دورية أكاديمية

In situ vaccination with defined factors overcomes T cell exhaustion in distant tumors.

التفاصيل البيبلوغرافية
العنوان: In situ vaccination with defined factors overcomes T cell exhaustion in distant tumors.
المؤلفون: Khalil, Danny N.1,2,3,4, Suek, Nathan1, Campesato, Luis Felipe1, Budhu, Sadna1, Redmond, David1, Samstein, Robert M.5, Krishna, Chirag6, Panageas, Katherine S.7, Capanu, Marinela7, Houghton, Sean1, Hirschhorn, Daniel1, Zappasodi, Roberta1,2, Giese, Rachel1,8, Gasmi, Billel9, Schneider, Michael1, Gupta, Aditi1, Harding, James J.3,4, Moral, John Alec8, Balachandran, Vinod P.2,10, Wolchok, Jedd D.1,2,3,4 wolchokj@mskcc.org
المصدر: Journal of Clinical Investigation. Aug2019, Vol. 129 Issue 8, p3435-3447. 13p.
مصطلحات موضوعية: *T cells, *APOPTOSIS, *CELL tumors, *VACCINATION, *MELANOMA treatment, *PROTEINS, *RESEARCH, *IMMUNIZATION, *MELANOMA, *ANIMAL experimentation, *RESEARCH methodology, *CELL receptors, *EVALUATION research, *COMPARATIVE studies, *RESEARCH funding, *CANCER vaccines, *T-cell exhaustion, *ANTIGENS, *MICE, *CHEMICAL inhibitors
مستخلص: Irreversible T cell exhaustion limits the efficacy of programmed cell death 1 (PD-1) blockade. We observed that dual CD40-TLR4 stimulation within a single tumor restored PD-1 sensitivity and that this regimen triggered a systemic tumor-specific CD8+ T cell response. This approach effectively treated established tumors in diverse syngeneic cancer models, and the systemic effect was dependent on the injected tumor, indicating that treated tumors were converted into necessary components of this therapy. Strikingly, this approach was associated with the absence of exhausted PD-1hi T cells in treated and distant tumors, while sparing the intervening draining lymph node and spleen. Furthermore, patients with transcription changes like those induced by this therapy experienced improved progression-free survival with anti-PD-1 treatment. Dual CD40-TLR4 activation within a single tumor is thus an approach for overcoming resistance to PD-1 blockade that is unique in its ability to cause the loss of exhausted T cells within tumors while sparing nonmalignant tissues. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:00219738
DOI:10.1172/JCI128562