OncoImmunology (Jan 2020)

Helper T cell-dominant tertiary lymphoid structures are associated with disease relapse of advanced colorectal cancer

  • Kyoko Yamaguchi,
  • Mamoru Ito,
  • Hirofumi Ohmura,
  • Fumiyasu Hanamura,
  • Michitaka Nakano,
  • Kenji Tsuchihashi,
  • Shuntaro Nagai,
  • Hiroshi Ariyama,
  • Hitoshi Kusaba,
  • Hidetaka Yamamoto,
  • Yoshinao Oda,
  • Masafumi Nakamura,
  • Koichi Akashi,
  • Eishi Baba

DOI
https://doi.org/10.1080/2162402X.2020.1724763
Journal volume & issue
Vol. 9, no. 1

Abstract

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Tertiary lymphoid structures (TLSs), clusters of immune cells found around tumor tissue, have been shown to be associated with anti-tumor immunity, but the cellular composition within each TLS and whether the cellular composition of a TLS affects a patient’s prognosis are poorly understood. In the present study, each TLS was categorized according to its cellular composition determined by a system of multiplex immunohistochemical staining and quantitative analysis, and the correlation between the category and prognosis was examined. Sixty-seven patients with curatively resected stage II/III colorectal cancer (CRC) were enrolled. A TLS, consisting of germinal center B cells, follicular dendritic cells, T helper (Th) cells, B cells, cytotoxic T cells, and macrophages, was confirmed in the tumor tissue of 58 patients (87%). The densities of Th cells and macrophages were significantly higher in relapsed patients than in not-relapsed patients (p = .043 and p = .0076). A higher ratio of Th cells was the most significant independent risk factor for disease relapse on multivariate analysis. The subset increasing in Th cells was GATA3+ Th2. A total of 353 TLSs was divided into five clusters according to immune cell composition. Among them, the Th-rich type TLS was significantly increased (p = .0009) in relapsed patients. These data suggest the possibility that Th cell-dominant composition might disturb the anti-tumor immune response, and the function of each TLS might differ depending on its composition.

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