Table 1.
The Effects of Tamoxifen on Immunity
Model / patient population | Key observations |
---|---|
Studies in humans | |
Breast cancer patients treated with tamoxifen | ↓ Natural Killer cell activity [19, 20] |
↑ proliferation of lymphocytes in presence of mitogen [19] | |
↓ number of CD4 lymphocytes [20] | |
Case reports of a patient with Riedel’s disease | Tamoxifen induced remission [21] |
Case report of a patient with dermatomyositis rash | Tamoxifen induced remission [22] |
In vivo animal models | |
Mice models that develop autoimmune diseases akin to systemic lupus erythematosus mice |
Delayed onset of disease [24] |
↑ survival of tamoxifen treated mice [23, 25, 26] | |
↓ proteinuria [23, 24, 25] | |
↓ auto-antibody production [23, 25] | |
↓ thrombocytopaenia [23, 24] | |
Normal leukocyte count [24] | |
↓ number of splenic B-cells [25] | |
↓ serum tumor necrosis alpha levels [25] | |
↓ lymphadenopathy [26] | |
↓ renal disease on histopathological examination [23, 24, 25] | |
Murine autoimmune encephalitis | ↓ disease symptoms [27] |
↓ degree of demyelination [27] | |
↓ myelin-induced T-cell production [27] | |
↓ ability of dendritic cells to stimulate myelin-specific T-cells [27] | |
Differential effects on Th1 and Th2 cells with Th2 bias [27] | |
Autoimmune uveitis in rats | Delayed onset of disease [28] |
Differential effects on Th1 and Th2 cells with Th2 bias [28] | |
In vivo models | |
Human peripheral blood lymphocytes | ↓ alloantigen-induced T-cell proliferation [15] |
↓ cytokine production [15] | |
Human monocyte-derived dendritic cells | Distinct phenotype (CD14−, CD1a−, CD80−, CD86+) [29] |
↓ capacity to induce proliferation amongst allogeneic T-cells [29] | |
↓ production of interleukin 12 upon stimulation [29] | |
Human synovial fluid macrophages | Distinct phenotype (CD14−, CD1a−, CD80−, CD86+) [30] |
↓ capacity to induce proliferation amongst allogeneic T-cells [30] |
Symbols ↑ = increase; ↓ = decrease.