Abstract
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Carbon nanotubes as vaccine scaffolds
Abstract
Carbon nanotubes display characteristics that are potentially useful in their development as scaffolds for vaccine compositions. These features include stability in vivo, lack of intrinsic immunogenicity, low toxicity, and the ability to be appended with multiple copies of antigens. In addition, the particulate nature of carbon nanotubes and their unusual properties of rapid entry into antigen-presenting cells, such as dendritic cells, make them especially useful as carriers of antigens. Early attempts demonstrating carbon nanotube-based vaccines can be used in both infectious disease settings and cancer are promising.
1.0 Introduction
Vaccines are drugs designed to elicit a specific, active immune response in a host that will prevent a disease from starting, or lessen the effects of a disease after it has begun. In the field of infectious diseases, nearly all vaccines are administered prophylactically. Such approaches have provided some of the most important advances in human health over the last century. Many attempts also have been made to generate “therapeutic” cancer vaccines for patients who already have a cancer, which could be used to reduce tumor burden, or prevent or slow recurrence of cancers. No such effective specific cancer vaccines are marketed in the USA today.
The immune system is designed to recognize and react with foreign antigens and vaccines are drugs that are engineered to mimic these foreign molecules, so as to direct the specific immune response for therapeutic purposes. Antigens presented by microbes and bacteria are typically more potently immunogenic than self-antigens derived form cancers. In cancer vaccines, the antigens are not foreign, and are usually over-expressed proteins or sugars on the surface or inside the tumor cell. Intracellular proteins from microbes, viruses or cancers can be presented on the cell surface in the context of MHC molecules for T cell recognition1, 2. Presentation by dendritic cells (DCs), which are the most effective antigen presenting cells (APCs)3, 4, drives the initiation of a strong response. Self-antigens are generally weakly immunogenic and the immune system of animals or patients with cancer either does not recognize the antigen, is tolerant to it, or can not mount an adequate cytocidal response5, 6. Soluble molecules are usually weak immunogens; therefore, delivery formulations that include carrier molecules and adjuvants can make more effective immunization strategies. Adjuvants promote a more potent immune response, such as cytokines7, saponins, CpG motifs8, and heat shock proteins9. Synthetic and natural materials, such as dendrimers or keyhole limpet hemocyanin (KLH), have been used as carrier molecules10, 11.
Vaccine carriers that efficiently deliver the antigens into professional antigen presenting cells such as dendritic cells, would be most useful, as presentation of peptide antigens by the MHC molecules of dendritic cells (APC’s) is essential to mounting a potent immune response. Particulate vaccines are a promising approach to improve the immunogenicity of proteins, as the particles improve immune responses. Interestingly, the response is highest when the particles are on the nano-scale, which may relate to the ability of cells to best interact with the vaccine particle of this size12,13,14. Nanoparticulate formulations also can serve as an extracellular or intracellular depot of antigen, which prolongs immune activation.
Carbon nanotubes (CNT) offer a number of features that make them interesting candidate materials for vaccine compositions, as a scaffold to carry the specific antigenic target and to facilitate its presentation to the immune system. CNT are relatively inert and non-immunogenic and non-toxic15-18 by themselves. They are highly stable on the shelf and in vivo. Their unique structures allow highly efficient conjugation of many antigens, simultaneously, and to multiple different antigens at once, to their surfaces. Interestingly, 100% of the structure of single wall CNT is surface atoms. In addition, CNT can be made particulate and insoluble, thereby prolonging effects in vivo as a depot, and promoting engulfment by phagocytic cells involved in the generation of the immune response. Finally, CNT have the interesting property of rapid entry into cells, including dendritic cells, which are essential to the stimulation of effective immune responses19-21.
In this review we discuss various approaches to vaccine development, the current methods to isolate and purify CNT for this purpose, methods to covalently functionalize them with biologically active molecules such as protein antigens, and the early attempt to make vaccines with CNT. The biomedical applications of CNT, including their use as carries for antigens, as immune stimulants, or as inflammatory molecules, have been reviewed several times recently or in this issue15, 18, 22-24. We encourage readers to seek these papers for a broader look at the biomedical applications of CNT.
2.0 Vaccines and adjuvants
Development and application of vaccines against pathogens have achieved a significant success in controlling and preventing life-threatening infectious diseases in the past century25,26. Similarly, the development of cancer vaccines has been of intense research interest in the past few decades and has provided approaches to adjuvant therapy in conjunction with other anti-cancer therapies27. Vaccines normally consist of three components. The first component is represented by one or more specific antigens that can be encoded by DNAs, or are peptides and proteins, or carbohydrates, derived from immune-dominant epitopes identified in pathogens or cancer cells. Upon vaccination, these specific antigens are able to generate specific and long-lasting immune responses against the host cells, whereby destroying either pathogens or cancer cells. The second component of vaccines, which is not always necessary, is a carrier. This is a scaffold, which may be immunogenic on its own and that is used to deliver the antigen to appropriate cells in vivo or retain it at a site. The third important component of vaccines is the adjuvant, which is required for effective vaccine delivery and for inducing robust inflammatory responses.
Effective adjuvants act through multiple mechanisms, including the generation of antigen depots, activation of antigen-presenting cells (APCs) via pattern recognition receptors (PRRs) such as toll-like receptors (TLRs) and enhancing the presentation of vaccine antigens by APCs28,29. In addition to adjuvants with biological functions, the carrier delivery systems included in the vaccine formulation can also help to achieve desired targeting ability, depot and inflammation30. Adjuvants can be generally divided into two categories: immune-stimulatory molecules and antigen delivery vehicles. However, they can exhibit both characteristics simultaneously. Vaccines and adjuvants used in earlier studies are either attenuated pathogens (for example: Coley’s toxins) or adjuvants that are the mixtures of bacterial walls and mineral oil, such as complete or incomplete Freund’s adjuvants. Although it had been a wide-spread practice for immunologists to use adjuvants together with specific vaccines to generate effective immune responses, the mechanisms of their action were poorly understood. The discovery of the TLRs in 1990s, significantly increased the understating of how adjuvants stimulate innate immunity and bridge it to adaptive immunity. Recent advances in nanotechnology have also made it possible for specific, effective and controlled delivery of the vaccines to immune system30.
2.1 Immuno-stimulatory adjuvants
2.1.1 TLR agonists
The immune system recognizes pathogen-associated molecular patterns (PAMPs) expressed by wide variety of infectious microorganisms, by PRRs, which include TLRs, NOD-like receptors (NLRs) and RIG-I-like receptors (RLRs). The use of TLR agonists as adjuvants is based on the knowledge that several TLR ligands are known as PAMPs, and engagement of receptor-ligands activate DCs, macrophages and other innate immune systems that express TLRs on their cell surface or in their intracellular endosomes. Activation of DCs and macrophages results in enhanced phagocytosis of antigens, cytokine production, and up-regulation of co-stimulatory molecules. Subsequently, the host mounts an adaptive immune response, characterized by the expansion of antigen-specific T and B cells, activation of T helper and cytotoxic T cells and production of antibodies, that insure long-lasting immunological memory to protect against infection and cancers. Twelve TLRs and their ligands have been identified in humans31. For example: TLR-3 binds to double strand RNA (dsRNA) in virus, which has been known to induce type I interferons, enhances antigen presentation and the cytotoxicity of NK and T cells. The synthetic dsRNA polyinosinic-polycytidylic acid (Poly I:C) has been tested in pre-clinical studies and in numbers of human clinical trials as an adjuvant to anti-cancer vaccines32,33. TLR4 binds to bacteria lipopolysaccharide (LPS), which is a potent non-specific immunostimulator and is presented in various adjuvants. TLR5 binds to flagellin 34 and TLR9 to unmethylated CPG oligodeoxynucleotide bacterial DNA. TLR-9 agonist CPG-OD represents the most studied and advanced adjuvant candidate35. When used as an adjuvant, CPG motifs stimulate cells that express TLR-9, primarily plasmacytoid DC and B cells, to produce Th1 cytokines, enhances antigen presentation and induction of long-lasting CD8 T cells and Ab production. CPG-ODN has been evaluated as adjuvant in a wide variety of preclinical models and in human clinical trials in both infectious diseases and cancer vaccine therapies35-40.
2.1.2 Cytokines
Cytokines produced by immune cells are important immune-modulators in both innate and adaptive immune responses. Therefore, a number of cytokines have been used as adjuvants to enhance vaccine efficacy41. Granulocyte-macrophage colony-stimulating factor (GM-CSF) is the most widely used adjuvant in human trials, primarily because it can activate macrophages and induce DC differentiation, thus to help initiating an effective Ag-specific immune response. Some reports showed that GM-CSF may induce myeloid suppressor cells, however, the vast majority of studies have shown that GM-CSF enhances cancer vaccine-induced immune responses, when used as an adjuvant42,43. We have evaluated the effects of GM-CSF in MHC class I peptide vaccines derived from BCR.ABL in a mouse model, in combination with TiterMax adjuvant. The mice immunized with peptide/TiterMax plus GM-CSF showed stronger IFN-γ secretion by CD8 T cells than the group without GM-CSF (unpublished). In addition, type I IFNs (IFN-α/β) are pleoitropic innate cytokines that are secreted in response to viral infection. IFN–α/β can up-regulate MHC class I and II expression, induce Th1 T cell helper responses and activate NK cells and CD8 T cell cytotoxicity and therefore, can be the most powerful natural adjuvants of the immune system. IFN-α has successfully been shown to improve the protective immunity of peptide and vector-based vaccines in experimental models. When type I IFNs were used an adjuvant in clinical trials in patients with cancers, both immunological and clinical responses were observed36,44. In addition, interleukin -2 and -12 (IL-2 and IL-12) have also been used as adjuvants in cancer therapy, as both cytokines are potent stimulators for cytotoxicity of CD8 T cells. However, the cytokines have short half-life in vivo, and cause toxicity if administered repeatedly and systemically45-47.
2.1.3 Other adjuvants
QS-21 is a saponin-derived soluble adjuvant. It interacts with cholesterol of cell membrane leading to pore-formation on the membranes thereby enhancing antigen-uptake. QS-21 has been shown to enhance both cellular and humoral immune responses and has been used as an adjuvant in a number of clinical trials, in cancer vaccines including chronic myeloid leukemia (CML), breast, prostate and melanoma, as well as in infectious diseases, such as malaria, influenza and hepatitis B45. However, it can cause pain at injection sites and hemolysis, which limits its use. Interestingly, in our work, when mice were immunized with class I peptide vaccines with QS-21 via footpads, the CD8 T cell response was significantly weaker, compared to the vaccines that included TiterMax (unpublished). This study suggests that better uptake of the antigens is not sufficient; the antigenic depot effect and immune-stimulatory effects provided by TiterMax are also required for inducing a robust vaccine-induced cellular immune response. In addition, aluminum salt-based adjuvants (alum) have been used in many vaccine formulation and are the most widely used adjuvants in humans, including hepatitis B virus (HBV), hepatitis A virus, diphtheria, tetanus, human papilloma virus (HPV), etc48,49. Similarly, Montanide, a mineral oil-based adjuvant, has been widely used in human trials in both cancer vaccines and infectious diseases50. The mechanisms of the action for these adjuvants have been attributed to their ability to provide a long-lasting depot effect, effective Ag uptake and presentation by APCs and activation of APCs50.
2.2 Delivery vehicles as adjuvants
Besides the addition of adjuvants with biological functions, vaccine delivery by use of a carrier system can significantly impact vaccine efficacy, by achieving target specificity, controlling the quantity end timing of vaccines, reducing the unwanted non-specific immune response and enhancing the vaccine-specific immunogenicity. Carriers, such as liposomes, microspheres, proteasomes, virosomes and virus-like particles (VLPs), antigen cochleates, dendrimers and carbon nanotubes have been widely explored for vaccine delivery30,52-54. Single-wall carbon nanotubes (SWNTs) have emerged as a potential vaccine delivery vehicle, given their unique physical and chemical properties. (see discussion in section 5 below.) In choosing a nanomaterial as an adjuvant or carrier one needs to carefully consider the properties of the material as they relate to depot effects (that is, does it retain the antigen in the same site for long periods and does it release the material and by what kinetics?) and inflammatory effects (is the carrier immunogenic by itself or will it enhance or detract from the immunogenicity of the carried antigen?) In principle, an optimal carrier would carry large numbers of antigens and many types of antigens, would retain antigens with slow release over time to allow inflammation at the site, would promote internalization of the antigen into the antigen presenting cell such as a dendritic cell and would not incite a dominant response to itself,
3.0 Purification of Nanotubes
Medical applications of CNT require highly pure and well characterized materials. Whether selecting for length, diameter, chirality, number of walls, metallicity, degree of modification or fidelity, the purification of carbon nanotubes has been a challenge since their discovery, and is today the largest obstacle to their swift translation into useful products. In the following section a number of techniques will be examined in the effective purification of carbon nanotubes that could be useful for vaccines.
3.1 Synthetic Purity
The goal of obviating purification altogether through a uniform synthesis has eluded scientists for the last two decades; however, a number of partially selective syntheses have been developed. Nanotubes are produced by arc discharge using carbon based electrodes impregnated with metal catalysts, or by catalytic methods such as chemical vapor deposition (CVD) and high pressure carbon monoxide (HiPCO) process55. Other techniques such as laser-vaporization and high-temperature heat treatments also exist, but are not as commercially popular56.
These techniques have important general differences in the products they generate. For instance, multi-walled tubes generated by arc discharge tend to have a higher fidelity (fewer defects) than other methods, but their synthesis is not as scalable for mass production as are catalytic synthetic methods. Single wall tubes, however, have similar fidelity regardless of production method57. Such general differences are a starting point for choosing which tubes to purchase.
Within these categories, there are many options for modifying the product. The modification of atmosphere, pressure, temperature, flow rates, catalyst, distance between electrodes, voltage, and electrode doping, among others have influences on the qualities of the nanotubes generated58.
One aspect of selection that has met with success through synthetic modifications is the number of walls in tubes. This has permitted the preferential creation of single, double, and less defined multi-walled tubes. As an example, the selective creation of double-walled tubes was discovered by the inclusion of sulphur in anode catalyst mixtures at low pressures59,60.
Single-walled tubes can be created at greater than 90% exclusivity with control of pressure and the addition of Nickel and Cobalt to Iron catalysts61,62, or by restricting the size of tube seeding nanodots63 . Though far from completely selective, nanotubes have been synthesized with preferential chiralities as well64. Chirality of nanotubes, especially single-walled tubes, determines their electronic properties, and must be controlled if they are to be used in computer chips.
Nanotubes are generated by a variety of methods; each approach has its own profile of properties, proportions and residual impurities. Ultimately, one of the more important aspects of planning a nanotube purification is deciding which type of tubes to purchase initially. If residual metals are more of a concern HiPCO tubes should be avoided as they are furnished with a higher iron content65. If amorphous carbon contamination to multi-walled tubes is an issue then CVD66 tubes should be substituted with those manufactured by arc-discharge.
3.2 The Removal of Amorphous and Graphitic Carbon, and Catalysts from Nanotubes
For medical applications the CNT must be rigorously pure, reproducible and well defined before regulatory agencies will allow their use in humans. The method by which nanotubes are generated, as discussed above, not only determines the properties of the tubes, but also the proportions of metals and other impurities that may need to be removed before the nanotubes can be employed. For instance, metals can interfere with conductivity and radiolabelling, and inclusion of amorphous carbon weakens the mechanical and thermal conductivity properties of nanofibers. Myriad methodologies have been developed to separate carbon nanotubes from metals, sp3 carbon species, graphitic carbon species, and multi-form amorphous carbon. Techniques taking advantage of physical, chemical and electrical differences between tubes and their contaminants have met with success and are often used in combination to produce “pure” (but generally heterogeneous in length and chirality). These methods include acid treatments to remove metals67,68, oxidations to open end caps69,70 and to break the tubes at points of imperfection71,72, filtrations to remove small, often imperfect carbon fragments73, centrifugation74, and covalent and non-covalent modifications that allow separations on the basis of solubility through extraction, gel permeation, filtration, and chromatography75-81. Nanotubes have been heated (annealing)82 or LASERed to high temperatures which also works to remove imperfections and restore conjugation to bent or broken regions through isomerization. A technique currently being development by the Scheinberg lab takes advantage of the bundling properties of functionalized tubes in order to remove impurities through aqueous dialysis (unpublished). In the case of vaccines, once a immunoreactive peptide has been attached to the nanotube, purification of successfully labeled nanotubes could be accomplished through use of affinity columns, though no such work has yet been published on this method.
3.3 Purifications of Chirality
Purifications of a mixture of zigzag, armchair and helical nanotubes are perhaps the most challenging of all separations. It should be noted that perfect armchair and zigzag tubes are not chiral species as they have a mirror plane, but are often spoken of as such in comparing chiralities. Small amounts of tubes of a single chirality can now be separated through ultracentrifugation83 and gel filtration84. Other processes have been developed to create asymmetric tubes out of symmetric ones. Hongjie Dai suspended nanotubes in water in a vertical monolayer and selectively oxidized the ends of the bundles beneath the surface of the water creating a uniformly asymmetric species85. Finally, electric fields can be used to align and order nanotubes both during and after their growth controlling conformation in this case rather than chirality86.
We propose an effective way to separate tubes by their chiralities through chromatographic separation using tubes of a set chirality as a stationary phase. A hefty investment of chiral tubes into a chromatography column with a nanotube stationary phase of set chirality could provide a mechanism for the mass production of chiral tubes. One such product is already in development.
3.4 Assessment of Purity
A number of methods are available to assess the purity of nanotubes and nanotube constructs with the requisite standard being direct visualization through HRTEM, SEM and AFM. Dynamic light scattering87 is used to determine the length distribution of nanotubes; Raman spectroscopy88 elucidates the degree of fullerene-like carbon versus amorphous, graphitic, or sp3 carbon impurities. Near infrared studies89 are best used to determine the gross purity of a sample for which direct visualization studies may be too myopic. The characteristic absorption slope of nanotubes also provides supporting information as to the degree of nanotube modifications. Degrees of modification can also be assessed through chemical tests such as the Kaiser/Sarin assay. When nanotubes are made soluble through modification, HPLC is very useful in the assessment of purity, and can produce discreet peaks even for substances as heterogeneous in structure as carbon nanotubes. Mechanical techniques may also be used to appraise nanotube purity. Measurement of the Young’s modulus, or thermal conductivity may be used as a gross assessment of nanotube purity, but does not clearly identify the problematic factor. Thermogravimetic analysis can provide information on long term stability and potential for oxidation under extreme conditions90-92.
4.0 Functionalization of carbon nanotubes
Pristine carbon nanotubes are chemically inert and extensively aggregate into particulates in aqueous solution under physiological conditions. Chemical modification must be performed to introduce multiple reactive moieties onto either the single-walled and multi-walled CNT surfaces. These reactive functionalities can be employed to further append antigenic peptides, proteins and biologics. Chemical functionalization may also lead to better dispersion of the vaccine and consequently improve antigen presentation in vivo. Needless to say, chemical functionalization provides a means to covalently attach antigens to the CNT platform which yields more stable vaccine composition and unique pharmacokinetic and pharmacodynamic properties.
A rich synthetic organic chemistry of multi-wall and single-wall CNT scaffold modification has been reviewed by Singh et al.93 The introduction of carboxylic acid moieties can be readily accomplished by treating the CNT with strong acid under oxidizing conditions. These acidic groups can further undergo amidation or esterification reactions with thionyl chloride or carbodiimide reagents, respectively to append other groups of biological value. This approach has been used to covalently attach many copies of the polyelectrolyte polyethylene imine94 or proteins obtained from tumor lysates95. Another versatile route is the addition of primary amine groups employing the 1,3-dipolar cycloaddition of reactive azomethine ylides with the carbon-carbon double bonds of the CNT sidewall surface.96 The ylides are generated in situ by thermal condensation of aldehydes and α-amino acids that upon reaction with the CNT surface yield pyrrolidine rings. This latter approach yields water soluble, stable and well dispersed functionalized CNT. The CNT-(NH2)x platform has been used to append peptides via (i) condensation97,98; (ii) chemoselective ligation using bifunctional coupling reagents97-99; and (iii) bio-orthogonal coupling through a hydrazone linkage100. Interestingly, the resultant hydrazone linkage formed between the CNT and the peptide yields a chromophore that can be quantified spectrophotometrically (λmax = 354 nm, ε = 29,000 M−1cm−1) and provides information on the amount of peptide attached per CNT.
CNT-based vaccines that have been built from the ground-up often require several synthetic and purification steps over the course of the production. Thorough characterization of the chemical identities of the starting materials, intermediates, and final products is important in obtaining reproducible and interpretable biological results, given the inherent variability that is observed in immunotherapeutic studies.
5.0 Use of CNT as vaccines in vivo
The ability to link multiple copies of antigens or immune stimulants simultaneously to CNT allows the design of diverse approaches for the use of CNT in vaccine construction. Viral, bacterial and protozoal antigens as well as CpG adjuvants have been appended 94,99,101. One of the early attempts to apply CNT as a scaffold for vaccine development involved the covalent attachment of foot-and-mouth disease viral envelope peptides to CNT97,98. This work showed that it was possible to retain the epitope structure in an immunogenic form when attached to the CNT. Indeed, the CNT-viral protein molecular complexes were capable of generating specific immune responses in animal models. Pantarotto showed that only the peptide-CNT elicited IgG responses which are neutralizing97,98.
Meng et al. used a tumor cell lysate conjugated to single-wall CNT as a therapeutic cancer vaccine in mouse model hepatoma 95. The conjugated vaccine improved cure rates as compared to lysates alone, apparently by improved activation of cytolytic T cells.
Single-wall CNT-PPD antigen was used to study the character of the T cell responses in mice101. Interestingly, while traditional adjuvants such as PPD in Freund’s adjuvant generated a predominately Th-2 response, the single-wall CNT-PPD response was biased toward a Th-1 cytokine response (interferon and IL-12.)
Mocan and others102 compared the effects of multi-wall CNT and embryonic stem cells, injected separately into the same mice to suppress the growth of murine colon carcinoma. This combination was more effective than either agent administered alone, and both CD4 and CD8 activation was enhanced, but whether there is an induction of a specific immune response to the cancer cells was not studied.
The Wilm’s tumor protein (WT1) is over-expressed in many human leukemias and cancers and it is widely used in human trials as a cancer vaccine50,104, 105. Villa et al. aimed to demonstrate that carbon nanotube-peptide constructs could improve the immunogenicity of this weakly immunogenic, clinically relevant cancer-associated peptide100. They used spectrally quantifiable chemical approaches to covalently append large numbers of a 19 amino acid peptide onto solubilized single-wall carbon nanotubes. The nanotube scaffold itself was non-cytotoxic to dendritic cells in vitro and appeared non-immunogenic in mice. The peptide alone with an adjuvant did not induce an immune response in mice. The peptide-single-wall CNT vaccine was internalized into dendritic cells and macrophages within minutes in vitro, which should serve to promote immunization. Mice immunized with the single-wall CNT-peptide vaccine and an adjuvant induced specific IgG responses against the peptide.
In addition they observed that uptake of the vaccine into the dendritic cells or macrophages occurred in 5 min, followed 15 min later by accumulation of the peptide-single wall CNT in a diffuse perinuclear compartment. Microscopic analyses suggested that CNT-peptide constructs were concentrated in intracellular vesicles potentially enhancing peptide delivery into APCs100.
6.0 Conclusions
Numerous approaches to vaccine development are under study including the use of nanoparticles as carriers. Nanomaterials have features that allow them to be effective carriers including multivalency, stability, and a likelihood of internalization into antigen presenting cells. The use of CNT in this regard is just beginning. As carriers alone, or with small molecules attached to them, they clear the blood via the kidney105. However, with larger appended moieties or proteins they are retained within the blood stream. Their unusual property of rapidly internalizing into antigen presenting cells while carrying their cargo is a distinctive advantage to CNT. A better understanding of the specifications that control this process, such as length, charge, hydrophobicity, are required to optimize their use in this regard. Due to their stealthy characteristics, SWNT may not adequately stimulate innate immunity alone as do classic adjuvants or carriers. Therefore, immunologic adjuvants appear necessary for more potent immune responses to CNT-based vaccines, which is not surprising, as adjuvants are necessary for eliciting antibody responses for other vaccines. One advantage though is the ability to conjugate different molecules simultaneously to the nanotube. For example, one could attach both the antigen and the adjuvant or an immune-stimulatory cytokine to the same construct. Importantly, conjugation of the antigen to CNT appears to avoid the use of carrier proteins such as keyhole limpet hemocyanin (KLH). KLH has some features in common with a nanomaterial, such large size and insolubility, but is a biologic material and difficult to access from the sea. Considerable investigation remains to understand the role of CNT in vaccine compositions in comparison to more traditional carriers.
ACKNOWLEDGMENTS
Supported by NIH P01 Ca 23766 and NIH R01 Ca55349, The Experimental Therapeutics Center, and The Tudor and Glades foundations.
Footnotes
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Funding
Funders who supported this work.
NCI NIH HHS (7)
Grant ID: P01 CA023766
Grant ID: P01 CA033049
Grant ID: R01 CA55349
Grant ID: P30 CA008748
Grant ID: T32 CA062948
Grant ID: P01 CA23766
Grant ID: R01 CA055349
NIGMS NIH HHS (1)
Grant ID: T32 GM007739