Induction and Anti-Tumor Function of Tertiary Lymphoid Organs

CHEN Hong, HU Xiang, ZHANG Hui-yuan, HU Hong-bo

Abstract

To induce the development of tertiary lymphoid organs (TLO) in a mouse model of melanoma and to evaluate TLO’s functions in antitumor immunity.  Methods  Lymphotoxin-beta receptor (LTβR) was overexpressed in NIH3T3 cells through the lentivirus system and the overexpression efficiency of LTβR in LTβR-NIH3T3 cells was examined. Western blot and qPCR were used to examine the non-canonical nuclear factor (NF)-κB signaling pathway in NIH3T3 cells overexpressing LTβR. B16-OVA melanoma mouse model was constructed to explore the induction of TLO and anti-tumor functions of TLO in LTβR-NIH3T3 cells.  Results  LTβR was overexpressed in NIH3T3 cells through the lentivirus system, and flow cytometry showed that the proportion of GFP+ cells reached 99%. The overexpression of LTβR activated the non-canonical NF-κB signaling pathway in NIH3T3 cells. Findings from the mouse tumor model suggest that the injection of LTβR-NIH3T3 cells successfully induced the development of lymphoid tissue around the tumor and enhanced the tumor infiltration of T cells and MHCⅡ+ macrophages, significantly inhibiting tumor growth and prolonging the survival of tumor-bearing mice.  Conclusion  LTβR-NIH3T3 cells promoted anti-tumor immunity by inducing TLO development, which may provide new perspectives for tumor immunotherapy.

 

Keywords: Tertiary lymphoid organs, Anti-tumor immunity, Non-canonical NF-κB signaling pathway

 

Full Text:

PDF


References


DIEU-NOSJEAN M C, GIRALDO N A, KAPLON H, et al. Tertiary lymphoid structures, drivers of the anti-tumor responses in human cancers. Immunol Rev,2016,271(1): 260–275.

SAUTES-FRIDMAN C, LAWAND M, GIRALDO N A, et al. Tertiary lymphoid structures in cancers: Prognostic value, regulation, and manipulation for therapeutic intervention. Front Immunol, 2016, 7: 407[2021-08-11]. https://doi.org/10.3389/fimmu.2016.00407.

DOMBLIDES C, ROCHEFORT J, RIFFARD C, et al. Tumor-associated tertiary lymphoid structures: from basic and clinical knowledge to therapeutic manipulation. Front Immunol, 2021, 12: 698604[2021-09-14]. https://doi.org/10.3389/fimmu.2021.698604.

GAGO DA GRACA C, VAN BAARSEN L G M, MEBIUS R E. Tertiary lymphoid structures: Diversity in their development, composition, and role. J Immunol,2021,206(2): 273–281.

SUN S C. The non-canonical NF-kappaB pathway in immunity and inflammation. Nat Rev Immunol,2017,17(9): 545–558.

TANG H, ZHU M, QIAO J, et al. Lymphotoxin signalling in tertiary lymphoid structures and immunotherapy. Cell Mol Immunol,2017, 14(10): 809–818.

KRISHNAMURTY A T, TURLEY S J. Lymph node stromal cells: Cartographers of the immune system. Nat Immunol,2020,21(4): 369–380.

DENTON A E, INNOCENTIN S, CARR E J, et al. Type I interferon induces CXCL13 to support ectopic germinal center formation. J Exp Med,2019,216(3): 621–637.

SAUTES-FRIDMAN C, PETITPREZ F, CALDERARO J, et al. Tertiary lymphoid structures in the era of cancer immunotherapy. Nat Rev Cancer,2019,19(6): 307–325.

LUO R, CHENG Y, CHANG D, et al. Tertiary lymphoid organs are associated with the progression of kidney damage and regulated by interleukin-17A. Theranostics,2021,11(1): 117–131.

NERVIANI A, PITZALIS C. Role of chemokines in ectopic lymphoid structures formation in autoimmunity and cancer. J Leukoc Biol,2018, 104(2): 333–341.

RODRIGUEZ A B, ENGELHARD V H. Insights into tumor-associated tertiary lymphoid structures: Novel targets for antitumor immunity and cancer immunotherapy. Cancer Immunol Res,2020,8(11): 1338–1345.

WIRSING A M, ERVIK I K, SEPPOLA M, et al. Presence of high-endothelial venules correlates with a favorable immune microenvironment in oral squamous cell carcinoma. Mod Pathol,2018, 31(6): 910–922.

SAVAS P, SALGADO R, DENKERT C, et al. Clinical relevance of host immunity in breast cancer: From TILs to the clinic. Nat Rev Clin Oncol, 2016,13(4): 228–241.

POSCH F, SILINA K, LEIBL S, et al. Maturation of tertiary lymphoid structures and recurrence of stage Ⅱ and Ⅲ colorectal cancer. Oncoimmunology, 2018, 7(2): e1378844[2021-09-12].https://doi.org/10.1080/2162402X.2017.1378844.

CABRITA R, LAUSS M, SANNA A, et al. Tertiary lymphoid structures improve immunotherapy and survival in melanoma. Nature,2020, 577(7791): 561–565.

JOHANSSON-PERCIVAL A, HE B, LI Z J, et al. De novo induction of intratumoral lymphoid structures and vessel normalization enhances immunotherapy in resistant tumors. Nat Immunol,2017,18(11): 1207–1217.

WEIDEN J, TEL J, FIGDOR C G. Synthetic immune niches for cancer immunotherapy. Nat Rev Immunol,2018,18(3): 212–219.

WEINSTEIN A M, CHEN L, BRZANA E A, et al. Tbet and IL-36gamma cooperate in therapeutic DC-mediated promotion of ectopic lymphoid organogenesis in the tumor microenvironment. Oncoimmunology, 2017, 6(6): e1322238[2021-09-17]. https://doi. org/10.1080/2162402X.2017.1322238.

ZHU G, FALAHAT R, WANG K, et al. Tumor-associated tertiary lymphoid structures: Gene-expression profiling and their bioengineering. Front Immunol, 2017, 8: 767[2021-07-15]. https://doi.org/10.3389/fimmu.2017.00767.

ZHU G, NEMOTO S, MAILLOUX A W, et al. Induction of tertiary lymphoid structures with antitumor function by a lymph node-derived stromal cell line. Front Immunol, 2018, 9: 1609[2021-08-24]. https://doi.org/10.3389/fimmu.2018.01609.

ANDO M, ITO M, SRIRAT T, et al. Memory T cell, exhaustion, and tumor immunity. Immunol Med,2020,43(1): 1–9.

FARHOOD B, NAJAFI M, MORTEZAEE K. CD8+ cytotoxic T lymphocytes in cancer immunotherapy: A review. J Cell Physiol,2019, 234(6): 8509–8521.

LIN Z, HUANG L, LI S, et al. Pan-cancer analysis of genomic properties and clinical outcome associated with tumor tertiary lymphoid structure. Sci Rep,2020,10(1): 21530.


Refbacks

  • There are currently no refbacks.