Targeting Innate Immune Cells for Immunotherapy

摘要

One of the most effective ways to modulate either positively or negatively host immune responses (i.e., to treat cancer and autoimmunity, resp.) is to target effector immune cells, such as B cells, CD4~(+), and CD8~(+) T cells, as well as professional antigen-presenting cells, such as dendritic cells (DCs), that promote the activation of the latter two. Frequently, this modulation is aimed at targeting the initiation of the T cell immune response, a process known as T cell priming, which affects not only T cell outcome but also B cell responses that are influenced by the help of CD4~(+) T cells. At present, several strategies include the optimization of adjuvants and drugs to manipulate the phenotype and function of DCs, frequently with their ex vivo drug treatment and their reintroduction into the host, activating/inhibiting ligands that interact with T cell activation, differentiation, and function. Another strategy consists in ex vivo T cell expansion and reinjection into the host, among others. Although these immunomodulating strategies have shown relatively high success in the clinic with promising therapeutic potential, there are many other strategies that target different immune cell types, especially those associated with the innate immune system, that play crucial roles in immunomodulation. Moreover, it has been evidenced during recent years that cells of the innate immune system can modulate and dictate the inflammatory environment that will take place during T cell priming. Cells of the innate immune system are key players not only at initiating and regulating adaptive immune responses, such as those elicited against pathogens and cancer, but also at modulating tolerance to autoantigens to prevent autoimmune diseases. While some of these cells are considered exclusively innate, as natural killer (NK) cells and innate lymphoid cells (ILCs), others are positioned at the interface of innate and adaptive immune responses, such as DCs, macrophages, monocytes, and natural killer T (NKT) cells. The role of these cells in different immune responses has led to the design of targeted immunotherapies aimed at controlling diseases, such as cancer, autoimmunity, and allergy, as well as potentiating immune responses against pathogens. In this special issue, original studies and review articles are encompassed together to highlight recent discoveries on immunotherapy involving innate immune cells to combat cancer and pathogens.In the area of cancer immunotherapy, R. Yi et al. analyze how innate immune cell-based immunotherapy combined with classical therapies can improve the outcome of castration-resistant prostate cancer. They perform a meta-analysis aimed at studying the efficacy of the immunotherapeutic vaccine sipuleucel-T combined with regular treatments directed to the androgen receptor (AR). Sipuleucel-T is a cellular immunotherapy which consists in autologous peripheral blood mononuclear cells (PBMCs) incubated with recombinant specific prostatic antigens fused with granulocyte-macrophage colony-stimulating factor. They described that this immunotherapy greatly improved the efficacy of the traditional therapy. Also aiming at cancer, P. G. Lokhov and E. E. Balashova investigate the efficacy of targeting tumor vasculature antigens and their efficacy against cancer growth. They describe the novel composition called SANTAVAC (Set of All Natural Target Antigens for Vaccination Against Cancer) and their use against tumoral microvasculature. Finally, I. Knippertz et al. used a combined promoter system of adenoviral vectors in order to induce maturation changes in DCs. By targeting the active expression of heat shock factor (mHSF), they induced maturation of human DCs, with a concomitant increase in the expression of proinflammatory cytokines and costimulatory molecules. This approach, combined with specific antigens, could be useful not only in cancer immunotherapy but also in improving immunity against pathogens.