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      Verification with the utility of an established rapid assessment of brain safety for newly developed vaccines

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      https://www.riss.kr/link?id=A106504552

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      In the twenty-first century, high contagious infectious diseases such as SARS (Severe Acute Respiratory Syndrome), MERS (Middle East Respiratory Syndrome), FMD (Foot-and-Mouth Disease) and AI (Avian Influenza) have become very prevalent, causing treat harm to humans and animals in aspect of public health, and economical issues. The critical problem is that newly-reported infectious diseases that humans firstly experience are expected to continue to emerge, and these diseases will be spreading out rapidly. Therefore, rapid and safe supplies of effective vaccines are most pivotal to prevent the rapid prevalent of new infection, but international standards or assessing protocol the safety of urgent vaccines are not established well. In our previous study, since we established a module to assess the brain safety of urgent vaccines, therefore, it is necessary to verify that this established module for assessing brain safety could work effectively in commercially available two vaccines (one killed- and on live-vaccines). We compared the results of Evans blue (EB) assay and qPCR analysis by injection of two kinds of vaccines, PBS and Lipopolysaccharide (LPS) under the condition of the module previously reported. We confirmed that the brain safety test module for urgent vaccine we established is very reproducible. Therefore, it is believed that this vaccine safety testing method can be used to validate brain safety when prompt supply of a newly developed vaccines is needed.
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      In the twenty-first century, high contagious infectious diseases such as SARS (Severe Acute Respiratory Syndrome), MERS (Middle East Respiratory Syndrome), FMD (Foot-and-Mouth Disease) and AI (Avian Influenza) have become very prevalent, causing treat...

      In the twenty-first century, high contagious infectious diseases such as SARS (Severe Acute Respiratory Syndrome), MERS (Middle East Respiratory Syndrome), FMD (Foot-and-Mouth Disease) and AI (Avian Influenza) have become very prevalent, causing treat harm to humans and animals in aspect of public health, and economical issues. The critical problem is that newly-reported infectious diseases that humans firstly experience are expected to continue to emerge, and these diseases will be spreading out rapidly. Therefore, rapid and safe supplies of effective vaccines are most pivotal to prevent the rapid prevalent of new infection, but international standards or assessing protocol the safety of urgent vaccines are not established well. In our previous study, since we established a module to assess the brain safety of urgent vaccines, therefore, it is necessary to verify that this established module for assessing brain safety could work effectively in commercially available two vaccines (one killed- and on live-vaccines). We compared the results of Evans blue (EB) assay and qPCR analysis by injection of two kinds of vaccines, PBS and Lipopolysaccharide (LPS) under the condition of the module previously reported. We confirmed that the brain safety test module for urgent vaccine we established is very reproducible. Therefore, it is believed that this vaccine safety testing method can be used to validate brain safety when prompt supply of a newly developed vaccines is needed.

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      참고문헌 (Reference)

      1 Tomohiro Kondo, "Transient forebrain ischemia induces impairment in cognitive performance prior to extensive neuronal cell death in Mongolian gerbil (Meriones unguiculatus)" 대한수의학회 19 (19): 505-511, 2018

      2 이순신, "Time-dependent changes of calbindin D-28K and parvalbumin immunoreactivity in the hippocampus of rats with streptozotocin-induced type 1 diabetes" 대한수의학회 14 (14): 373-380, 2013

      3 Cereijido M, "Tight junction and polarity interaction in the transporting epithelial phenotype" 1778 (1778): 770-793, 2008

      4 Fanning AS, "The tight junction protein ZO-1 establishes a link between the transmembrane protein occludin and the actin cytoskeleton" 273 (273): 29745-29753, 1998

      5 Edelblum KL, "The tight junction in inflammatory disease : communication breakdown" 9 (9): 715-720, 2009

      6 Elia L, "The knockout of miR-143 and-145 alters smooth muscle cell maintenance and vascular homeostasis in mice : correlates with human disease" 16 (16): 1590-1598, 2009

      7 Ballabh P, "The blood-brain barrier : an overview : structure, regulation, and clinical implications" 16 (16): 1-13, 2004

      8 Cummins PM, "Occludin : one protein, many forms" 32 (32): 242-250, 2012

      9 Waterson MJ, "Neuronal regulation of energy homeostasis : beyond the hypothalamus and feeding" 22 (22): 962-970, 2015

      10 Jin Hee Kim, "Neonatal influenza virus infection affects myelination in influenza-recovered mouse brain" 대한수의학회 19 (19): 750-758, 2018

      1 Tomohiro Kondo, "Transient forebrain ischemia induces impairment in cognitive performance prior to extensive neuronal cell death in Mongolian gerbil (Meriones unguiculatus)" 대한수의학회 19 (19): 505-511, 2018

      2 이순신, "Time-dependent changes of calbindin D-28K and parvalbumin immunoreactivity in the hippocampus of rats with streptozotocin-induced type 1 diabetes" 대한수의학회 14 (14): 373-380, 2013

      3 Cereijido M, "Tight junction and polarity interaction in the transporting epithelial phenotype" 1778 (1778): 770-793, 2008

      4 Fanning AS, "The tight junction protein ZO-1 establishes a link between the transmembrane protein occludin and the actin cytoskeleton" 273 (273): 29745-29753, 1998

      5 Edelblum KL, "The tight junction in inflammatory disease : communication breakdown" 9 (9): 715-720, 2009

      6 Elia L, "The knockout of miR-143 and-145 alters smooth muscle cell maintenance and vascular homeostasis in mice : correlates with human disease" 16 (16): 1590-1598, 2009

      7 Ballabh P, "The blood-brain barrier : an overview : structure, regulation, and clinical implications" 16 (16): 1-13, 2004

      8 Cummins PM, "Occludin : one protein, many forms" 32 (32): 242-250, 2012

      9 Waterson MJ, "Neuronal regulation of energy homeostasis : beyond the hypothalamus and feeding" 22 (22): 962-970, 2015

      10 Jin Hee Kim, "Neonatal influenza virus infection affects myelination in influenza-recovered mouse brain" 대한수의학회 19 (19): 750-758, 2018

      11 Huber JD, "Molecular physiology and pathophysiology of tight junctions in the blood-brain barrier" 24 (24): 719-725, 2001

      12 Banks WA, "Lipopolysaccharideinduced blood-brain barrier disruption : roles of cyclooxygenase, oxidative stress, neuroinflammation, and elements of the neurovascular unit" 12 : 223-, 2015

      13 Jangula A, "Lipopolysaccharide-induced blood brain barrier permeability is enhanced by alpha-synuclein expression" 551 : 23-27, 2013

      14 Qin LH, "LPS Induces Occludin Dysregulation in Cerebral Microvascular Endothelial Cells via MAPK Signaling and Augmenting MMP-2 Levels" 2015 : 120641-, 2015

      15 Vigh B, "Its supposed role in the nonsynaptic signal transmission of the brain" 19 (19): 607-628, 2004

      16 Kitler ME, "Influenza and the work of the World Health Organization" 20 (20): S5-S14, 2002

      17 Barreto ML, "Infectious diseases epidemiology" 60 (60): 192-195, 2006

      18 Fu BM, "Experimental methods and transport models for drug delivery across the blood-brain barrier" 13 (13): 1346-1359, 2012

      19 백혜경, "Establishment of minimal positive-control conditions to ensure brain safety during rapid development of emergency vaccines" 대한수의학회 18 : 371-379, 2017

      20 Yi SS, "Enhanced expressions of arginine vasopressin(Avp)in the hypothalamic paraventricular and supraoptic nuclei of type 2 diabetic rats" 33 (33): 833-841, 2008

      21 Gunzel D, "Claudins and the modulation of tight junction permeability" 93 (93): 525-569, 2013

      22 Stamatovic SM, "Brain endothelial cell-cell junctions : how to"open"the blood brain barrier" 6 (6): 179-192, 2008

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2026 평가예정 재인증평가 신청대상 (재인증)
      2020-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2017-01-01 평가 등재학술지 유지 (계속평가) KCI등재
      2013-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2006-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2005-07-03 학술지명변경 한글명 : Korean Association For Laboratory Animal Science -> Laboratory Animal Research
      외국어명 : Korean Association For Laboratory Animal Science -> Laboratory Animal Research
      KCI등재후보
      2004-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.16 0.16 0.16
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.25 0.19 0.415 0.03
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