Dae Chul Jeong

Dae Chul Jeong


Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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1 January 2021 in Journal of Korean Medical Science
Verified
Journal Article
Open access
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Hyun Mi KangHyun Mi Kang
Hyun Mi Kang
DJDae Chul Jeong
Dae Chul Jeong
BSByung-Kyu Suh
Byung-Kyu Suh
MAMoon Bae Ahn
Moon Bae Ahn
Kang HM, et al. J Korean Med Sci. 2020 Dec;36(3):e21. https://doi.org/10.3346/jkms.2021.36.e21

1 November 2004 in International Journal of Hematology
Verified
Journal Article
Closed access
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NCNak Gyun Chung
Nak Gyun Chung
DJDae Chul Jeong
Dae Chul Jeong
SPSoo Jeong Park
Soo Jeong Park
BCByung Ock Choi
Byung Ock Choi
BCBin Cho
Bin Cho
CHChi Wha Han
Chi Wha Han
Marrow stromal cells (MSC) produce a microenvironment supporting hematopoiesis and may contribute immune tolerance because of low immunogenicity and the suppressive effect of alloreactivity. We investigated whether cotransplantation of MSC could prevent lethal graft-versus-host disease (GVHD) in major histocompatibility complex mismatched allogeneic murine hematopoietic stem cell transplantation (HSCT) using female BALB/c (H-2d, recipient) and C3H/He (H-2k, donor) mice. MSC were obtained from C3H/He bone marrow cells (BMC). MSC and irradiated BALB/c splenocytes (SP) were cocultured with C3H/He SP or BMC. Nonirradiated MSC did not inhibit the proliferation of alloantigen-stimulated BMC and SP. However, irradiated MSC suppressed the proliferation of alloantigen-stimulated SP at a level comparable with that of immunosuppressive agents, and the suppression by MSC was reversed to a significant degree by interleukin 2. Lethally irradiated BALB/c mice received transplants of donor cells according to the following experimental groups (group A, BMC only; group B, BMC and SP; group C, BMC, SP, and MSC; group D, BMC and MSC). The survival rate in group D was higher than in the other groups (P =.0057), and the clinical GVHD scores and serum levels of interferon-γ were low in group D. Our results suggest that cotransplantation of MSC in HSCT prevents lethal GVHD, possibly by immune modulation.

13 October 2015 in BMC Infectious Diseases
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Journal Article
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SHSeung Beom Han
Seung Beom Han
SLSung Chul Lee
Sung Chul Lee
Soo-Young LeeSoo-Young Lee
Soo-Young Lee
DJDae Chul Jeong
Dae Chul Jeong
JKJin-Han Kang
Jin-Han Kang
The rate of urinary tract infections (UTIs) due to extended-spectrum β-lactamase (ESBL)-producing bacterial strains requiring carbapenem therapy has been increasing in children. This study was conducted to evaluate the effect of non-carbapenem antibiotic therapy on childhood UTIs caused by ESBL-producing Escherichia coli or Klebsiella pneumoniae. Medical records of children diagnosed with febrile UTIs due to E. coli or K. pneumoniae between 2010 and 2014 were retrospectively reviewed. The enrolled children were divided into two groups: the ESBL group and the non-ESBL group. Clinical characteristics and therapeutic responses were compared between the two groups. A total of 211 episodes of UTI (204 caused by E. coli; seven caused by K. pneumoniae) were identified in 205 children. Twenty-two (10.4 %) episodes were categorized into the ESBL group. There was no significant difference in the type of antibiotic administered between the two groups. No carbapenems were administered; however, aminoglycosides were administered for 79.1 % of the total episodes. Although empirical antibiotics were appropriate for more episodes in the non-ESBL group compared with the ESBL group (100.0 % vs. 90.9 %, p = 0.011), there were no significant differences in the frequency of defervescence, bacterial eradication from the urine, acute pyelonephritis and vesicoureteral reflux or fever duration between the two groups. Non-carbapenem antibiotics showed favourable therapeutic effects on childhood UTIs caused by ESBL-producing strains. Aminoglycosides can be an alternative to carbapenems in such cases.

1 January 2016 in Infection & Chemotherapy
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Journal Article
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JLJoon Hee Lee
Joon Hee Lee
SKSEULKI Kim
SEULKI Kim
SKSeong Koo Kim
Seong Koo Kim
SHSeung Beom Han
Seung Beom Han
JLJae Wook Saint Lee
Jae Wook Saint Lee
HKHack-Ki Kim
Hack-Ki Kim
Lee JH, et al. Infect Chemother. 2016 Sep;48(3):181-189. https://doi.org/10.3947/ic.2016.48.3.181

17 June 2013 in BMC Infectious Diseases
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Journal Article
Open access
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SHSeung Beom Han
Seung Beom Han
EBE Young Bae
E Young Bae
JLJae Wook Saint Lee
Jae Wook Saint Lee
DLDong-Gun Lee
Dong-Gun Lee
NCNack-Gyun Chung
Nack-Gyun Chung
HKHack-Ki Kim
Hack-Ki Kim
Background: This study was performed to compare the clinical characteristics and antibiotic susceptibilities of viridans streptococcal bacteremia (VSB) between febrile neutropenic adults and children with hematologic malignancies. Methods: The consecutive medical records of neutropenic patients with hematologic malignancies who were admitted to the Catholic Blood and Marrow Transplantation Center between April 2009 and July 2012, and who were subsequently diagnosed with VSB were reviewed retrospectively. A comparison was made between the clinical and laboratory characteristics of adults and pediatric patients and also between patients with cefepime susceptible or not susceptible VSB. Results: A total of 202 episodes (141 in adults, 61 in children) of VSB were identified. Among them, 26 (12.9%) cases had severe complications including four (2.0%) cases of death attributable to VSB. For antibacterial prophylaxis, most adults received ciprofloxacin (97.1%), but children more frequently received trimethoprim/sulfamethoxazole (86.9%). Oral mucositis (p = 0.005) and abdominal pain (p = 0.001) were found more frequently in adults, and cough was found more frequently in children (p = 0.004). The occurrence rates of severe complications and death attributable to VSB were not significantly different between adults and children. Susceptibility rate to cefepime was significantly higher in adults than children (85.7% vs. 66.1%, p = 0.002). However, in multivariate analysis, cefepime susceptibility had no impact on clinical outcome. Conclusions: There was no significant difference in clinical outcome between adults and children with VSB despite a difference in cefepime susceptibility. Hence, different antibiotic treatment strategies may not be necessary.

9 April 2014 in European Journal of Pediatrics
Verified
Journal Article
Closed access
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IYIn Hyuk Yoo
In Hyuk Yoo
HNHyunju Na
Hyunju Na
EBE. Young Bae
E. Young Bae
SHSeung Beom Han
Seung Beom Han
Soo-Young LeeSoo-Young Lee
Soo-Young Lee
JKJin-Han Kang
Jin-Han Kang