MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1158/2767-9764.crc-22-0050

Медицинская библиотека · Cancer research communications · 2022

Mixed Response to Cancer Immunotherapy is Driven by Intratumor Heterogeneity and Differential Interlesion Immune Infiltration.

Morinaga Takao, Inozume Takashi, Kawazu Masahito, Ueda Youki, Sax Nicolas, Yamashita Kazuo, Kawashima Shusuke, Nagasaki Joji, Ueno Toshihide, Lin Jason, Ohara Yuuki, Kuwata Takeshi, Yukami Hiroki, Kawazoe Akihito, Shitara Kohei, Honobe-Tabuchi Akiko, Ohnuma Takehiro, Kawamura Tatsuyoshi, Umeda Yoshiyasu, Kawahara Yu, Nakamura Yasuhiro, Kiniwa Yukiko, Morita Ayako, Ichihara Eiki, Kiura Katsuyuki, Enokida Tomohiro, Tahara Makoto, Hasegawa Yoshinori, Mano Hiroyuki, Suzuki Yutaka, Nishikawa Hiroyoshi, Togashi Yosuke

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

UNLABELLED: Some patients experience mixed response to immunotherapy, whose biological mechanisms and clinical impact have been obscure. We obtained two tumor samples from lymph node (LN) metastatic lesions in a same patient. Whole exome sequencing for the both tumors and single-cell sequencing for the both tumor-infiltrating lymphocytes (TIL) demonstrated a significant difference in tumor clonality and TILs' characteristics, especially exhausted T-cell clonotypes, although a close relationship between the tumor cell and T-cell clones were observed as a response of an overlapped exhausted T-cell clone to an overlapped neoantigen. To mimic the clinical setting, we generated a mouse model of several clones from a same tumor cell line. Similarly, differential tumor clones harbored distinct TILs, and one responded to programmed cell death protein 1 (PD-1) blockade but the other did not in this model. We further conducted cohort study (n = 503) treated with PD-1 blockade monotherapies to investigate the outcome of mixed response. Patients with mixed responses to PD-1 blockade had a poor prognosis in our cohort. Particularly, there were significant differences in both tumor and T-cell clones between the primary and LN lesions in a patient who experienced tumor response to anti-PD-1 mAb followed by disease progression in only LN metastasis. Our results underscore that intertumoral heterogeneity alters characteristics of TILs even in the same patient, leading to mixed response to immunotherapy and significant difference in the outcome.

SIGNIFICANCE: Several patients experience mixed responses to immunotherapies, but the biological mechanisms and clinical significance remain unclear. Our results from clinical and mouse studies underscore that intertumoral heterogeneity alters characteristics of TILs even in the same patient, leading to mixed response to immunotherapy and significant difference in the outcome.

Для цитирования: Morinaga Takao, Inozume Takashi, Kawazu Masahito, Ueda Youki, Sax Nicolas, Yamashita Kazuo, Kawashima Shusuke, Nagasaki Joji, Ueno Toshihide, Lin Jason, Ohara Yuuki, Kuwata Takeshi, Yukami Hiroki, Kawazoe Akihito, Shitara Kohei, Honobe-Tabuchi Akiko, Ohnuma Takehiro, Kawamura Tatsuyoshi, Umeda Yoshiyasu, Kawahara Yu, Nakamura Yasuhiro, Kiniwa Yukiko, Morita Ayako, Ichihara Eiki, Kiura Katsuyuki, Enokida Tomohiro, Tahara Makoto, Hasegawa Yoshinori, Mano Hiroyuki, Suzuki Yutaka, Nishikawa Hiroyoshi, Togashi Yosuke. Mixed Response to Cancer Immunotherapy is Driven by Intratumor Heterogeneity and Differential Interlesion Immune Infiltration.. Cancer research communications. 2022. DOI: 10.1158/2767-9764.crc-22-0050.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.