssal 3, Odontologen, Medicinaregatan 12D, Göteborg
Date of defence
2017-10-27
Sara.Alizadehgharib@gu.se
Date
2017-10-10Author
Alizadehgharib, Sara
Keywords
Acrylates
Methacrylates
Antibodies
NLRP3 inflammasome
Cytokines
Mice
Hydrogen sulfide
Publication type
Doctoral thesis
ISBN
ISBN 978-91-629-0245-2 (PDF)
ISBN 978-91-629-0244-5 (Print)
Language
eng