Immunogenic cell stress and death

被引:0
|
作者
Guido Kroemer
Claudia Galassi
Laurence Zitvogel
Lorenzo Galluzzi
机构
[1] Equipe labellisée par la Ligue contre le cancer,
[2] Centre de Recherche des Cordeliers,undefined
[3] INSERM U1138,undefined
[4] Sorbonne Université,undefined
[5] Université de Paris,undefined
[6] Institut Universitaire de France,undefined
[7] Metabolomics and Cell Biology Platforms,undefined
[8] Gustave Roussy Cancer Center,undefined
[9] Pôle de Biologie,undefined
[10] Hôpital Européen Georges Pompidou,undefined
[11] AP-HP,undefined
[12] Department of Radiation Oncology,undefined
[13] Weill Cornell Medical College,undefined
[14] Gustave Roussy Comprehensive Cancer Institute,undefined
[15] Université Paris Saclay,undefined
[16] Faculty of Medicine,undefined
[17] INSERM U1015,undefined
[18] Equipe labellisée par la Ligue contre le cancer,undefined
[19] Center of Clinical Investigations in Biotherapies of Cancer (CICBT) BIOTHERIS,undefined
[20] Sandra and Edward Meyer Cancer Center,undefined
[21] Caryl and Israel Englander Institute for Precision Medicine,undefined
来源
Nature Immunology | 2022年 / 23卷
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摘要
Dying mammalian cells emit numerous signals that interact with the host to dictate the immunological correlates of cellular stress and death. In the absence of reactive antigenic determinants (which is generally the case for healthy cells), such signals may drive inflammation but cannot engage adaptive immunity. Conversely, when cells exhibit sufficient antigenicity, as in the case of infected or malignant cells, their death can culminate with adaptive immune responses that are executed by cytotoxic T lymphocytes and elicit immunological memory. Suggesting a key role for immunogenic cell death (ICD) in immunosurveillance, both pathogens and cancer cells evolved strategies to prevent the recognition of cell death as immunogenic. Intriguingly, normal cells succumbing to conditions that promote the formation of post-translational neoantigens (for example, oxidative stress) can also drive at least some degree of antigen-specific immunity, pointing to a novel implication of ICD in the etiology of non-infectious, non-malignant disorders linked to autoreactivity.
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页码:487 / 500
页数:13
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