PANoptosis is a prominent unique, innate immune, inflammatory, and lytic cell death pathway initiated by innate immune sensors and driven by caspases and RIPKs through multiprotein PANoptosome complexes. ^{[1] [2]} The assembly of the PANoptosome cell death complex occurs in response to germline-encoded pattern-recognition receptors (PRRs) sensing pathogens, including bacterial, viral, and fungal infections, as well as pathogen-associated molecular patterns, damage-associated molecular patterns, and cytokines that are released during infections, inflammatory conditions, and cancer. ^{[3] [4] [5] [6] [7] [8] [9] [10] [11] [12] [13] [14] [15] [16] [1]} Several PANoptosome complexes, such as the ZBP1-, AIM2-, RIPK1-, NLRC5- and NLRP12-PANoptosomes, have been characterized so far. ^{[1] [17] [18] [19] [20] [21] [22] [23]}

Emerging genetic, molecular, and biochemical studies have identified extensive crosstalk among the molecular components across various cell death pathways in response to a variety of pathogens and innate immune triggers. ^{[3] [4]} Historically, inflammatory caspase-mediated pyroptosis  and RIPK-driven necroptosis were described as two major inflammatory cell death pathways. While the PANoptosis pathway has some molecular components in common with pyroptosis and necroptosis, as well as with the non-lytic apoptosis pathway, these mechanisms are separate processes that are associated with distinct triggers, protein complexes, and execution pathways. ^[2] Inflammasome-dependent pyroptosis involves inflammatory caspases, including caspase-1 and caspase-11 in mice, and caspases-1, -4, and - 5 in humans, and is executed by gasdermin D. ^{[24] [25] [26] [27] [28] [29] [30]} In contrast, necroptosis occurs via RIPK1/3-mediated MLKL activation, which is downstream of caspase-8 inhibition. ^{[31] [32] [33] [34]} On the other hand, PANoptosis is [TDK1] driven by caspases and RIPKs and is executed by gasdermins, MLKL, and potentially other yet to be identified molecules cleaved by caspases. ^{[35] [36] [37] [38] [39] [40] [19] [21]} Moreover, caspase-8 is essential for cell death in PANoptosis ^{[41] [42]} but needs to be inactivated or inhibited to induce necroptosis. ^{[43] [44]}

PANoptosis has now been identified in a variety of infections, including viral ( influenza A virus, herpes simplex virus 1 (HSV1), coronavirus), bacterial ( Yersinia pseudotuberculosis, Francisella novicida), and fungal ( Candida albicans, Aspergillus fumigatus). PANoptosis has also been implicated in inflammatory diseases, neurological diseases, and cancer. ^{[45] [46] [47] [48] [49] [50] [51] [52] [53] [54]} Activation of PANoptosis can clear infected cells for host defense, and it has shown preclinical promise as an anti-cancer strategy. For example, PANoptosis is important for host defense during influenza infection through the ZBP1-PANoptosome and during Francisella and HSV1 infections through the AIM2-PANoptosome. ^{[5] [7] [17] [19]} Additionally, treatment of cancer cells with the PANoptosis-inducing agents TNF and IFN-γ ^{[55] [6]} can reduce tumor size in preclinical models. ^[56] The combination of the nuclear export inhibitor selinexor and IFN can also cause PANoptosis and regress tumors in preclinical models. ^{[3] [57]} However, excess activation of PANoptosis can be associated with inflammation, inflammatory disease, and cytokine storm syndromes. ^{[6] [11] [58] [21] [1]} Treatments that block TNF and IFN-γ to prevent PANoptosis have provided therapeutic benefit in preclinical models of cytokine storm syndromes, including cytokine shock, SARS-CoV-2 infection, sepsis, and hemophagocytic lymphohistiocytosis, suggesting the therapeutic potential of modulating this pathway. ^{[6] [59]} Further studies with beta-coronaviruses have shown that IFN can induce ZBP1-mediated PANoptosis during SARS-CoV-2 infection, thereby limiting the efficacy of IFN treatment during infection and resulting in morbidity and mortality. This suggests that inhibiting ZBP1 may improve the therapeutic efficacy of IFN therapy during SARS-CoV-2 infection and possibly other inflammatory conditions where IFN-mediated cell death and pathology occur. ^{[60] [61]} More recent evidence suggests that NLRP12-mediated PANoptosis is activated by heme, which can be released by red blood cell lysis during infection or inflammatory disease, in combination with specific components of infection or cellular damage.  Deletion of NLRP12 protects against pathology in animal models of hemolytic disease, suggesting this could also act as a therapeutic target. Similarly, the NLRC5-PANoptosome, which also contains NLRP12, was identified as a response to NAD+ depletion downstream of heme-containing triggers. Deletion of NLRC5 protects against not only hemolytic disease models, but also colitis and HLH models. ^{[22] [23]} Additionally, PANoptosis can also be induced by heat stress (HS), such as fever, during infection, and NINJ1 is a known key executioner in this context. Deletion of NINJ1 in a murine model of HS and infection reduces mortality; furthermore, deleting essential PANoptosis effectors upstream completely rescues the mice from mortality, thereby identifying NINJ1 and PANoptosis effectors as potential therapeutic targets. ^[62]

The regulation of PANoptosis involves numerous PANoptosomes, which encompass multiple sensor molecules such as NLRP3, ZBP1, AIM2, and NLRP12, along with complex-forming molecules such as caspases and RIPKs. These components activate various downstream cell death executioners and play a role in disease. Therefore, modulating the components of this pathway has potential for therapy.

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