Kee-Jong Hong

Prof. Dr. Kee-Jong Hong

orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2017 in Clinical and Experimental Vaccine Research
Verified
Journal Article
Open access
PDF file
KKKi Mun Kwon
Ki Mun Kwon
SLSu-Min Lim
Su-Min Lim
SCSeulgi Choi
Seulgi Choi
DKDa-Hee Kim
Da-Hee Kim
HJHee-Eun Jin
Hee-Eun Jin
JKJoo Young Kim
Joo Young Kim
Kwon KM, et al. Clin Exp Vaccine Res. 2017 Jul;6(2):156-159. https://doi.org/10.7774/cevr.2017.6.2.156

1 January 2015 in Clinical and Experimental Vaccine Research
Verified
Journal Article
Open access
PDF file
WCWoo Young Choi
Woo Young Choi
KHKee-Jong Hong
Kee-Jong Hong
JHJoo Eun Hong
Joo Eun Hong
WLWon-Ja Lee
Won-Ja Lee
Choi WY, et al. Clin Exp Vaccine Res. 2015 Jan;4(1):11-16. http://dx.doi.org/10.7774/cevr.2015.4.1.11

21 March 2025 in Vaccines
Verified
Journal Article
Open access
PDF file
MFMunazza Fatima
Munazza Fatima
KHKee-Jong Hong
Kee-Jong Hong
Combination vaccines provide the versatile benefits of addressing different pathogens simultaneously using a combined formulation. This approach can be regarded as a substantial modernization in immunization. In this review, we highlight various advancements in combination vaccines based on mRNA, viral vectors, live attenuated, and recombinant vaccines. Recent success in clinical trials of mRNA platforms for combination vaccines has particularly accelerated research in this direction. The advantages of combination vaccines in terms of patient adherence, cost effectiveness, and streamlined immunization schedule are discussed. The existing challenges of antigenic interference, logistical hurdles, and the complications of regulatory standards are analyzed. Research trends to make combination vaccines viable for emerging infections have been summarized. The current work provides a critical overview, the existing opportunities, and the future prospects of combination vaccines.

1 March 2025 in Biomolecules
Verified
Journal Article
Open access
PDF file
MFMunazza Fatima
Munazza Fatima
TATimothy An
Timothy An
KHKee-Jong Hong
Kee-Jong Hong
Modernization of existing methods for the delivery of mRNA is vital in advanced therapeutics. Traditionally, mRNA has faced obstacles of poor stability due to enzymatic degradation. This work examines cutting-edge formulation and emerging techniques for safer delivery of mRNA vaccines. Inspired by the success of lipid nanoparticles (LNP) in delivering mRNA vaccines for COVID-19, a variety of other formulations have been developed to deliver mRNA vaccines for diverse infections. The meritorious features of nanoparticle-based mRNA delivery strategies, including LNP, polymeric, dendrimers, polysaccharide-based, peptide-derived, carbon and metal-based, DNA nanostructures, hybrid, and extracellular vesicles, have been examined. The impact of these delivery platforms on mRNA vaccine delivery efficacy, protection from enzymatic degradation, cellular uptake, controlled release, and immunogenicity has been discussed in detail. Even with significant developments, there are certain limitations to overcome, including toxicity concerns, limited information about immune pathways, the need to maintain a cold chain, and the necessity of optimizing administration methods. Continuous innovation is essential for improving delivery systems for mRNA vaccines. Future research directions have been proposed to address the existing challenges in mRNA delivery and to expand their potential prophylactic and therapeutic application.

1 January 2019 in Clinical and Experimental Vaccine Research
Verified
Journal Article
Open access
BSByoung-Shik Shim
Byoung-Shik Shim
KHKee-Jong Hong
Kee-Jong Hong
PMPuna Maya Maharjan
Puna Maya Maharjan
SCSunghwa Choe
Sunghwa Choe
Vaccination is one of the most successful strategies to prevent diseases caused by pathogens. Although various expression systems including Escherichia coli, yeast, insect, and mammalian cells are currently used for producing many of vaccines, these conventional platforms have the limitation of post-translational modification, high cost, and expensive scalability. In this respect, the plant-based expression system has been considered as an attractive platform to produce recombinant vaccines due to fast, cost-effective and scalable production as well as safety. This review discusses the development of plant-derived vaccines and the current stage of plant-based expression system.

1 January 2018 in Clinical and Experimental Vaccine Research
Verified
Journal Article
Open access
PDF file
KHKee-Jong Hong
Kee-Jong Hong
SSSang-Hwan Seo
Sang-Hwan Seo
Hong KJ, et al. Clin Exp Vaccine Res. 2018 Jul;7(2):145-148. https://doi.org/10.7774/cevr.2018.7.2.145