RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      KCI등재 SCOPUS

      Effectiveness of Mavrilimumab in Viral Infections Including SARS-CoV-2 Infection - A Brief Review

      한글로보기

      https://www.riss.kr/link?id=A107337440

      • 0

        상세조회
      • 0

        다운로드
      서지정보 열기
      • 내보내기
      • 내책장담기
      • 공유하기
      • 오류접수

      부가정보

      다국어 초록 (Multilingual Abstract)

      Hyperinflammation and cytokine storm has been noted as a poor prognostic factor in patients with severe pneumonia related to coronavirus disease 2019 (COVID-19). In COVID-19, pathogenic myeloid cell overactivation is found to be a vital mediator of damage to tissues, hypercoagulability, and the cytokine storm. These cytokines unselectively infiltrate various tissues, such as the lungs and heart, and nervous system. This cytokine storm can hence cause multi-organ dysfunction and life-threatening complications. Mavrilimumab is a monoclonal antibody (mAb) that may be helpful in some cases with COVID-19. During an inflammation, Granulocyte-macrophage colony-stimulating factor (GM-CSF) release is crucial to driving both innate and adaptive immune responses. The GM-CSF immune response is triggered when an antigen attaches to the host cell and induces the signaling pathway. Mavrilimumab antagonizes the action of GM-CSF and decreases the hyperinflammation associated with pneumonia in COVID-19, therefore strengthening the rationale that mavrilimumab when added to the standard protocol of treatment could improve the clinical outcomes in COVID-19 patients, specifically those patients with pneumonia. With this review paper, we aim to demonstrate the inhibitory effect of mavrilimumab on cytokine storms in patients with COVID-19 by reviewing published clinical trials and emphasize the importance of extensive future trials.
      번역하기

      Hyperinflammation and cytokine storm has been noted as a poor prognostic factor in patients with severe pneumonia related to coronavirus disease 2019 (COVID-19). In COVID-19, pathogenic myeloid cell overactivation is found to be a vital mediator of da...

      Hyperinflammation and cytokine storm has been noted as a poor prognostic factor in patients with severe pneumonia related to coronavirus disease 2019 (COVID-19). In COVID-19, pathogenic myeloid cell overactivation is found to be a vital mediator of damage to tissues, hypercoagulability, and the cytokine storm. These cytokines unselectively infiltrate various tissues, such as the lungs and heart, and nervous system. This cytokine storm can hence cause multi-organ dysfunction and life-threatening complications. Mavrilimumab is a monoclonal antibody (mAb) that may be helpful in some cases with COVID-19. During an inflammation, Granulocyte-macrophage colony-stimulating factor (GM-CSF) release is crucial to driving both innate and adaptive immune responses. The GM-CSF immune response is triggered when an antigen attaches to the host cell and induces the signaling pathway. Mavrilimumab antagonizes the action of GM-CSF and decreases the hyperinflammation associated with pneumonia in COVID-19, therefore strengthening the rationale that mavrilimumab when added to the standard protocol of treatment could improve the clinical outcomes in COVID-19 patients, specifically those patients with pneumonia. With this review paper, we aim to demonstrate the inhibitory effect of mavrilimumab on cytokine storms in patients with COVID-19 by reviewing published clinical trials and emphasize the importance of extensive future trials.

      더보기

      참고문헌 (Reference)

      1 Griffin JD, "The biology of GM-CSF:regulation of production and interaction with its receptor" 8 (8): 35-44, 1990

      2 Broughton SE, "The GM-CSF/IL-3/IL-5 cytokine receptor family: from ligand recognition to initiation of signaling" 250 : 277-302, 2012

      3 Bonaventura A, "Targeting GM-CSF in COVID-19 Pneumonia: Rationale and Strategies" 1 : 1625-, 2020

      4 U.S. National Library of Medicine, "Study of Mavrilimumab (KPL-301) in participants hopistalized with severe corona virus disease 2019 (COVID-19) pneumonia and hyper-inflammation"

      5 Costela-Ruiz VJ, "SARS-CoV-2infection: The role of cytokines in COVID-19 disease" 54 : 62-75, 2020

      6 Hoffmann M, "SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor" 181 : 271-280, 2020

      7 Singh Tomar PP, "SARS-CoV-2 E protein is a potential ion channel that can be inhibited by Gliclazide and Memantine" 530 : 10-14, 2020

      8 Wu C, "Risk factors associated with acute respiratory distress syndrome and death in patients with coronavirus disease 2019pneumonia in Wuhan, China" 180 : 934-943, 2020

      9 Trapnell BC, "Pulmonary alveolar proteinosis, a primary immunodeficiency of impaired GM-CSF stimulation of macrophages" 21 : 514-521, 2009

      10 Zhou Y, "Pathogenic T cells and inflammatory monocytes incite inflammatory storm in severe COVID-19 patients" 2020

      1 Griffin JD, "The biology of GM-CSF:regulation of production and interaction with its receptor" 8 (8): 35-44, 1990

      2 Broughton SE, "The GM-CSF/IL-3/IL-5 cytokine receptor family: from ligand recognition to initiation of signaling" 250 : 277-302, 2012

      3 Bonaventura A, "Targeting GM-CSF in COVID-19 Pneumonia: Rationale and Strategies" 1 : 1625-, 2020

      4 U.S. National Library of Medicine, "Study of Mavrilimumab (KPL-301) in participants hopistalized with severe corona virus disease 2019 (COVID-19) pneumonia and hyper-inflammation"

      5 Costela-Ruiz VJ, "SARS-CoV-2infection: The role of cytokines in COVID-19 disease" 54 : 62-75, 2020

      6 Hoffmann M, "SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor" 181 : 271-280, 2020

      7 Singh Tomar PP, "SARS-CoV-2 E protein is a potential ion channel that can be inhibited by Gliclazide and Memantine" 530 : 10-14, 2020

      8 Wu C, "Risk factors associated with acute respiratory distress syndrome and death in patients with coronavirus disease 2019pneumonia in Wuhan, China" 180 : 934-943, 2020

      9 Trapnell BC, "Pulmonary alveolar proteinosis, a primary immunodeficiency of impaired GM-CSF stimulation of macrophages" 21 : 514-521, 2009

      10 Zhou Y, "Pathogenic T cells and inflammatory monocytes incite inflammatory storm in severe COVID-19 patients" 2020

      11 McClure BJ, "Molecular assembly of the ternary granulocyte-macrophage colony-stimulating factor receptor complex" 101 : 1308-1315, 2003

      12 Di Franco M, "Mavrilimumab: an evidence based review of its potential in the treatment of rheumatoid arthritis" 9 : 2014

      13 Crotti C, "Mavrilimumab: a unique insight and update on the current status in the treatment of rheumatoid arthritis" 28 : 573-581, 2019

      14 . Burmester GR, "Mavrilimumab, a human monoclonal antibody targeting GM-CSF receptor-α, in subjects with rheumatoid arthritis: a randomised, doubleblind, placebo-controlled, phase I, first-in-human study" 70 : 1542-1549, 2011

      15 Burmester GR, "Mavrilimumab, a fully human granulocyte-macrophage colony-stimulating factor receptor α monoclonal antibody: long-term safety and efficacy in patients with rheumatoid arthritis" 70 : 679-678, 2018

      16 U.S. National Library of Medicine, "Mavrilimumab to reduce progression of acute respiratory failure in COVID-19 pneumonia and systemic hyper-inflmation. NCT04492514"

      17 U.S. National Library of Medicine, "Mavrilimumab to reduce progression of acute respiratory failure in COVID-19 pneumonia and systemic hyper-inflammation. NCT04463004"

      18 U.S National Library of Medicine, "Mavrilimumab in severe COVID-19 pneumonia and hyper-inflammation (COMBAT-19)"

      19 Nicholls JM, "Lung pathology of fatal severe acute respiratory syndrome" 361 : 1773-1778, 2003

      20 Cardone M, "Lessons learned to date on COVID-19 hyperinflammatory syndrome: considerations for interventions to mitigate SARS-CoV-2 viral infection and detrimental hyperinflammation" 11 : 1131-, 2020

      21 Cavalli G, "Interleukin-1 blockade with highdose anakinra in patients with COVID-19, acute respiratory distress syndrome, and hyperinflammation: a retrospective cohort study" 2 : e325-e331, 2020

      22 Lang FM, "GM-CSF-based treatments in COVID-19:reconciling opposing therapeutic approaches" 20 : 507-514, 2020

      23 Hamilton JA, "GM-CSF in inflammation and autoimmunity" 23 : 403-408, 2002

      24 De Luca G, "GM-CSF blockade with mavrilimumab in severe COVID-19 pneumonia and systemic hyperinflammation: a single-centre, prospective cohort study" 2 : e465-e473, 2020

      25 Hamilton JA, "GM-CSF as a target in inflammatory/autoimmune disease: current evidence and future therapeutic potential" 11 : 457-465, 2015

      26 Takeuchi T, "Efficacy and safety of mavrilimumab in Japanese subjects with rheumatoid arthritis: findings from a Phase IIa study" 2 : 21-30, 2015

      27 Cheng LL, "Effect of Recombinant Human Granulocyte Colony-Stimulating Factor for Patients With Coronavirus Disease 2019 (COVID-19) and Lymphopenia: A Randomized Clinical Trial" 181 : 71-78, 2021

      28 Bhattacharya P, "Dual Role of GM-CSF as a pro-inflammatory and a regulatory cytokine: implications for immune therapy" 35 : 585-599, 2015

      29 Ramani T, "Cytokines: the good, the bad, and the deadly" 34 : 355-365, 2015

      30 Huang C, "Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China" 395 : 497-506, 2020

      31 Siddiqi HK, "COVID-19 illness in native and immunosuppressed states: A clinical-therapeutic staging proposal" 39 : 405-407, 2020

      32 Lisi L, "Approaching coronavirus disease 2019: Mechanisms of action of repurposed drugs with potential activity against SARS-CoV-2" 180 : 114169-, 2020

      33 Weinblatt ME, "A Randomized Phase IIb Study of Mavrilimumab and Golimumab in Rheumatoid Arthritis" 70 : 49-59, 2018

      더보기

      분석정보

      View

      상세정보조회

      0

      Usage

      원문다운로드

      0

      대출신청

      0

      복사신청

      0

      EDDS신청

      0

      동일 주제 내 활용도 TOP

      더보기

      주제

      연도별 연구동향

      연도별 활용동향

      연관논문

      연구자 네트워크맵

      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

      인용정보 인용지수 설명보기

      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2010-02-25 학술지명변경 한글명 : 감염과화학요법 -> Infection and Chemotherapy
      외국어명 : Infection and Chemotherapy -> 미등록
      KCI등재후보
      2010-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2009-08-25 학술지명변경 외국어명 : 미등록 -> Infection and Chemotherapy KCI등재후보
      2008-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      2008-01-01 평가 등재후보 탈락 (등재후보1차)
      2006-01-01 평가 등재후보 1차 FAIL (등재후보2차) KCI등재후보
      2005-05-27 학술지등록 한글명 : 감염과화학요법
      외국어명 : 미등록
      KCI등재후보
      2005-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2004-01-01 평가 등재후보 1차 FAIL (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      더보기

      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.24 0.24 0.24
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.2 0.2 0.46 0.29
      더보기

      이 자료와 함께 이용한 RISS 자료

      나만을 위한 추천자료

      해외이동버튼