TY - JOUR
T1 - Nanoparticle-induced immune response
T2 - Health risk versus treatment opportunity?
AU - Pondman, Kirsten
AU - le Gac, Séverine
AU - Kishore, Uday
N1 - Funding Information:
I (Kirsten Pondman) would like to thank Professor Bob Sim for his support to my research in the exciting field of immunology and nanotechnology. Bob was a mentor to me from the moment I started working in his lab as an undergraduate student, until long after I finished my PhD research with him. For me, Bob has been an inspiration; I learnt from him how research should be done and how to supervise students with a hands-on approach. He was always kind, knowledgeable, and full of ideas. Always encouraging, but he was also very critical and thorough in reviewing research plans and papers. Bob inspired me to pursue a career in research, encouraged me to follow my own path and provided ample advice not only about research but also on how to combine family life with an academic career, and where priorities should be. He will be greatly missed.
Publisher Copyright:
© 2022 The Authors
PY - 2023/3
Y1 - 2023/3
N2 - Nanoparticles (NPs) are not only employed in many biomedical applications in an engineered form, but also occur in our environment, in a more hazardous form. NPs interact with the immune system through various pathways and can lead to a myriad of different scenarios, ranging from their quiet removal from circulation by macrophages without any impact for the body, to systemic inflammatory effects and immuno-toxicity. In the latter case, the function of the immune system is affected by the presence of NPs. This review describes, how both the innate and adaptive immune system are involved in interactions with NPs, together with the models used to analyse these interactions. These models vary between simple 2D in vitro models, to in vivo animal models, and also include complex all human organ on chip models which are able to recapitulate more accurately the interaction in the in vivo situation. Thereafter, commonly encountered NPs in both the environment and in biomedical applications and their possible effects on the immune system are discussed in more detail. Not all effects of NPs on the immune system are detrimental; in the final section, we review several promising strategies in which the immune response towards NPs can be exploited to suit specific applications such as vaccination and cancer immunotherapy.
AB - Nanoparticles (NPs) are not only employed in many biomedical applications in an engineered form, but also occur in our environment, in a more hazardous form. NPs interact with the immune system through various pathways and can lead to a myriad of different scenarios, ranging from their quiet removal from circulation by macrophages without any impact for the body, to systemic inflammatory effects and immuno-toxicity. In the latter case, the function of the immune system is affected by the presence of NPs. This review describes, how both the innate and adaptive immune system are involved in interactions with NPs, together with the models used to analyse these interactions. These models vary between simple 2D in vitro models, to in vivo animal models, and also include complex all human organ on chip models which are able to recapitulate more accurately the interaction in the in vivo situation. Thereafter, commonly encountered NPs in both the environment and in biomedical applications and their possible effects on the immune system are discussed in more detail. Not all effects of NPs on the immune system are detrimental; in the final section, we review several promising strategies in which the immune response towards NPs can be exploited to suit specific applications such as vaccination and cancer immunotherapy.
KW - Adaptive immune system
KW - Immune models
KW - Immune response
KW - Innate immune system
KW - Nanoparticles
KW - UT-Gold-D
UR - http://www.scopus.com/inward/record.url?scp=85145287405&partnerID=8YFLogxK
U2 - 10.1016/j.imbio.2022.152317
DO - 10.1016/j.imbio.2022.152317
M3 - Article
C2 - 36592542
AN - SCOPUS:85145287405
SN - 0171-2985
VL - 228
JO - Immunobiology
JF - Immunobiology
IS - 2
M1 - 152317
ER -