AIH Therapy: Beyond First-Line
Purpose of Review The purpose of the article is to review treatment options for patients with AIH for whom first-line therapy is not successful. We outline recommended approaches for providers and new therapies on the horizon. Recent Findings Budesonide, while advantageous in some respects, may not...
Ausführliche Beschreibung
Autor*in: |
Adao, Irina [verfasserIn] Klepper, Arielle [verfasserIn] Tana, Michele [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2024 |
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Schlagwörter: |
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Anmerkung: |
© The Author(s) 2024 |
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Übergeordnetes Werk: |
Enthalten in: Current transplantation reports - Springer US, 2002, 23(2024), 3 vom: 08. März, Seite 341-348 |
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Übergeordnetes Werk: |
volume:23 ; year:2024 ; number:3 ; day:08 ; month:03 ; pages:341-348 |
Links: |
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DOI / URN: |
10.1007/s11901-024-00657-4 |
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SPR056869592 |
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10.1007/s11901-024-00657-4 doi (DE-627)SPR056869592 (SPR)s11901-024-00657-4-e DE-627 ger DE-627 rakwb eng 610 VZ Adao, Irina verfasserin aut AIH Therapy: Beyond First-Line 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2024 Purpose of Review The purpose of the article is to review treatment options for patients with AIH for whom first-line therapy is not successful. We outline recommended approaches for providers and new therapies on the horizon. Recent Findings Budesonide, while advantageous in some respects, may not be as effective as predniso(lo)ne. Mycophenolate mofetil is most effective in the setting of azathioprine intolerance and less effective when the response to azathioprine has been inadequate. Infliximab is the biologic agent with the most evidence for use in AIH. Clinical trials studying interleukin 2, regulatory T cells, inhibitors of BAFF signaling, and immunoproteasome inhibitors have been initiated but more research is needed, particularly in Black people, Indigenous people, and People of Color. Summary While multiple agents have been reported as second- or third-line therapies, the evidence is limited. Future research will require multicenter collaboration and should explore therapeutics supported by molecular studies. Autoimmune hepatitis (dpeaa)DE-He213 Second-line therapy (dpeaa)DE-He213 Third-line therapy (dpeaa)DE-He213 AIH treatment (dpeaa)DE-He213 Klepper, Arielle verfasserin aut Tana, Michele verfasserin aut Enthalten in Current transplantation reports Springer US, 2002 23(2024), 3 vom: 08. März, Seite 341-348 Online-Ressource (DE-627)787023302 (DE-600)2772824-9 (DE-576)407570381 2195-9595 nnns volume:23 year:2024 number:3 day:08 month:03 pages:341-348 https://dx.doi.org/10.1007/s11901-024-00657-4 X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER AR 23 2024 3 08 03 341-348 |
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10.1007/s11901-024-00657-4 doi (DE-627)SPR056869592 (SPR)s11901-024-00657-4-e DE-627 ger DE-627 rakwb eng 610 VZ Adao, Irina verfasserin aut AIH Therapy: Beyond First-Line 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2024 Purpose of Review The purpose of the article is to review treatment options for patients with AIH for whom first-line therapy is not successful. We outline recommended approaches for providers and new therapies on the horizon. Recent Findings Budesonide, while advantageous in some respects, may not be as effective as predniso(lo)ne. Mycophenolate mofetil is most effective in the setting of azathioprine intolerance and less effective when the response to azathioprine has been inadequate. Infliximab is the biologic agent with the most evidence for use in AIH. Clinical trials studying interleukin 2, regulatory T cells, inhibitors of BAFF signaling, and immunoproteasome inhibitors have been initiated but more research is needed, particularly in Black people, Indigenous people, and People of Color. Summary While multiple agents have been reported as second- or third-line therapies, the evidence is limited. Future research will require multicenter collaboration and should explore therapeutics supported by molecular studies. Autoimmune hepatitis (dpeaa)DE-He213 Second-line therapy (dpeaa)DE-He213 Third-line therapy (dpeaa)DE-He213 AIH treatment (dpeaa)DE-He213 Klepper, Arielle verfasserin aut Tana, Michele verfasserin aut Enthalten in Current transplantation reports Springer US, 2002 23(2024), 3 vom: 08. März, Seite 341-348 Online-Ressource (DE-627)787023302 (DE-600)2772824-9 (DE-576)407570381 2195-9595 nnns volume:23 year:2024 number:3 day:08 month:03 pages:341-348 https://dx.doi.org/10.1007/s11901-024-00657-4 X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER AR 23 2024 3 08 03 341-348 |
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10.1007/s11901-024-00657-4 doi (DE-627)SPR056869592 (SPR)s11901-024-00657-4-e DE-627 ger DE-627 rakwb eng 610 VZ Adao, Irina verfasserin aut AIH Therapy: Beyond First-Line 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2024 Purpose of Review The purpose of the article is to review treatment options for patients with AIH for whom first-line therapy is not successful. We outline recommended approaches for providers and new therapies on the horizon. Recent Findings Budesonide, while advantageous in some respects, may not be as effective as predniso(lo)ne. Mycophenolate mofetil is most effective in the setting of azathioprine intolerance and less effective when the response to azathioprine has been inadequate. Infliximab is the biologic agent with the most evidence for use in AIH. Clinical trials studying interleukin 2, regulatory T cells, inhibitors of BAFF signaling, and immunoproteasome inhibitors have been initiated but more research is needed, particularly in Black people, Indigenous people, and People of Color. Summary While multiple agents have been reported as second- or third-line therapies, the evidence is limited. Future research will require multicenter collaboration and should explore therapeutics supported by molecular studies. Autoimmune hepatitis (dpeaa)DE-He213 Second-line therapy (dpeaa)DE-He213 Third-line therapy (dpeaa)DE-He213 AIH treatment (dpeaa)DE-He213 Klepper, Arielle verfasserin aut Tana, Michele verfasserin aut Enthalten in Current transplantation reports Springer US, 2002 23(2024), 3 vom: 08. März, Seite 341-348 Online-Ressource (DE-627)787023302 (DE-600)2772824-9 (DE-576)407570381 2195-9595 nnns volume:23 year:2024 number:3 day:08 month:03 pages:341-348 https://dx.doi.org/10.1007/s11901-024-00657-4 X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER AR 23 2024 3 08 03 341-348 |
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10.1007/s11901-024-00657-4 doi (DE-627)SPR056869592 (SPR)s11901-024-00657-4-e DE-627 ger DE-627 rakwb eng 610 VZ Adao, Irina verfasserin aut AIH Therapy: Beyond First-Line 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2024 Purpose of Review The purpose of the article is to review treatment options for patients with AIH for whom first-line therapy is not successful. We outline recommended approaches for providers and new therapies on the horizon. Recent Findings Budesonide, while advantageous in some respects, may not be as effective as predniso(lo)ne. Mycophenolate mofetil is most effective in the setting of azathioprine intolerance and less effective when the response to azathioprine has been inadequate. Infliximab is the biologic agent with the most evidence for use in AIH. Clinical trials studying interleukin 2, regulatory T cells, inhibitors of BAFF signaling, and immunoproteasome inhibitors have been initiated but more research is needed, particularly in Black people, Indigenous people, and People of Color. Summary While multiple agents have been reported as second- or third-line therapies, the evidence is limited. Future research will require multicenter collaboration and should explore therapeutics supported by molecular studies. Autoimmune hepatitis (dpeaa)DE-He213 Second-line therapy (dpeaa)DE-He213 Third-line therapy (dpeaa)DE-He213 AIH treatment (dpeaa)DE-He213 Klepper, Arielle verfasserin aut Tana, Michele verfasserin aut Enthalten in Current transplantation reports Springer US, 2002 23(2024), 3 vom: 08. März, Seite 341-348 Online-Ressource (DE-627)787023302 (DE-600)2772824-9 (DE-576)407570381 2195-9595 nnns volume:23 year:2024 number:3 day:08 month:03 pages:341-348 https://dx.doi.org/10.1007/s11901-024-00657-4 X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER AR 23 2024 3 08 03 341-348 |
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10.1007/s11901-024-00657-4 doi (DE-627)SPR056869592 (SPR)s11901-024-00657-4-e DE-627 ger DE-627 rakwb eng 610 VZ Adao, Irina verfasserin aut AIH Therapy: Beyond First-Line 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2024 Purpose of Review The purpose of the article is to review treatment options for patients with AIH for whom first-line therapy is not successful. We outline recommended approaches for providers and new therapies on the horizon. Recent Findings Budesonide, while advantageous in some respects, may not be as effective as predniso(lo)ne. Mycophenolate mofetil is most effective in the setting of azathioprine intolerance and less effective when the response to azathioprine has been inadequate. Infliximab is the biologic agent with the most evidence for use in AIH. Clinical trials studying interleukin 2, regulatory T cells, inhibitors of BAFF signaling, and immunoproteasome inhibitors have been initiated but more research is needed, particularly in Black people, Indigenous people, and People of Color. Summary While multiple agents have been reported as second- or third-line therapies, the evidence is limited. Future research will require multicenter collaboration and should explore therapeutics supported by molecular studies. Autoimmune hepatitis (dpeaa)DE-He213 Second-line therapy (dpeaa)DE-He213 Third-line therapy (dpeaa)DE-He213 AIH treatment (dpeaa)DE-He213 Klepper, Arielle verfasserin aut Tana, Michele verfasserin aut Enthalten in Current transplantation reports Springer US, 2002 23(2024), 3 vom: 08. März, Seite 341-348 Online-Ressource (DE-627)787023302 (DE-600)2772824-9 (DE-576)407570381 2195-9595 nnns volume:23 year:2024 number:3 day:08 month:03 pages:341-348 https://dx.doi.org/10.1007/s11901-024-00657-4 X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER AR 23 2024 3 08 03 341-348 |
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Purpose of Review The purpose of the article is to review treatment options for patients with AIH for whom first-line therapy is not successful. We outline recommended approaches for providers and new therapies on the horizon. Recent Findings Budesonide, while advantageous in some respects, may not be as effective as predniso(lo)ne. Mycophenolate mofetil is most effective in the setting of azathioprine intolerance and less effective when the response to azathioprine has been inadequate. Infliximab is the biologic agent with the most evidence for use in AIH. Clinical trials studying interleukin 2, regulatory T cells, inhibitors of BAFF signaling, and immunoproteasome inhibitors have been initiated but more research is needed, particularly in Black people, Indigenous people, and People of Color. Summary While multiple agents have been reported as second- or third-line therapies, the evidence is limited. Future research will require multicenter collaboration and should explore therapeutics supported by molecular studies. © The Author(s) 2024 |
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Purpose of Review The purpose of the article is to review treatment options for patients with AIH for whom first-line therapy is not successful. We outline recommended approaches for providers and new therapies on the horizon. Recent Findings Budesonide, while advantageous in some respects, may not be as effective as predniso(lo)ne. Mycophenolate mofetil is most effective in the setting of azathioprine intolerance and less effective when the response to azathioprine has been inadequate. Infliximab is the biologic agent with the most evidence for use in AIH. Clinical trials studying interleukin 2, regulatory T cells, inhibitors of BAFF signaling, and immunoproteasome inhibitors have been initiated but more research is needed, particularly in Black people, Indigenous people, and People of Color. Summary While multiple agents have been reported as second- or third-line therapies, the evidence is limited. Future research will require multicenter collaboration and should explore therapeutics supported by molecular studies. © The Author(s) 2024 |
abstract_unstemmed |
Purpose of Review The purpose of the article is to review treatment options for patients with AIH for whom first-line therapy is not successful. We outline recommended approaches for providers and new therapies on the horizon. Recent Findings Budesonide, while advantageous in some respects, may not be as effective as predniso(lo)ne. Mycophenolate mofetil is most effective in the setting of azathioprine intolerance and less effective when the response to azathioprine has been inadequate. Infliximab is the biologic agent with the most evidence for use in AIH. Clinical trials studying interleukin 2, regulatory T cells, inhibitors of BAFF signaling, and immunoproteasome inhibitors have been initiated but more research is needed, particularly in Black people, Indigenous people, and People of Color. Summary While multiple agents have been reported as second- or third-line therapies, the evidence is limited. Future research will require multicenter collaboration and should explore therapeutics supported by molecular studies. © The Author(s) 2024 |
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We outline recommended approaches for providers and new therapies on the horizon. Recent Findings Budesonide, while advantageous in some respects, may not be as effective as predniso(lo)ne. Mycophenolate mofetil is most effective in the setting of azathioprine intolerance and less effective when the response to azathioprine has been inadequate. Infliximab is the biologic agent with the most evidence for use in AIH. Clinical trials studying interleukin 2, regulatory T cells, inhibitors of BAFF signaling, and immunoproteasome inhibitors have been initiated but more research is needed, particularly in Black people, Indigenous people, and People of Color. Summary While multiple agents have been reported as second- or third-line therapies, the evidence is limited. 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