Eui-Cheol Shin

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Eui-Cheol Shin
Born (1971-08-29) August 29, 1971 (age 52)
Seoul, Korea
Occupation(s)Medical immunologist, academic, and author
Academic background
EducationDoctor of Medicine
M.S. Microbiology and Immunology
Ph.D. Microbiology and Immunology
Alma materYonsei University College of Medicine
Academic work
InstitutionsKorea Advanced Institute of Science and Technology (KAIST)
Institute for Basic Science
Korean name
Hangul
신의철
Revised RomanizationShin Uicheol
McCune–ReischauerShin Ŭich'ŏl

Eui-Cheol Shin (Korean: 신의철; born August 29, 1971) is a South Korean medical immunologist, academic, and author. He is a professor at the Graduate School of Medical Science and Engineering at the Korea Advanced Institute of Science and Technology (KAIST),[1] and director of The Center for Viral Immunology at the Institute for Basic Science (IBS), a Korean government-funded research institute.[2]

Shin's research focus lies in the field of medical immunology with a particular focus on T cell responses to viral infection and cancer and T cell-mediated immunopathogenesis.[3]

Shin is a Fellow of the Korean Academy of Science and Technology.[4][5] He is Deputy Editor of Immune Network.[6]

Education

Shin completed his Doctor of Medicine from Yonsei University College of Medicine in 1996. He then pursued a Master's degree in Microbiology and Immunology from the same university and completed it in 1998. He completed his PHD in Microbiology and Immunology from the Yonsei University College of Medicine in 2001.[1]

Career

Shin joined the Immunology Section, Liver Diseases Branch, at the National Institute of Diabetes and Digestive and Kidney Diseases, NIH as a research fellow in 2002 and served until 2007. In 2007, he joined the Graduate School of Medical Science and Engineering, KAIST, as an assistant professor and served there for a period of six years up until 2013. From 2013 to 2018, he was appointed associate professor at the Graduate School of Medical Science and Engineering, KAIST. As of 2018, he is a professor at the Graduate School of Medical Science and Engineering, KAIST and an adjunct professor at the Yonsei University College of Medicine.[2]

Shin was a director at The Center for Epidemic Preparedness, KAIST, from 2020 to 2021. He has been a director at the Center for Viral Immunology, Korea Virus Research Institute, Institute for Basic Science.[2]

Research

Shin has authored numerous publications, including articles in peer-reviewed journals. His research interests span the fields of medical immunology with a particular focus on T cell responses to viral infection and cancer and immunopathogenesis.[3]

Bystander T cell activation

Shin discovered a pathological significance of bystander T cell activation in human viral disease by studying T cell responses in patients infected with hepatitis A virus (HAV). He found that pre-existing bystander memory CD8+ T cells are unexpectedly activated by cytokines (e.g., IL-15) regardless of their antigen specificity, causing liver cell damage through NKG2D-mediated cytotoxicity.[7] This study demonstrated for that bystander T cells can be a cause of host injury in human viral infection. In subsequent studies, he characterized IL-15-responsive bystander T cells in the liver microenvironment.[8][9][10] In addition, he revealed a mechanism of IL-15 production from epithelial cells[11] and found CD5 as a major negative regulator of IL-15-induced T cell proliferation.[12] His theory about bystander T cell activation has been highlighted as an important pathological mechanism in human viral disease.[13]

Immune responses in COVID-19

During the COVID-19 pandemic, Shin studied immune responses to COVID-19. First, he revealed a mechanism of hyper-inflammation in patients with severe COVID-19 by performing single-cell RNA-seq analysis.[14] In his study, he reported a paradoxical role of type I IFNs in exacerbating inflammation in COVID-19 patients.[15] He also performed a detailed characterization of SARS-CoV-2-specific CD8+ T cells, revealing that despite expressing PD-1, they are functionally active and not exhausted.[16] These findings corrected the misinformation that had been previously reported during the early stages of the COVID-19 pandemic. This was one of the first studies that detected SARS-CoV-2-specific CD8+ T cells using MHC class I multimers. In addition, he demonstrated that SARS-CoV-2-specific T cell memory is sustained for a long period after recovery from COVID-19 with the successful development of stem cell-like memory T cells.[17] Moreover, he showed that memory T cells elicited by COVID-19 mRNA vaccination substantially respond to the Omicron variant.[18] On the basis of his findings, he proposed T cell-oriented strategies for controlling the COVID-19 pandemic.[19]

Awards and honors

  • 2016: GSK Academic Award, The Korean Association for the Study of the Liver
  • 2017: Hantan Award, The Korea Society of Virology
  • 2018: KAI-Genexine Award, The Korean Association of Immunologists
  • 2019: Yongwoon Grand Prize in Medicine, Yonsei University College of Medicine & Yongwoon Foundation
  • 2022: Asan Award in Medicine, Asan Foundation[20]

Bibliography

Selected articles

  • Kim, J., Chang, D. Y., Lee, H. W., Lee, H., Kim, J. H., Sung, P. S., ... & Shin, E. C. (2018). Innate-like cytotoxic function of bystander-activated CD8+ T cells is associated with liver injury in acute hepatitis A. Immunity, 48(1), 161–173.
  • Lee, J. S., Park, S., Jeong, H. W., Ahn, J. Y., Choi, S. J., Lee, H., ... & Shin, E. C. (2020). Immunophenotyping of COVID-19 and influenza highlights the role of type I interferons in development of severe COVID-19. Science immunology, 5(49), eabd1554.
  • Rha, M. S., Jeong, H. W., Ko, J. H., Choi, S. J., Seo, I. H., Lee, J. S., ... & Shin, E. C. (2021). PD-1-expressing SARS-CoV-2-specific CD8+ T cells are not exhausted, but functional in patients with COVID-19. Immunity, 54(1), 44–52.
  • Noh, J. Y., Jeong, H. W., Kim, J. H., & Shin, E. C. (2021). T cell-oriented strategies for controlling the COVID-19 pandemic. Nature Reviews Immunology, 21(11), 687–688.
  • Koh, J. Y., Rha, M. S., Choi, S. J., Lee, H. S., Han, J. W., Nam, H., ... & Shin, E. C. (2022). Identification of a distinct NK-like hepatic T-cell population activated by NKG2C in a TCR-independent manner. Journal of hepatology, 77(4), 1059–1070.
  • Jung, M. K., Jeong, S. D., Noh, J. Y., Kim, D. U., Jung, S., Song, J. Y., ... & Shin, E. C. (2022). BNT162b2-induced memory T cells respond to the Omicron variant with preserved polyfunctionality. Nature Microbiology, 7(6), 909–917.

References

  1. ^ a b "PROFESSOR - Laboratory of Immunology and Infectious Diseases".
  2. ^ a b c "Director - Center for Viral Immunology".
  3. ^ a b "Eui-Cheol Shin". scholar.google.com.
  4. ^ 회원소개 - Eui Cheol, Shin [Member Introduction - Eui Cheol, Shin]. Korean Academy of Science and Technology (in Korean). Retrieved 2 March 2024.
  5. ^ "(Director 2024) Center for Viral Immunology / Korea Virus Research Institute - Institute for Basic Science".
  6. ^ ":: Immune Network ::". www.immunenetwork.org.
  7. ^ Kim, Jihye; Chang, Dong-Yeop; Lee, Hyun Woong; Lee, Hoyoung; Kim, Jong Hoon; Sung, Pil Soo; Kim, Kyung Hwan; Hong, Seon-Hui; Kang, Wonseok; Lee, Jino; Shin, So Youn; Yu, Hee Tae; You, Sooseong; Choi, Yoon Seok; Oh, Insoo; Lee, Dong Ho; Lee, Dong Hyeon; Jung, Min Kyung; Suh, Kyung-Suk; Hwang, Shin; Kim, Won; Park, Su-Hyung; Kim, Hyung Joon; Shin, Eui-Cheol (January 16, 2018). "Innate-like Cytotoxic Function of Bystander-Activated CD8+ T Cells Is Associated with Liver Injury in Acute Hepatitis A". Immunity. 48 (1): 161–173.e5. doi:10.1016/j.immuni.2017.11.025. PMID 29305140. S2CID 633138.
  8. ^ Kim, Jong Hoon; Han, Ji Won; Choi, Young Joon; Rha, Min-Seok; Koh, June Young; Kim, Kyung Hwan; Kim, Chang Gon; Lee, Yong Joon; Kim, A. Reum; Park, Junsik; Kim, Hong Kwan; Min, Byung Soh; Seo, Seong Il; Kang, Minyong; Park, Hye Jung; Han, Dai Hoon; Kim, Soon Il; Kim, Myoung Soo; Lee, Jae Geun; Lee, Dong Hyeon; Kim, Won; Park, Jun Yong; Park, Su-Hyung; Joo, Dong Jin; Shin, Eui-Cheol (June 5, 2020). "Functions of human liver CD69+CD103-CD8+ T cells depend on HIF-2α activity in healthy and pathologic livers". Journal of Hepatology. 72 (6): 1170–1181. doi:10.1016/j.jhep.2020.01.010. PMID 31987989. S2CID 210933853 – via PubMed.
  9. ^ Rha, Min-Seok; Han, Ji Won; Kim, Jong Hoon; Koh, June-Young; Park, Hye Jung; Kim, Soon Il; Kim, Myoung Soo; Lee, Jae Geun; Lee, Hyun Woong; Lee, Dong Hyeon; Kim, Won; Park, Jun Yong; Joo, Dong Jin; Park, Su-Hyung; Shin, Eui-Cheol (September 5, 2020). "Human liver CD8+ MAIT cells exert TCR/MR1-independent innate-like cytotoxicity in response to IL-15". Journal of Hepatology. 73 (3): 640–650. doi:10.1016/j.jhep.2020.03.033. PMID 32247824. S2CID 214811567 – via PubMed.
  10. ^ "Identification of a distinct NK-like hepatic T-cell population activated by NKG2C in a TCR-independent manner - Journal of Hepatology".
  11. ^ Kim, Tae-Shin; Rha, Min-Seok; Shin, Eui-Cheol (January 15, 2022). "IFN-γ Induces IL-15 Trans-Presentation by Epithelial Cells via IRF1". Journal of Immunology. 208 (2): 338–346. doi:10.4049/jimmunol.2100057. PMID 34893528. S2CID 245035902.
  12. ^ "CD5 Suppresses IL-15–Induced Proliferation of Human Memory CD8+ T Cells by Inhibiting mTOR Pathways - The Journal of Immunology".
  13. ^ Lee, Hoyoung; Jeong, Seongju; Shin, Eui-Cheol (August 5, 2021). "Significance of bystander T cell activation in microbial infection". Nature Immunology. 23 (1): 13–22. doi:10.1038/s41590-021-00985-3. PMID 34354279. S2CID 236933989.
  14. ^ Lee, Jeong Seok; Park, Seongwan; Jeong, Hye Won; Ahn, Jin Young; Choi, Seong Jin; Lee, Hoyoung; Choi, Baekgyu; Nam, Su Kyung; Sa, Moa; Kwon, Ji-Soo; Jeong, Su Jin; Lee, Heung Kyu; Park, Sung Ho; Park, Su-Hyung; Choi, Jun Yong; Kim, Sung-Han; Jung, Inkyung; Shin, Eui-Cheol (July 10, 2020). "Immunophenotyping of COVID-19 and influenza highlights the role of type I interferons in development of severe COVID-19". Science Immunology. 5 (49): eabd1554. doi:10.1126/sciimmunol.abd1554. PMC 7402635. PMID 32651212.
  15. ^ Lee, Jeong Seok; Shin, Eui-Cheol (October 5, 2020). "The type I interferon response in COVID-19: implications for treatment". Nature Reviews. Immunology. 20 (10): 585–586. doi:10.1038/s41577-020-00429-3. PMC 8824445. PMID 32788708.
  16. ^ Rha, Min-Seok; Jeong, Hye Won; Ko, Jae-Hoon; Choi, Seong Jin; Seo, In-Ho; Lee, Jeong Seok; Sa, Moa; Kim, A. Reum; Joo, Eun-Jeong; Ahn, Jin Young; Kim, Jung Ho; Song, Kyoung-Ho; Kim, Eu Suk; Oh, Dong Hyun; Ahn, Mi Young; Choi, Hee Kyoung; Jeon, Ji Hoon; Choi, Jae-Phil; Kim, Hong Bin; Kim, Young Keun; Park, Su-Hyung; Choi, Won Suk; Choi, Jun Yong; Peck, Kyong Ran; Shin, Eui-Cheol (January 12, 2021). "PD-1-Expressing SARS-CoV-2-Specific CD8+ T Cells Are Not Exhausted, but Functional in Patients with COVID-19". Immunity. 54 (1): 44–52.e3. doi:10.1016/j.immuni.2020.12.002. PMC 7834198. PMID 33338412.
  17. ^ Jung, Jae Hyung; Rha, Min-Seok; Sa, Moa; Choi, Hee Kyoung; Jeon, Ji Hoon; Seok, Hyeri; Park, Dae Won; Park, Su-Hyung; Jeong, Hye Won; Choi, Won Suk; Shin, Eui-Cheol (June 30, 2021). "SARS-CoV-2-specific T cell memory is sustained in COVID-19 convalescent patients for 10 months with successful development of stem cell-like memory T cells". Nature Communications. 12 (1): 4043. Bibcode:2021NatCo..12.4043J. doi:10.1038/s41467-021-24377-1. PMC 8245549. PMID 34193870. S2CID 235698573.
  18. ^ Jung, Min Kyung; Jeong, Seong Dong; Noh, Ji Yun; Kim, Dong-Uk; Jung, Sungmin; Song, Joon Young; Jeong, Hye Won; Park, Su-Hyung; Shin, Eui-Cheol (June 5, 2022). "BNT162b2-induced memory T cells respond to the Omicron variant with preserved polyfunctionality". Nature Microbiology. 7 (6): 909–917. doi:10.1038/s41564-022-01123-x. PMID 35577972. S2CID 248831658.
  19. ^ Noh, Ji Yun; Jeong, Hye Won; Kim, Jerome H.; Shin, Eui-Cheol (November 5, 2021). "T cell-oriented strategies for controlling the COVID-19 pandemic". Nature Reviews. Immunology. 21 (11): 687–688. doi:10.1038/s41577-021-00625-9. PMC 8424399. PMID 34497383.
  20. ^ "2008 ~ 2023 | Laureates | Asan Award in Medicine | Asan Medical Center". asanawardinmedicine.amc.seoul.kr.
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