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Identification of neoantigen-reactive T lymphocytes in the peripheral blood of a patient with glioblastoma

The adoptive transfer of naturally occurring T cells that recognize cancer neoantigens has led to durable tumor regressions in select patients with cancer. However, it remains unknown whether such T cells can be isolated from and used to treat patients with glioblastoma, a cancer that is refractory...

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Detalles Bibliográficos
Autores principales: Leko, Vid, Cafri, Gal, Yossef, Rami, Paria, Biman, Hill, Victoria, Gurusamy, Devikala, Zheng, Zhili, Gartner, Jared J, Prickett, Todd D, Goff, Stephanie L, Robbins, Paul, Lu, Yong-Chen, Rosenberg, Steven A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286793/
https://www.ncbi.nlm.nih.gov/pubmed/34266885
http://dx.doi.org/10.1136/jitc-2021-002882
Descripción
Sumario:The adoptive transfer of naturally occurring T cells that recognize cancer neoantigens has led to durable tumor regressions in select patients with cancer. However, it remains unknown whether such T cells can be isolated from and used to treat patients with glioblastoma, a cancer that is refractory to currently available therapies. To answer this question, we stimulated patient blood-derived memory T cells in vitro using peptides and minigenes that represented point mutations unique to patients’ tumors (ie, candidate neoantigens) and then tested their ability to specifically recognize these mutations. In a cohort of five patients with glioblastoma, we found that circulating CD4(+) memory T cells from one patient recognized a cancer neoantigen harboring a mutation in the EED gene (EED(H189N)) that was unique to that patient’s tumor. This finding suggests that neoantigen-reactive T cells could indeed be isolated from patients with glioblastoma, thereby providing a rationale for further efforts to develop neoantigen-directed adoptive T cell therapy for this disease.