Soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies

Abstract Longitudinal sampling of tumor tissue from patients with solid cancers, aside from melanoma and a few other cases, is often unfeasible, and thus may not capture the plasticity of interactions between the tumor and immune system under selective pressure of a given therapy. Peripheral blood a...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Pitts, Stephanie C. [verfasserIn] Schlom, Jeffrey [verfasserIn] Donahue, Renee N. [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2024

Schlagwörter:	Peripheral immunome Blood analyses Soluble immune checkpoints Biomarkers Immune checkpoint inhibitors Conventional cancer therapies

Anmerkung:	© This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024

Übergeordnetes Werk:	Enthalten in: Journal of experimental & clinical cancer research - BioMed Central, 2008, 43(2024), 1 vom: 31. Mai
Übergeordnetes Werk:	volume:43 ; year:2024 ; number:1 ; day:31 ; month:05

Links:	Volltext

DOI / URN:	10.1186/s13046-024-03074-z

Katalog-ID:	SPR056076673

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spelling	10.1186/s13046-024-03074-z doi (DE-627)SPR056076673 (SPR)s13046-024-03074-z-e DE-627 ger DE-627 rakwb eng 610 VZ Pitts, Stephanie C. verfasserin (orcid)0000-0002-0103-3109 aut Soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024 Abstract Longitudinal sampling of tumor tissue from patients with solid cancers, aside from melanoma and a few other cases, is often unfeasible, and thus may not capture the plasticity of interactions between the tumor and immune system under selective pressure of a given therapy. Peripheral blood analyses provide salient information about the human peripheral immunome while offering technical and practical advantages over traditional tumor biopsies, and should be utilized where possible alongside interrogation of the tumor. Some common blood-based biomarkers used to study the immune response include immune cell subsets, circulating tumor DNA, and protein analytes such as cytokines. With the recent explosion of immune checkpoint inhibitors (ICI) as a modality of treatment in multiple cancer types, soluble immune checkpoints have become a relevant area of investigation for peripheral immune-based biomarkers. However, the exact functions of soluble immune checkpoints and their roles in cancer for the most part remain unclear. This review discusses current literature on the production, function, and expression of nine soluble immune checkpoints – sPD-L1, sPD-1, sCTLA4, sCD80, sTIM3, sLAG3, sB7-H3, sBTLA, and sHVEM – in patients with solid tumors, and explores their role as biomarkers of response to ICI as well as to conventional therapies (chemotherapy, radiotherapy, targeted therapy, and surgery) in cancer patients. Peripheral immunome (dpeaa)DE-He213 Blood analyses (dpeaa)DE-He213 Soluble immune checkpoints (dpeaa)DE-He213 Biomarkers (dpeaa)DE-He213 Immune checkpoint inhibitors (dpeaa)DE-He213 Conventional cancer therapies (dpeaa)DE-He213 Schlom, Jeffrey verfasserin (orcid)0000-0001-7932-4072 aut Donahue, Renee N. verfasserin (orcid)0000-0002-6828-3073 aut Enthalten in Journal of experimental & clinical cancer research BioMed Central, 2008 43(2024), 1 vom: 31. Mai (DE-627)568921380 (DE-600)2430698-8 1756-9966 nnns volume:43 year:2024 number:1 day:31 month:05 https://dx.doi.org/10.1186/s13046-024-03074-z X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 43 2024 1 31 05
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allfieldsGer	10.1186/s13046-024-03074-z doi (DE-627)SPR056076673 (SPR)s13046-024-03074-z-e DE-627 ger DE-627 rakwb eng 610 VZ Pitts, Stephanie C. verfasserin (orcid)0000-0002-0103-3109 aut Soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024 Abstract Longitudinal sampling of tumor tissue from patients with solid cancers, aside from melanoma and a few other cases, is often unfeasible, and thus may not capture the plasticity of interactions between the tumor and immune system under selective pressure of a given therapy. Peripheral blood analyses provide salient information about the human peripheral immunome while offering technical and practical advantages over traditional tumor biopsies, and should be utilized where possible alongside interrogation of the tumor. Some common blood-based biomarkers used to study the immune response include immune cell subsets, circulating tumor DNA, and protein analytes such as cytokines. With the recent explosion of immune checkpoint inhibitors (ICI) as a modality of treatment in multiple cancer types, soluble immune checkpoints have become a relevant area of investigation for peripheral immune-based biomarkers. However, the exact functions of soluble immune checkpoints and their roles in cancer for the most part remain unclear. This review discusses current literature on the production, function, and expression of nine soluble immune checkpoints – sPD-L1, sPD-1, sCTLA4, sCD80, sTIM3, sLAG3, sB7-H3, sBTLA, and sHVEM – in patients with solid tumors, and explores their role as biomarkers of response to ICI as well as to conventional therapies (chemotherapy, radiotherapy, targeted therapy, and surgery) in cancer patients. Peripheral immunome (dpeaa)DE-He213 Blood analyses (dpeaa)DE-He213 Soluble immune checkpoints (dpeaa)DE-He213 Biomarkers (dpeaa)DE-He213 Immune checkpoint inhibitors (dpeaa)DE-He213 Conventional cancer therapies (dpeaa)DE-He213 Schlom, Jeffrey verfasserin (orcid)0000-0001-7932-4072 aut Donahue, Renee N. verfasserin (orcid)0000-0002-6828-3073 aut Enthalten in Journal of experimental & clinical cancer research BioMed Central, 2008 43(2024), 1 vom: 31. Mai (DE-627)568921380 (DE-600)2430698-8 1756-9966 nnns volume:43 year:2024 number:1 day:31 month:05 https://dx.doi.org/10.1186/s13046-024-03074-z X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 43 2024 1 31 05
allfieldsSound	10.1186/s13046-024-03074-z doi (DE-627)SPR056076673 (SPR)s13046-024-03074-z-e DE-627 ger DE-627 rakwb eng 610 VZ Pitts, Stephanie C. verfasserin (orcid)0000-0002-0103-3109 aut Soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024 Abstract Longitudinal sampling of tumor tissue from patients with solid cancers, aside from melanoma and a few other cases, is often unfeasible, and thus may not capture the plasticity of interactions between the tumor and immune system under selective pressure of a given therapy. Peripheral blood analyses provide salient information about the human peripheral immunome while offering technical and practical advantages over traditional tumor biopsies, and should be utilized where possible alongside interrogation of the tumor. Some common blood-based biomarkers used to study the immune response include immune cell subsets, circulating tumor DNA, and protein analytes such as cytokines. With the recent explosion of immune checkpoint inhibitors (ICI) as a modality of treatment in multiple cancer types, soluble immune checkpoints have become a relevant area of investigation for peripheral immune-based biomarkers. However, the exact functions of soluble immune checkpoints and their roles in cancer for the most part remain unclear. This review discusses current literature on the production, function, and expression of nine soluble immune checkpoints – sPD-L1, sPD-1, sCTLA4, sCD80, sTIM3, sLAG3, sB7-H3, sBTLA, and sHVEM – in patients with solid tumors, and explores their role as biomarkers of response to ICI as well as to conventional therapies (chemotherapy, radiotherapy, targeted therapy, and surgery) in cancer patients. Peripheral immunome (dpeaa)DE-He213 Blood analyses (dpeaa)DE-He213 Soluble immune checkpoints (dpeaa)DE-He213 Biomarkers (dpeaa)DE-He213 Immune checkpoint inhibitors (dpeaa)DE-He213 Conventional cancer therapies (dpeaa)DE-He213 Schlom, Jeffrey verfasserin (orcid)0000-0001-7932-4072 aut Donahue, Renee N. verfasserin (orcid)0000-0002-6828-3073 aut Enthalten in Journal of experimental & clinical cancer research BioMed Central, 2008 43(2024), 1 vom: 31. Mai (DE-627)568921380 (DE-600)2430698-8 1756-9966 nnns volume:43 year:2024 number:1 day:31 month:05 https://dx.doi.org/10.1186/s13046-024-03074-z X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 43 2024 1 31 05
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author	Pitts, Stephanie C.
spellingShingle	Pitts, Stephanie C. ddc 610 misc Peripheral immunome misc Blood analyses misc Soluble immune checkpoints misc Biomarkers misc Immune checkpoint inhibitors misc Conventional cancer therapies Soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies
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topic_title	610 VZ Soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies Peripheral immunome (dpeaa)DE-He213 Blood analyses (dpeaa)DE-He213 Soluble immune checkpoints (dpeaa)DE-He213 Biomarkers (dpeaa)DE-He213 Immune checkpoint inhibitors (dpeaa)DE-He213 Conventional cancer therapies (dpeaa)DE-He213
topic	ddc 610 misc Peripheral immunome misc Blood analyses misc Soluble immune checkpoints misc Biomarkers misc Immune checkpoint inhibitors misc Conventional cancer therapies
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title	Soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies
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title_sort	soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies
title_auth	Soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies
abstract	Abstract Longitudinal sampling of tumor tissue from patients with solid cancers, aside from melanoma and a few other cases, is often unfeasible, and thus may not capture the plasticity of interactions between the tumor and immune system under selective pressure of a given therapy. Peripheral blood analyses provide salient information about the human peripheral immunome while offering technical and practical advantages over traditional tumor biopsies, and should be utilized where possible alongside interrogation of the tumor. Some common blood-based biomarkers used to study the immune response include immune cell subsets, circulating tumor DNA, and protein analytes such as cytokines. With the recent explosion of immune checkpoint inhibitors (ICI) as a modality of treatment in multiple cancer types, soluble immune checkpoints have become a relevant area of investigation for peripheral immune-based biomarkers. However, the exact functions of soluble immune checkpoints and their roles in cancer for the most part remain unclear. This review discusses current literature on the production, function, and expression of nine soluble immune checkpoints – sPD-L1, sPD-1, sCTLA4, sCD80, sTIM3, sLAG3, sB7-H3, sBTLA, and sHVEM – in patients with solid tumors, and explores their role as biomarkers of response to ICI as well as to conventional therapies (chemotherapy, radiotherapy, targeted therapy, and surgery) in cancer patients. © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024
abstractGer	Abstract Longitudinal sampling of tumor tissue from patients with solid cancers, aside from melanoma and a few other cases, is often unfeasible, and thus may not capture the plasticity of interactions between the tumor and immune system under selective pressure of a given therapy. Peripheral blood analyses provide salient information about the human peripheral immunome while offering technical and practical advantages over traditional tumor biopsies, and should be utilized where possible alongside interrogation of the tumor. Some common blood-based biomarkers used to study the immune response include immune cell subsets, circulating tumor DNA, and protein analytes such as cytokines. With the recent explosion of immune checkpoint inhibitors (ICI) as a modality of treatment in multiple cancer types, soluble immune checkpoints have become a relevant area of investigation for peripheral immune-based biomarkers. However, the exact functions of soluble immune checkpoints and their roles in cancer for the most part remain unclear. This review discusses current literature on the production, function, and expression of nine soluble immune checkpoints – sPD-L1, sPD-1, sCTLA4, sCD80, sTIM3, sLAG3, sB7-H3, sBTLA, and sHVEM – in patients with solid tumors, and explores their role as biomarkers of response to ICI as well as to conventional therapies (chemotherapy, radiotherapy, targeted therapy, and surgery) in cancer patients. © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024
abstract_unstemmed	Abstract Longitudinal sampling of tumor tissue from patients with solid cancers, aside from melanoma and a few other cases, is often unfeasible, and thus may not capture the plasticity of interactions between the tumor and immune system under selective pressure of a given therapy. Peripheral blood analyses provide salient information about the human peripheral immunome while offering technical and practical advantages over traditional tumor biopsies, and should be utilized where possible alongside interrogation of the tumor. Some common blood-based biomarkers used to study the immune response include immune cell subsets, circulating tumor DNA, and protein analytes such as cytokines. With the recent explosion of immune checkpoint inhibitors (ICI) as a modality of treatment in multiple cancer types, soluble immune checkpoints have become a relevant area of investigation for peripheral immune-based biomarkers. However, the exact functions of soluble immune checkpoints and their roles in cancer for the most part remain unclear. This review discusses current literature on the production, function, and expression of nine soluble immune checkpoints – sPD-L1, sPD-1, sCTLA4, sCD80, sTIM3, sLAG3, sB7-H3, sBTLA, and sHVEM – in patients with solid tumors, and explores their role as biomarkers of response to ICI as well as to conventional therapies (chemotherapy, radiotherapy, targeted therapy, and surgery) in cancer patients. © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024
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title_short	Soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies
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Peripheral blood analyses provide salient information about the human peripheral immunome while offering technical and practical advantages over traditional tumor biopsies, and should be utilized where possible alongside interrogation of the tumor. Some common blood-based biomarkers used to study the immune response include immune cell subsets, circulating tumor DNA, and protein analytes such as cytokines. With the recent explosion of immune checkpoint inhibitors (ICI) as a modality of treatment in multiple cancer types, soluble immune checkpoints have become a relevant area of investigation for peripheral immune-based biomarkers. However, the exact functions of soluble immune checkpoints and their roles in cancer for the most part remain unclear. 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Soluble immune checkpoints: implications for cancer prognosis and response to immune checkpoint therapy and conventional therapies

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