Therapeutic vaccines that have targeted established disease in cancer patients have not been successful in eliciting significant, long-lasting tumor regression.
Over the last several decades, most attempts to vaccinate against cancer and generate an antitumor response have been in patients with measurable tumors, and the clinical endpoint of such trials has been to evaluate a reduction in tumor burden.
The inability to effectively decrease tumor growth with active immunization is most likely due, in large part, to an unfavorable tumor microenvironment incapable of propagating a robust immune response.
The defects in the tumor environment are many.
The tumor itself can secrete a variety of substances that will depress or inhibit local immunity, such as IL-6 or TGF-β, which can stop the proliferation of antigen specific T cells.
Tumors can lose the expression of both MHC and costimulatory molecules, making them invincible to T cell attack.
The tumor microenvironment can also be adversely affected by the phenotype of local infiltrating T cells.
T cell subsets that limit the generation of tumor-specific immunity are abundant in cancer patients.
Investigations of preexistent tumor specific T cell immunity in patients with renal cell carcinoma have demonstrated that those patients living with disease were more likely to have tumor-specific Th2 responses, whereas those patients with no evidence of disease, i.e., successfully treated, were more likely to have Th1-specific immunity directed against renal cell cancer antigens.
Furthermore, CD25+ T regulatory cells are abundant in both the peripheral blood and tumors of patients with cancer.
These regulatory T cells have been shown to dampen the proliferation of cancer-specific cytotoxic T cells by direct contact with antigen-primed T cells and through elaboration of immunosuppressive cytokines such as TGF-β.
The active inhibition of a local inflammatory response by T cell subsets adds to the immune inhibitory cytokine milieu that characterizes most human cancers.
The definition over the last decade of a multitude of tumor antigens has underscored the importance of creating a proinflammatory immune response to eradicate cancer.
The majority of tumor antigens identified have been self-proteins, and tolerance has emerged as an important mechanism of tumor immune escape.
Thus, methods of generating anticancer immunity must focus on the initiation and maintenance of an inflammatory environment complete with APCs potent enough to stimulate naive T cells, i.e., dendritic cells (DCs).
The potential of DCs in eliciting antitumor immunity has been an area of intense investigation.
DCs are unique in their expression of important costimulatory molecules, the elaboration of proinflammatory cytokines, and the ability to process and present self-antigens (Figure 1).
DCs exist primarily in two distinct phenotypic forms.
Immature DCs are able to circulate through peripheral tissues and sample soluble antigen and possibly necrotic or apoptotic cells.
These DCs express few costimulatory molecules and are unable to prime T cell responses.
Once DCs begin to process and present antigen, they "mature" into a more stellate shape capable of presenting antigen and initiating an adaptive immune response.
The presence of TLRs allows the DC to recognize common molecular patterns found on a variety of pathogenic organisms, so-called pathogen associated molecular patterns.
TLR signaling is thought to represent a major mechanism of innate immunity and is another process that results in antigen-presenting cell (APC) conditioning and release of proinflammatory cytokines.
Maturation of DCs also results in increased expression of MHC, costimulatory molecules, and chemokine receptors that direct DCs to regional lymph nodes where they are more likely to encounter their cognate T cell and are able to prime T cell responses.
The clinical application of DCs in the form of cancer vaccines, however, has been only moderately successful.
The majority of clinical approaches have used ex vivo-derived DCs to elicit tumor-specific immunity.
However, cultured DCs have demonstrated poor homing to lymph nodes once injected in vivo, inconsistent processing and presentation of antigen, antigen, and, depending on their maturation status, the ability to either enhance or inhibit the generation of tumor antigen-specific immunity.
Recently, scientists present a novel approach to overcoming the limitations of ex vivo-derived DCs and in doing so outline a strategy potent enough to influence the local immune microenvironment in an established tumor, which supports the initiation and propagation of an effective tumor-specific immune response.
They demonstrated that the local presence of CC chemokine ligand 20 within immunogenic CT26 tumors attracted a large number of DCs to the tumor site and could mediate tumor regression.
However, poorly immunogenic B16 tumors were not rejected unless local CpG was also injected.
This provides a method for manipulating both the number of local DCs and the local environment, resulting in effective tumor immunity.
Stimulating DCs in vivo may allow natural maturation and retention of their most potent functions and represents a more rational approach to immunotherapy.
The migration of DCs, as well as other immune cells, is mediated by chemokines through a concentration-dependent process attracting cells to sites of chemokine secretion.
Recent evidence suggests that chemokines induce motility, and possibly other proinflammatory and activating processes, through the selected expression of specific membrane receptors.
These receptors may be differentially regulated during different stages of cellular differentiation.
For example, immature DCs circulate through peripheral tissues where they can acquire antigen at sites of inflammation.
As DCs mature, they increase their expression of the CC chemokine receptor 7 (CCR7), which directs their migration to regional lymph nodes where constitutively secreted chemokines attract mature DCs via the CCR7 receptor.
Since naive T cells also express CCR7, the nodal chemokines orchestrate the co-localization of antigen-presenting DCs with T cells, thus increasing the likelihood of DC-T cell interaction and T cell priming.
Several animal models have already demonstrated that chemokine expression within tumors can induce the migration of T cells and APCs to those sites and can mediate modest antitumor responses.
Thus, local expression of chemokines can alter the types of cell present within tumors.
Once appropriate cells are mobilized, they can be further activated or expanded by the use of other potent immune stimulatory molecules, such as cytokines and costimulatory molecules.
In the case of DCs this allows for uptake and presentation of tumor antigens directly from established tumors, avoiding the need for defined antigens.
Furthermore, the DC can be activated at the site of maturation through the co-expression of local costimulatory molecules, proinflammatory cytokines, and Toll-like receptor (TLR) agonists (Figure 2).
The ability to manipulate the type of cells, their maturation status, and functional activity at specific sites may introduce a new therapeutic strategy for manipulation of host immune responses against tumors.
Immunization in the setting of cancer prevention or even in minimal residual disease is now beginning to demonstrate that if the immune-dampening effects of the tumor microenvironment are not operative, cancer vaccines may have clinical impact.
Investigators have reported that immunization of young women with a vaccine targeting human papillomavirus (HPV) 16 protects not only against the development of HPV infection, but most likely against the development of cervical intraepithelial neoplasia.
Furthermore, a recent randomized trial demonstrated that patients with melanoma whose disease had been completely resected and who bore specific HLA immune phenotypes could be immunized with a cell lysate-based vaccine, resulting in a significant survival benefit.
Following successful immunization, the tumor microenvironment is dramatically altered. DC maturation occurs, and the DCs are induced to express strong costimulatory molecules able to effectively prime CD4 and CD8 T cell responses. When CD4 T cells are skewed to a Th1 phenotype, they further promote T cell priming and alter the local cytokine environment by releasing proinflammatory cytokines, such as IFN-g and IL-12. This environment is favorable for tumor cell recognition and results in tumor rejection.
The deliberate manipulation of local immune responses with highly specific molecules and delivery vectors has been able to promote immune-mediated regression of established and poorly immunogenic tumors in mice.
This represents an exciting new strategy for the treatment of human cancer and warrants renewed interest in clinical trials to determine the full potential for these approaches in cancer patients.