“…Among the biological mechanisms involved in anticancer immunity, T-cell adaptive immunity has been suggested to play a key role in this setting [ 56 ]; more specifically, CD8+ T cells, CD4+ T helper cells, FOXP3+ regulatory T cells, memory T cells, and NK cells can infiltrate the stromal tissue, thus modifying the host immune response against cancer cells [ 57 , 58 ]. Over the last decade, several reports have highlighted that the GC microenvironment could be associated with the infiltration of tumor lymphocytes [ 5 , 59 ]. TILs may cause potent anticancer responses, preventing tumor growth and eradicating cancer cells; moreover, TILs have been suggested to enhance inflammation through the secretion of chemokines, cytokines, and matrix metalloproteinases [ 60 , 61 ].…”