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LTX-315 (Oncopore™)

A short synthetic anticancer peptide and novel immunotherapeutic agent

, &
Article: e29181 | Received 07 May 2014, Accepted 09 May 2014, Published online: 25 Jun 2014

Figures & data

Figure 1. LTX-315 is a synthetic cationic peptide with anticancer properties. Intralesional administration of LTX-315 induces cellular lysis (necrosis) through membrane destabilization, leading to a cascade of events that stimulate the immune system. Intracellular content consisting of DAMPs such as ATP and HMGB1, together with tumor antigens, are released into the tumor microenvironment. This induces an inflammatory response and the subsequent production of local inflammatory cytokines, which will initiate the maturation and recruitment of DCs into the tumor bed. Activated DCs are then primed for antigen engulfment and antigen presentation to T cells, creating tumor-specific cytotoxic CD8+ T lymphocytes capable of eradicating residual cancer cells. ATP, adenosine triphosphate; DAMPs, danger-associated molecular pattern molecules; DC, dendritic cell; CTLs, cytotoxic CD8+ T lymphocytes; HMGB1, high mobility group box protein 1; TME, tumor microenvironment;.

Figure 1. LTX-315 is a synthetic cationic peptide with anticancer properties. Intralesional administration of LTX-315 induces cellular lysis (necrosis) through membrane destabilization, leading to a cascade of events that stimulate the immune system. Intracellular content consisting of DAMPs such as ATP and HMGB1, together with tumor antigens, are released into the tumor microenvironment. This induces an inflammatory response and the subsequent production of local inflammatory cytokines, which will initiate the maturation and recruitment of DCs into the tumor bed. Activated DCs are then primed for antigen engulfment and antigen presentation to T cells, creating tumor-specific cytotoxic CD8+ T lymphocytes capable of eradicating residual cancer cells. ATP, adenosine triphosphate; DAMPs, danger-associated molecular pattern molecules; DC, dendritic cell; CTLs, cytotoxic CD8+ T lymphocytes; HMGB1, high mobility group box protein 1; TME, tumor microenvironment;.

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