Synergistic augmentation of CD40-mediated activation of antigen-presenting cells by amphiphilic poly(γ-glutamic acid) nanoparticles.
(2012) In Biomaterials 33(26). p.6230-6239- Abstract
- Agonistic anti-CD40 monoclonal antibodies (mAbs) hold great potential for cancer immunotherapy. However, systemic administration of anti-CD40 mAbs can be associated with severe side effects, such as cytokine release syndrome and liver damage. With the aim to increase the immunostimulatory potency as well as to achieve a local drug retention of anti-CD40 mAbs, we linked an agonistic mAb to immune activating amphiphilic poly(γ-glutamic acid) nanoparticles (γ-PGA NPs). We demonstrate that adsorption of anti-CD40 mAb to γ-PGA NPs (anti-CD40-NPs) improved the stimulatory capacity of the CD40 agonist, resulting in upregulation of costimulatory CD80 and CD86 on antigen-presenting cells, as well as IL-12 secretion. Interestingly, anti-CD40-NPs... (More)
- Agonistic anti-CD40 monoclonal antibodies (mAbs) hold great potential for cancer immunotherapy. However, systemic administration of anti-CD40 mAbs can be associated with severe side effects, such as cytokine release syndrome and liver damage. With the aim to increase the immunostimulatory potency as well as to achieve a local drug retention of anti-CD40 mAbs, we linked an agonistic mAb to immune activating amphiphilic poly(γ-glutamic acid) nanoparticles (γ-PGA NPs). We demonstrate that adsorption of anti-CD40 mAb to γ-PGA NPs (anti-CD40-NPs) improved the stimulatory capacity of the CD40 agonist, resulting in upregulation of costimulatory CD80 and CD86 on antigen-presenting cells, as well as IL-12 secretion. Interestingly, anti-CD40-NPs induced strong synergistic proliferative effects in B cells, possibly resulting from a higher degree of CD40 multimerization, enabled by display of multiple anti-CD40 mAbs on the NPs. In addition, local treatment with anti-CD40-NPs, compared to only soluble CD40 agonist, resulted in a significant reduction in serum levels of IL-6, IL-10, IL-12 and TNF-α in a bladder cancer model. Taken together, our results suggest that anti-CD40-NPs are capable of synergistically enhancing the immunostimulatory effect induced by the CD40 agonist, as well as minimizing adverse side effects associated with systemic cytokine release. This concept of nanomedicine could play an important role in localized immunotherapy of cancer. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/2859534
- author
- Broos, Sissela LU ; Sandin, Linda C ; Apel, Jenny LU ; Tötterman, Thomas H ; Akagi, Takami ; Akashi, Mitsuru ; Borrebaeck, Carl LU ; Ellmark, Peter and Lindstedt, Malin
- organization
- publishing date
- 2012
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Cell, proliferation, Protein adsorption, Immunostimulation, Drug delivery, Nanoparticle
- in
- Biomaterials
- volume
- 33
- issue
- 26
- pages
- 6230 - 6239
- publisher
- Elsevier
- external identifiers
-
- pmid:22687756
- wos:000306720400027
- scopus:84862867187
- pmid:22687756
- ISSN
- 1878-5905
- DOI
- 10.1016/j.biomaterials.2012.05.011
- language
- English
- LU publication?
- yes
- id
- 6a73fb51-ff8b-4385-8d92-1520679dab78 (old id 2859534)
- date added to LUP
- 2016-04-01 10:17:38
- date last changed
- 2022-04-27 20:39:12
@article{6a73fb51-ff8b-4385-8d92-1520679dab78,
abstract = {{Agonistic anti-CD40 monoclonal antibodies (mAbs) hold great potential for cancer immunotherapy. However, systemic administration of anti-CD40 mAbs can be associated with severe side effects, such as cytokine release syndrome and liver damage. With the aim to increase the immunostimulatory potency as well as to achieve a local drug retention of anti-CD40 mAbs, we linked an agonistic mAb to immune activating amphiphilic poly(γ-glutamic acid) nanoparticles (γ-PGA NPs). We demonstrate that adsorption of anti-CD40 mAb to γ-PGA NPs (anti-CD40-NPs) improved the stimulatory capacity of the CD40 agonist, resulting in upregulation of costimulatory CD80 and CD86 on antigen-presenting cells, as well as IL-12 secretion. Interestingly, anti-CD40-NPs induced strong synergistic proliferative effects in B cells, possibly resulting from a higher degree of CD40 multimerization, enabled by display of multiple anti-CD40 mAbs on the NPs. In addition, local treatment with anti-CD40-NPs, compared to only soluble CD40 agonist, resulted in a significant reduction in serum levels of IL-6, IL-10, IL-12 and TNF-α in a bladder cancer model. Taken together, our results suggest that anti-CD40-NPs are capable of synergistically enhancing the immunostimulatory effect induced by the CD40 agonist, as well as minimizing adverse side effects associated with systemic cytokine release. This concept of nanomedicine could play an important role in localized immunotherapy of cancer.}},
author = {{Broos, Sissela and Sandin, Linda C and Apel, Jenny and Tötterman, Thomas H and Akagi, Takami and Akashi, Mitsuru and Borrebaeck, Carl and Ellmark, Peter and Lindstedt, Malin}},
issn = {{1878-5905}},
keywords = {{Cell; proliferation; Protein adsorption; Immunostimulation; Drug delivery; Nanoparticle}},
language = {{eng}},
number = {{26}},
pages = {{6230--6239}},
publisher = {{Elsevier}},
series = {{Biomaterials}},
title = {{Synergistic augmentation of CD40-mediated activation of antigen-presenting cells by amphiphilic poly(γ-glutamic acid) nanoparticles.}},
url = {{http://dx.doi.org/10.1016/j.biomaterials.2012.05.011}},
doi = {{10.1016/j.biomaterials.2012.05.011}},
volume = {{33}},
year = {{2012}},
}