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. 2016 Aug 25;107(9):1193–1197. doi: 10.1111/cas.12986

Table 1.

LAG‐3 and cancer

Year Disease Finding References
1999 Cancer sLAG‐3 could be a vaccine since it could active antigen presenting cells (APC). 41
2001 Cancer sLAG‐3 could improve interactions between in situ T cells and DC, and potentiate Th1‐type response to target tumors, and, thus, could be a cancer vaccine. 40
2003 Breast cancer Therapy involving LAG‐3 relative could block the progression of mammary carcinogenesis in an animal model. 42
2005 Cancer LAG‐3 related anti‐cancer therapy was effective and shared a similar mechanism with IL‐12 27
2006 Cancer (melanoma or colorectal cancer) Human LAG‐3 Ig induced specific CD8+ T‐cell activity. The activation of this protein is a potential adjuvant treatment for cancer vaccines 56
2006 Cancer sLAG‐3, used as a cancer vaccine, bound MHC class II+ APC, induced DC maturation and was well tolerated 57
2006 Hodgkin's lymphoma (HL) LAG‐3 played important roles in the suppression of EBV immunity in HL 58
2010 Ovarian cancer Inhibiting both LAG‐3 and PD‐1 pathways could efficiently improve T‐cell function 59
2010 Chronic lymphocytic leukemia (CLL) High LAG‐3 expression indicated poor treatment outcomes in CLL 60
2010 Cancer LAG‐3 defined Tregs were more numerous in tumor sites 61
2010 Multiple myeloma LAG‐3 gene single nucleotide polymorphism (SNP) increased susceptibility to multiple myeloma 62
2011 Melanoma LAG‐3/MHC class II interaction in MHC class II‐positive melanoma tumors might serve as a bidirectional immune escape pathway shared by tumor cells and immune cells and renews the interest in MHC class II phenotyping for more efficient therapeutic strategies 63
2012 Cancer LAG‐3/Pdcd1 mice lived markedly longer than wild type and could eliminate multiple transplantable tumors 20
2012 Hepatocellular carcinoma (HCC) Increased LAG‐3 expression was observed in TIL in HCC 64
2014 Melanoma LAG‐3 activated pDC were found in tumor areas, which could suppress the immune environment 65
2015 Gastric cancer In gastric cancer, expression of PD‐1 and LAG‐3 on CD4+ and CD8+ T cells was elevated and might impair cell‐mediated immunity after surgery 66

DC, dendritic cells; LAG‐3, lymphocyte‐activation gene‐3; sLAG‐3, soluble LAG‐3; TIL, tumor‐infiltrating lymphocytes.