Biodegradable Cationic Polycarbonates as Vaccine Adjuvants
Source abstract
Abstract
In this study, biodegradable cationic polycarbonate and polylactide block copolymers were synthesized and successfully used as novel vaccine adjuvants to provide enhanced anticancer immunity. The polymers formed nanoparticles with the model vaccine, ovalbumin (OVA), and the immunostimulant toll-like receptor 3 agonist poly(I:C) (a synthetic analog of the double-stranded RNA). Higher uptake of poly(I:C) by the bone marrow-derived dendritic cells and macrophages and OVA by dendritic cells was observed when delivered using the polymer adjuvant. In vivo experiments showed that these nanoparticles remained longer in the subcutaneous injection site as compared to OVA alone and led to higher production of anti-OVA specific antibodies with prolonged immunostimulation. When OVA was combined with poly(I:C) that was either co-entrapped in the same particles or as separate particles, a comparable level of anti-OVA IgG1 antibodies and interleukin-6 (IL-6) was produced in mouse blood plasma, and a similar level of cytotoxic T lymphocyte (CTL) response in mice was stimulated as compared to OVA/Alum particles. Furthermore, tumor rejection in the mice that were vaccinated for 9 months with the formulations containing the polymer adjuvant was stronger than the other treatment groups without the polymer. Notably, the cationic polycarbonates were not associated with any adverse in vivo effects. Thus, these biodegradable polymers may be promising substitutes for aluminum-based adjuvants in vaccine formulations.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Immunotherapy and Immune Responses · RNA Interference and Gene Delivery · Immune Cell Function and Interaction
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Bioengineering and Nanotechnology, 31 Biopolis Way, The Nanos, Singapore 138669, Singapore
NanoBio Lab, 31 Biopolis Way, #09-01 The Nanos, Singapore 138669, Singapore
IBM Almaden Research Center, 650 Harry Road, San Jose, California 95120 United States
Funding
International Business Machines Corporation · Agency for Science, Technology and Research
References (59)
Show source-provided references
1. Mohan T. · Indian J. Med. Res. · 2013 · 138 · 779
2. 10.1073/pnas.080808910510.1073/pnas.0808089105 ↗
3. 10.1038/cti.2016.1910.1038/cti.2016.19 ↗
4. 10.3390/vaccines302032010.3390/vaccines3020320 ↗
5. 10.1126/science.107106510.1126/science.1071065 ↗
6. 10.1016/j.immuni.2007.02.01110.1016/j.immuni.2007.02.011 ↗
7. 10.1111/j.1600-065X.2012.01124.x10.1111/j.1600-065X.2012.01124.x ↗
8. Davila E. · Cancer Res. · 2003 · 63 · 3281
9. Ulrich J. T. · 1995 · 49510.1007/978-1-4615-1823-5_21 ↗
10. 10.1016/0006-291X(74)90640-810.1016/0006-291X(74)90640-8 ↗
11. 10.1016/j.vaccine.2006.03.07110.1016/j.vaccine.2006.03.071 ↗
12. 10.1016/j.vaccine.2009.01.11810.1016/j.vaccine.2009.01.118 ↗
13. 10.1016/s0264-410x(96)00055-210.1016/s0264-410x(96)00055-2 ↗
14. 10.1586/14760584.1.1.11110.1586/14760584.1.1.111 ↗
15. 10.1111/j.1440-1711.2004.01293.x10.1111/j.1440-1711.2004.01293.x ↗
16. 10.1016/S0264-410X(01)00456-X10.1016/S0264-410X(01)00456-X ↗
17. 10.1016/0264-410X(92)90356-O10.1016/0264-410X(92)90356-O ↗
18. Hunter R. · J. Immunol. · 1981 · 127 · 124410.4049/jimmunol.127.3.1244 ↗
19. 10.1016/j.immuni.2007.11.00310.1016/j.immuni.2007.11.003 ↗
20. 10.1186/s40413-015-0060-510.1186/s40413-015-0060-5 ↗
21. Gupta R. K. · 1995 · 22910.1007/978-1-4615-1823-5_8 ↗
22. 10.1099/jmm.0.038943-010.1099/jmm.0.038943-0 ↗
23. 10.1016/j.tips.2009.03.00510.1016/j.tips.2009.03.005 ↗
24. 10.1007/s40264-015-0350-410.1007/s40264-015-0350-4 ↗
25. Shakya A. K. · J. Biosci, Biotechnol. · 2012 · 1
26. 10.1016/j.biomaterials.2017.03.03410.1016/j.biomaterials.2017.03.034 ↗
27. 10.1021/acsbiomaterials.8b0159110.1021/acsbiomaterials.8b01591 ↗
28. 10.1016/j.biomaterials.2014.10.04310.1016/j.biomaterials.2014.10.043 ↗
29. Hunter R. · The Journal of Immunology · 1984 · 133 · 316710.4049/jimmunol.133.6.3167 ↗
30. 10.1016/0161-5890(91)90076-V10.1016/0161-5890(91)90076-V ↗
31. 10.1080/02652049928879910.1080/026520499288799 ↗
32. 10.1016/j.jconrel.2015.02.00610.1016/j.jconrel.2015.02.006 ↗
33. 10.1021/acs.molpharmaceut.7b0079510.1021/acs.molpharmaceut.7b00795 ↗
34. 10.1016/j.jconrel.2011.01.02010.1016/j.jconrel.2011.01.020 ↗
35. 10.1016/j.actbio.2017.03.02710.1016/j.actbio.2017.03.027 ↗
36. 10.1016/j.biomaterials.2007.11.02110.1016/j.biomaterials.2007.11.021 ↗
37. 10.1007/s00253-006-0488-110.1007/s00253-006-0488-1 ↗
38. 10.1002/mabi.20070010610.1002/mabi.200700106 ↗
39. 10.1039/B713925J10.1039/B713925J ↗
40. 10.1021/ma061607o10.1021/ma061607o ↗
41. 10.1016/j.biomaterials.2019.01.03610.1016/j.biomaterials.2019.01.036 ↗
42. 10.1016/j.biomaterials.2008.10.06210.1016/j.biomaterials.2008.10.062 ↗
43. 10.1016/j.nano.2019.10205610.1016/j.nano.2019.102056 ↗
44. 10.1016/j.cocis.2014.10.00210.1016/j.cocis.2014.10.002 ↗
45. Lv H. · J. Controlled Release · 2006 · 114 · 10010.1016/j.jconrel.2006.04.014 ↗
46. 10.1039/C6TB01556E10.1039/C6TB01556E ↗
47. 10.1038/srep2749410.1038/srep27494 ↗
48. 10.4049/jimmunol.175.3.137310.4049/jimmunol.175.3.1373 ↗
49. Flaherty D. K. · 2012
50. 10.1016/S0278-6915(99)00159-310.1016/S0278-6915(99)00159-3 ↗
51. 10.1016/0008-8749(89)90263-310.1016/0008-8749(89)90263-3 ↗
52. 10.1080/21645515.2014.100402610.1080/21645515.2014.1004026 ↗
53. 10.1093/ilar.43.Suppl_1.S3110.1093/ilar.43.Suppl_1.S31 ↗
54. 10.1111/j.1745-7254.2008.00889.x10.1111/j.1745-7254.2008.00889.x ↗
55. 10.1093/jmcb/mjp00110.1093/jmcb/mjp001 ↗
56. Martínez-Lostao L. · 201510.1158/1078-0432.CCR-15-0685 ↗
57. Janeway C. A. · 2001 · 2
58. 10.1016/j.intimp.2011.05.01410.1016/j.intimp.2011.05.014 ↗
59. Fisher, D. T.; Appenheimer, M. M.; Evans, S. S. In The Two Faces of Il-6 in the Tumor Microenvironment, Seminars in Immunology, Elsevier: 2014; pp. 38–47.10.1016/j.smim.2014.01.008 ↗