TY - JOUR
T1 - Immunosenescence, inflammaging, and cancer immunotherapy efficacy
AU - Rodriguez, Julieta E.
AU - Naigeon, Marie
AU - Goldschmidt, Vincent
AU - Roulleaux Dugage, Matthieu
AU - Seknazi, Lauren
AU - Danlos, Francois X.
AU - Champiat, Stephane
AU - Marabelle, Aurélien
AU - Michot, Jean Marie
AU - Massard, Christophe
AU - Besse, Benjamin
AU - Ferrara, Roberto
AU - Chaput, Nathalie
AU - Baldini, Capucine
N1 - Publisher Copyright:
© 2022 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022/1/1
Y1 - 2022/1/1
N2 - Introduction: Immunosenescence is a progressive remodeling of immune functions associated with a decreased ability of the immune system to set up an efficient immune response, both innate and adaptive, with an increase of highly differentiated T cells at the expense of naive T cells. The incidence and prevalence of most cancers increase with age, which can partly be explained by tumor escape mechanisms and decreased immunosurveillance. Aging is also associated with inflammaging, a low-grade proinflammatory state characterized by an increase in inflammatory mediators. Anti-cancer immunotherapy has profoundly changed the landscape of oncology therapy in the last 10 years. Modern T-cell targeted therapies such as bispecific T cell engagers, CAR-T cells, or immune checkpoint blockers may be theoretically affected by immunosenescence or inflammaging. Areas covered: A bibliographic review through PubMed and Embase was carried out using the following search terms: ‘immunosenescence,’ ‘immunotherapy,’ ‘inflammaging,’ ‘bispecific antibodies,’ ‘CAR-T cells,’ ‘immune checkpoint blockers,’ and ‘older patients.’ Expert opinion: This review explores the potential impact of immunosenescence and inflammaging on anti-cancer immunotherapy and therapeutic strategies that could counter immune senescence. A more dedicated research on immunosenescence biomarkers in future clinical trials is warranted for the development of new, more effective and safer therapies.
AB - Introduction: Immunosenescence is a progressive remodeling of immune functions associated with a decreased ability of the immune system to set up an efficient immune response, both innate and adaptive, with an increase of highly differentiated T cells at the expense of naive T cells. The incidence and prevalence of most cancers increase with age, which can partly be explained by tumor escape mechanisms and decreased immunosurveillance. Aging is also associated with inflammaging, a low-grade proinflammatory state characterized by an increase in inflammatory mediators. Anti-cancer immunotherapy has profoundly changed the landscape of oncology therapy in the last 10 years. Modern T-cell targeted therapies such as bispecific T cell engagers, CAR-T cells, or immune checkpoint blockers may be theoretically affected by immunosenescence or inflammaging. Areas covered: A bibliographic review through PubMed and Embase was carried out using the following search terms: ‘immunosenescence,’ ‘immunotherapy,’ ‘inflammaging,’ ‘bispecific antibodies,’ ‘CAR-T cells,’ ‘immune checkpoint blockers,’ and ‘older patients.’ Expert opinion: This review explores the potential impact of immunosenescence and inflammaging on anti-cancer immunotherapy and therapeutic strategies that could counter immune senescence. A more dedicated research on immunosenescence biomarkers in future clinical trials is warranted for the development of new, more effective and safer therapies.
KW - CART cells
KW - Immunosenescence
KW - bispecific T-cell engagers
KW - immune checkpoint inhibitors
KW - inflammaging
KW - older patients
UR - http://www.scopus.com/inward/record.url?scp=85134168907&partnerID=8YFLogxK
U2 - 10.1080/14737140.2022.2098718
DO - 10.1080/14737140.2022.2098718
M3 - Article
C2 - 35815381
AN - SCOPUS:85134168907
SN - 1473-7140
VL - 22
SP - 915
EP - 926
JO - Expert Review of Anticancer Therapy
JF - Expert Review of Anticancer Therapy
IS - 9
ER -