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Hormesis in cancer immunology

Does the quantity of an immune reactant matter?

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Article: e29312 | Received 20 May 2014, Accepted 21 May 2014, Published online: 25 Jun 2014

Figures & data

Figure 1. The immune response curve to antibody-based anticancer therapeutics. Very low levels of tumor-directed antibody (Zone A) have no effect on tumor growth, but as this dose increases (red zone B-D) tumor growth is stimulated via activation of PI3K/AKT pathway, and high infiltration of M2 polarized macrophages. There is a dose of antibody that generates a maximum stimulatory effect (Zone C). Increasing the dose of antibody finally leads to tumor growth inhibition (Zone E to F) via natural killer (NK) cell mediated antibody-dependent complement cascade (ADCC) and complement-mediated tumor cell lysis. However, this curve goes through a null zone, suggesting there is a dose of antibody that generates stimulatory and inhibitory mechanisms in quantities that mutually cancel each other out to give no net overall effect on tumor growth.

Figure 1. The immune response curve to antibody-based anticancer therapeutics. Very low levels of tumor-directed antibody (Zone A) have no effect on tumor growth, but as this dose increases (red zone B-D) tumor growth is stimulated via activation of PI3K/AKT pathway, and high infiltration of M2 polarized macrophages. There is a dose of antibody that generates a maximum stimulatory effect (Zone C). Increasing the dose of antibody finally leads to tumor growth inhibition (Zone E to F) via natural killer (NK) cell mediated antibody-dependent complement cascade (ADCC) and complement-mediated tumor cell lysis. However, this curve goes through a null zone, suggesting there is a dose of antibody that generates stimulatory and inhibitory mechanisms in quantities that mutually cancel each other out to give no net overall effect on tumor growth.

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