Psoriasis 2012
DOI: 10.5772/26413
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Biotech on the Rise: The Treatment of Psoriasis with Biological Drugs

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“…Some approaches for increasing the number of effector T cells at the tumor site are based on the delivery of mAbs to activate surface costimulatory T cell receptors, such as B7, 4-1BB or OX40, which promote the expansion and increase the antitumor immune response of CD8 + T cells (Table 9). [329,330] In one report, the treatment of mice bearing B16F10 melanoma tumors with PEGylated liposomes decorated with the Ab 4-1BB (also known as CD137) and the same liposomes with an engineered fusion protein of IL-2 and a fragment crystallizable region of an antibody (IL-2Fc) anchored, led to a positive antitumor efficacy, with decreased systemic toxicity in comparison to the free drugs. [331] In another case, the same melanoma murine model was used to test the efficacy of PLGA NPs conjugated to anti-PD-1 and OX40 mAbs.…”
Section: Mabs To Induce the Antitumor Activity Of Immune Cellsmentioning
confidence: 99%
“…Some approaches for increasing the number of effector T cells at the tumor site are based on the delivery of mAbs to activate surface costimulatory T cell receptors, such as B7, 4-1BB or OX40, which promote the expansion and increase the antitumor immune response of CD8 + T cells (Table 9). [329,330] In one report, the treatment of mice bearing B16F10 melanoma tumors with PEGylated liposomes decorated with the Ab 4-1BB (also known as CD137) and the same liposomes with an engineered fusion protein of IL-2 and a fragment crystallizable region of an antibody (IL-2Fc) anchored, led to a positive antitumor efficacy, with decreased systemic toxicity in comparison to the free drugs. [331] In another case, the same melanoma murine model was used to test the efficacy of PLGA NPs conjugated to anti-PD-1 and OX40 mAbs.…”
Section: Mabs To Induce the Antitumor Activity Of Immune Cellsmentioning
confidence: 99%