- Open Access
Intravenous ascorbic acid as an adjuvant to interleukin-2 immunotherapy
Journal of Translational Medicinevolume 12, Article number: 127 (2014)
Interleukin-2 (IL-2) therapy has been demonstrated to induce responses in 10-20% of advanced melanoma and renal cell carcinoma patients, which translates into durable remissions in up to half of the responsers. Unfortunately the use of IL-2 has been associated with severe toxicity and death. It has been previously observed and reported that IL-2 therapy causes a major drop in circulating levels of ascorbic acid (AA). The IL-2 induced toxicity shares many features with sepsis such as capillary leakage, systemic complement activation, and a relatively non-specific rise in inflammatory mediators such as TNF-alpha, C-reactive protein, and in advanced cases organ failure. Animal models and clinical studies have shown rapid depletion of AA in conditions of sepsis and amelioration associated with administration of AA (JTM 9:1-7, 2011). In contrast to other approaches to dealing with IL-2 toxicity, which may also interfere with therapeutic effects, AA possesses the added advantage of having direct antitumor activity through cytotoxic mechanisms and suppression of angiogenesis. Here we present a scientific rationale to support the assessment of intravenous AA as an adjuvant to decrease IL-2 mediated toxicity and possibly increase treatment efficacy.
The basis of cancer therapy is to identify/develop interventions that: a) selectively kill tumor cells while sparing non-malignant cells; b) prevent development of tumor-resistance; and c) act systemically to prevent relapse. Theoretically, immunotherapy of cancer would achieve all these aims. Selective killing of tumor cells has been demonstrated by a wide range of immune cells ranging from conventional CD8 T cells, gamma delta T cells, natural killer (NK) cells, natural killer T (NKT) cells and in some studies neutrophils. Other components of the immune system expressing tumor selectivity include complement factors and natural antibodies of the IgM isotype. Tumor resistance to immunotherapy, differs from resistance to chemotherapy, where expression of multiple drug resistance proteins actively pumps out cancer-toxic substances. One mechanism is downregulation of human leukocyte antigen (HLA) by tumor cells in response to T cell killing. The immune system conceptually overcomes this by the NK subset which preferentially kills cells with downregulated HLA. The other mechanism of tumor resistance from immunological attack is by mutating antigens that are being recognized. Given the promiscuous binding ability of T cell and B cell receptors to bind antigens, the cells could conceptually “mutate with the tumor” in order to recognize and kill cells with variant antigens. Immunological destruction of neoplasia is believed to occur at a systemic level and thus arises the possibility to inhibit metastasis and tumor recurrence, in part through induction of immunological memory.
The history of tumor immunotherapy begins with the work of William Coley who induced a systemic inflammatory/immune activation through administration of killed S. pyogenes and Serratia marcescens bacteria in patients with soft tissue sarcoma . The advent of molecular biology allowed for assessment of molecular signals associated with systemic immune activation. The cytokine tumor necrosis factor (TNF)-alpha was one of the molecular signals associated with anticancer efficacy of innate immune activators such as the Coley vaccine . Studies have demonstrated that TNF-alpha has the ability to induce profound death of cancer cells in vitro and in vivo in animal models, however human studies demonstrated unacceptable levels of toxicity [3–5]. IL-2 was the next cytokine associated with immune activation that was tested. Originally termed T Cell Growth Factor (TCGF) , IL-2 was demonstrated in early studies to endow human lymphocytes with ability to selectively kill tumor but not healthy control cells . Subsequent studies have demonstrated that cytotoxic activity was mediated through T cell and natural killer (NK) cells, whose activation requires stimulation of the IL-2 receptor [8, 9], which can be accomplished in vivo with high doses of IL-2 [10–12]. Animal studies suggested that IL-2 has a short half-life of approximately 2 minutes after intravenous injection [13, 14], and human half life was reported to be approximately an hour . Thus it was apparent that clinical use of IL-2 would be requiring repeated administration at high doses. Despite this pitfall, preclinical studies demonstrated highly potent anti-tumor effect. In 1985 Steven Rosenberg reported regression of established pulmonary metastasis, as well as various subcutaneous tumors by administration of IL-2 . These data were highly promising due to the fact that tumor killing could be achieved systemically, and by activation of specific immune cells that could be identified in vivo as interacting with and inducing death of the tumor.
Early studies of IL-2 demonstrated impressive results in a subset of melanoma and renal cell cancer patients. Development of systemic autoimmunity to melanocytes, such as the occurence of vitiligo during the treatment with systemic IL-2 was found to be predictive of response. These studies were expanded and eventually IL-2 received approval as the first recombinant immunotherapeutic drug by the FDA. There appears to be a dose response with IL-2 in that the doses that seem to be most effective are also associated with significant toxicity. The most significant cause of toxicity is vascular leak syndrome (VSL), manifested as fluid loss into the interstitial space, which is a result of increase vessel permeability. Additional effects include thrombocytopenia, elevated hepatic serum transaminases, hepatocyte necrosis, hypoalbuminemia, tissue and peripheral eosinophilia, and prerenal azotemia .
Vascular leak syndrome
Vascular leak syndrome (VLS) is considered to be the major dose-limiting adverse effect of IL-2 administration. In a meta-analysis of studies performed in metastatic renal cell carcinoma patients, objective responses were observed in 23% of patients, the majority of which lasted more than 10 years . Unfortunately, 65% of patients have to interrupt or stop therapy because of VLS [19, 20]. This syndrome is characterized by an increased extracellular fluid extravasation, hypotension, ascites, pulmonary edema, and hydrothorax [21, 22], and clinically resembles the systemic inflammatory response syndrome (SIRS). Dermatological manifestations include erythrematous eruptions and mild papillary edema associated with burning and pruritus of the skin [23, 24]. Severe forms of VLS are associated with pulmonary or cardiac failure with approximately 1% of treated patients having lethal outcome. Typically the symptoms of VLS are treated by vasopressor therapy and judicious fluid replacement, such as with colloid solutions for their osmotic effects. Patients may also be treated with theophylline and terbutaline, for which clinical experience suggests a possible reduction of the severity and frequency of acute episodes .
Mechanisms of VLS
At a cellular level it is well-known that VLS is associated with endothelial cell activation and increased with vascular permeability. Biopsies of patients receiving IL-2 revealed an increased expression of adhesion molecules such as ICAM and LFA-1. These proteins are known to promote granulocyte extravasation, however, such upregulation was not observed when IL-2 was added directly to endothelial cell cultures in vitro, suggesting the effect was mediated by other host components . Given that one of the main cellular targets of IL-2 is the T cells, which express two types of IL-2 receptor, it appears that the initial T cell activation is a major contributor to downstream inflammatory effect on endothelium subsequent to IL-2 administration. In an early study, Rosenberg’s group established a murine model for quantifying VLS by administering radioactively iodinated albumin into mice receiving IL-2 and assessing radioactivity of tissues, In this model, increased gamma-counts are correlated with endothelial permeability and leakageof albumin into tissues. They found that administration of IL-2 to nude mice or mice that have been immune suppressed by radiation, cyclophosphamide, or steroids, was associated with markedly reduced or no vascular leakage .
T cells and nk cells contribute to endothelial activation
It is possible that the process of LAK generation is involved in stimulation of VLS, as was suggested in a study using a similar system in which transfer of LAK along with administration of IL-2 led to more profound endothelial leakage as compared to either alone. Interestingly, in the same study it was shown that depletion of host lymphocytes reduced vascular leakage only in response to IL-2 alone, but not in response to IL-2 and LAK transfer . Other studies have shown that cells bearing the NK marker asialo-GM1 are associated with some of the IL-2 associated toxicities. Anderson et al showed that antiserum to asialo GM1 suppressed mortality, vascular leak syndrome, hepatic damage and reduced infiltration of pulmonary and hepatic vasculature by asialo GM1+ lymphocytes induced by IL-2 treatment. Depletion of the Asialo-GM1 bearing cells did not alter lymphoid hyperplasia, tissue infiltration by Lyt 2+ lymphocytes, tissue and peripheral eosinophilia, or thrombocytopenia. Interestingly, the antisera did not affect the anti-tumor efficacy of IL-2 therapy in BDF mice bearing the colon 38 adenocarcinoma . Thus it is possible that T cell and NK cell activation by the high dose IL-2 induces production of various cytokines, one example being TNF-alpha , which are known to induce endothelial cell activation locally , and systemically are mediators of SIRS .
Another event associated with IL-2 administration appears to be complement activation. The complement system is an enzymatic cascade of about 30 circulating proteins, primarily generated by the liver that cause inflammation and amplification of a various immune responses. The complement system can be activated through the classical (antibody mediated) pathway, alternative pathways (antibody-independent), or through the mannose-binding lectin pathway, all of which lead to formation of the membrane attack complex which causes cell lysis through generation of pores in the cell membrane . In a clinical study of metastatic renal cancer patients receiving IL-2 via a 24-hour i.v. infusion at a daily dose of 3 × 10(6) U/m2 for 5 consecutive days, the classical complement pathway components C3 and C4 were measured daily during IL-2 infusion, and after its interruption. IL-2 administration was associated with a significant decrease in both C3 and C4 levels, which normalized on average 5 days after the end of IL-2 infusion . Another study associated presence of VLS in patients receiving IL-2 with complement activation as assessed by levels of C3a and the classical complement component C4a. In this study levels of C3a were as elevated as those found in septic and burn patients . Another study examining 23 cancer patients undergoing therapy with interleukin-2 and lymphokine-activated killer cells demonstrated 3-fold elevations of C3a desArg concentrations by the 8th day of therapy with concentrations of C4a desArg also being elevated by the end of therapy. Associated with activation of the complement system was an increase in the neutrophil cell-surface expression of complement receptor Type 1 and complement receptor Type 3 .
This interesting dependence on T cells for complement activation bridges the studies demonstrating that T cells are necessary for both endothelial activation and VLS associated with IL-2 administration. A study by Vachino et al showed that cancer patients had pretreatment similar to control plasma levels of C3a, Ba, Bb, and SC5b-9. Post-IL-2 treatment C3a levels where shown to be increased on average of 15.6-fold (is this differential from controls?). The Ba and Bb proteins, which belong to the alternatively complement activation pathway were augmented 8.0- and 5.0-fold, respectively, subsequent to IL-2 treatment. The plasma levels of the effector complement complex, SC5b-9, was increased 5.0-fold and the plasma C4d and iC3b concentrations increased 4.8- and 2.9-fold, respectively, after treatment. To show the involvement of patient lymphocytes in complement activation, the investigators found that cells expressing the T cell marker CD3 had increased surface expression of anti-C3c and anti-SC5b-9 by 6.2-fold and 5.1-fold, respectively after IL-2 therapy. The authors concluded that the T cells were participating in the IL-2 induced complement activation. This was also demonstrated in that increased concentration of the inflammatory protein C-reactive protein (CRP) was found post-IL-2 therapy , and that the T cells bound CRP. T cell bound CRP was capable of activating the alternative complement pathway . Therapeutically, it was demonstrated that administration of the complement inhibitor C1 esterase inhibitor was capable of reducing IL-2 induced hypotension and complement activation in patients [39, 40].
Complement activates endothelial cells
Various components of the complement cascade have been demonstrated to directly activate endothelial cells, with endothelial cell activation not only causing lymphocyte and neutrophil extravasation, but also thrombosis by the upregulation of tissue factor . C5a is a byproduct of complement activation that has been demonstrated to induce endothelial cell activation and permeability [42–45]. This protein is also a major effector in systemic inflammatory disorders and antibodies to it are being assessed clinically for this condition with some efficacy signals and suppression of endothelial activation published [46, 47]. The complement effector complex SC5b-9 was demonstrated in vitro to induce endothelial cell activation via stimulating expression of the Response Gene to Complement (RGC)-32, which in turn activates CDC2 and the AKT pathway . Jeffrey Platt’s group demonstrated that complement activation is associated with induction of IL-1, which in turn stimulates endothelial cells expression of E-selectin, intracellular adhesion molecule-1, vascular cell adhesion molecule-1, Ikappa-Balpha, interleukin (IL)-1alpha, IL-1beta, IL-8, and tissue factor . Thus in the cascade of IL-2 induced VLS, it appears that T cell activation may be associated with complement activation, and complement activation, in turn, stimulates endothelial cell activation. One of the cardinal features of endothelial cell activation is stimulation of the clotting cascade.
According to the emerging picture that VLS has many common elements with SIRS, one of the common features is development of local thrombocyte and coagulation system activation. Innate immune response possesses the ability to locally marginalize pathogens by stimulation of clotting and consequent sequestration. However, this process becomes pathological when it occurs at a systemic level, such as SIRS or VLS. Upregulation of tissue factor expression was previously noted on endothelial cells from animals treated with IL-2 . Expression of this protein is known to cause activation of the clotting cascade, as well as stimulate inflammatory processes. Hack et al demonstrated activation of the contact system of coagulation proteins by showing that patients on IL-2 therapy had degradation of factor XII and prekallikrein. Reductions in these proteins appeared not due to protein leakage into the interstitial space, since their levels were still significantly lower, i.e., 80 and 50%, respectively, when corrected for albumin decreases (endothelium may still be more permeable to these clotting factors than to albumin, that’s why i would prefer “appeared”) . Thus it appears that non-specific activation of the coagulation system, and a resulting potential for thrombosis, occur as a result of IL-2 treatment. Given the inherently pro-thrombotic state of many cancer patients, it is theoretically possible that IL-2 therapy may have thrombotic complications, which indeed have previously been reported .
Granulocyte activation and tissue infiltration are hallmarks of systemic immune/inflammatory activation. In a study of 4 patients on IL-2, granulocytes became activated following IL-2 treatment with mean peak elastase/alpha 1-antitrypsin (E alpha 1 A) and lactoferrin values of 212 (SEM = 37) and 534 (SEM = 92) ng ml-1 respectively occurring 6 h after the IL-2. Activation of the complement cascade was evidenced by a dose dependent elevation of peak C3a values on day 5 of IL-2. The authors found that there was a significant correlation between C3a levels and the degree of hypotension during the first 24 h after IL-2 (r = 0.91) and parameters of capillary leakage such as weight gain and fall in serum albumin (r = 0.71). The authors concluded that activation of PMN initiates endothelial cell damage which subsequently leads to activation of the complement cascade . Another study showed that neutrophils of patients on IL-2 therapy expressed both phenotypic (up-regulation of CD11b/CD18 adhesion receptor expression) and functional (hydrogen peroxide and hypochlorous acid production) evidence of potent neutrophil activation .
Gut bacterial translocation
Gut bacterial translocation is associated with chronic inflammatory states such as heart failure  and mucositis , and acute states such as sepsis  or GVHD , is translocation of bacterial flora into systemic circulation. Interestingly, IL-2 toxicity is associated with an interference with the gut flora and inflammation. In a recent study, 51 male rats were randomized to receive rIL-2 by intraperitoneal injection at doses (IU) of 10(5) (n = 15), 10(4) (n = 8), 10(3) (n = 8) or 10(2) (n = 8) twice daily, or a saline bolus (n = 12). After 5 days, ileal histomorphology was assessed and the mesenteric lymph node complex was cultured. Results showed that colonisation of mesenteric lymph nodes with Escherichia coli occurred in all rats treated with 10(5) IU of rIL-2, and in 62%, 37% and 12% of rats treated with decreasing doses of rIL-2. No translocation was observed in control animals. An increase in submucosal lymphatics and occasional mucosal disruption was seen only in the group receiving 10(5) IU. These data show that rIL-2 promotes bacterial translocation and suggests a mechanism that may fuel high-dose rIL-2 toxicity in humans . Given the potent effects seen clinically with homeostatically-induced lymphocyte activation , and the recent findings that T cell homeostatic proliferation appears to be associated with gut flora translocation , it may be possible that tumor suppressive activity of IL-2 may be highly dependent on the gut flora, thus possibly explaining inter-patient variation.
Numerous studies have demonstrated that oxidative stress modifies endothelial cells in a manner that preferentially activates the complement cascade . The involvement of the mannose-binding lectin and the lectin complement pathway (LCP) in promoting complement activation by endothelial cells post oxidative stress was shown in studies using hypoxic (24 hours; 1% O(2))/reoxygenated (3 hours; 21% O(2)) human endothelial cells. Using iC3b deposition as a marker of complement activation, it was shown that N-acetyl-D-glucosamine or D-mannose, but not L-mannose, blocked activation, suggesting that oxidative stress upregulates the mannose dependent pathway. This was also demonstrated using mannose binding lectin deficient serum, as well as antibodies to mannose binding lectin. Furthermore C3 deposition was found in ischemic areas in rats that experienced cardiac ischemia reperfusion injury, a known inducer of oxidative stress .
Vitamin C Depletion after IL-2 therapy
The initial stimulus for writing this review was inspired by the observations made by two of the authors (DTA, CAD) of a scurvy-like condition in a renal cell carcinoma patient treated with IL-2. The patient presented with acute signs and symptoms of scurvy (perifollicular petechiae, erythema, gingivitis and bleeding). Serum ascorbate levels were significantly reduced to almost undetectable levels during the treatment with IL-2 . Although the role of ascorbic acid (AA) hyper-supplementation in stimulation of immunity in healthy subjects is controversial, it is well established that AA deficiency is associated with impaired cell mediated immunity. This has been demonstrated in numerous studies showing that deficiency of this vitamin suppresses T cytotoxic responses, delayed type hypersensitivity, and bacterial clearance . Additionally, it is well-known that NK activity, which mediates IL-2 anti-tumor activity, is suppressed during conditions of AA deficiency . Thus it may be that while IL-2 therapy on the one hand is stimulating T and NK function, the systemic inflammatory syndrome-like effects of this treatment may actually be suppressed by induction of a negative feedback loop. This negative feedback loop with IL-2 therapy was successfully overcome by work using low dose histamine to inhibit IL-2 mediated immune suppression, which led to the “drug” Ceplene (histamine dichloride) receiving approval as an IL-2 adjuvant for treatment of AML .
The concept of AA deficiency subsequent to IL-2 therapy was reported previously by another group. Marcus et al evaluated 11 advanced cancer patients suffering from melanoma, renal cell carcinoma and colon cancer being on a 3 phase immunotherapeutic program consisting of: a) 5 days of i.v. high-dose (10(5) units/kg every 8 h) interleukin 2, (b) 6 1/2 days of rest plus leukapheresis; and (c) 4 days of high-dose interleukin 2 plus three infusions of autologous lymphokine-activated killer cells. Mean plasma ascorbic acid levels were normal (0.64 +/- 0.25 mg/dl) before therapy. Mean levels dropped by 80% after the first phase of treatment with high-dose interleukin 2 alone (0.13 +/- 0.08 mg/dl). Subsequently plasma ascorbic acid levels remained severely depleted (0.08 to 0.13 mg/dl) throughout the remainder of the treatment, becoming undetectable (less than 0.05 mg/dl) in eight of 11 patients during this time. Importantly, blood pantothenate and plasma vitamin E remained within normal limits in all 11 patients throughout the phases of therapy, suggesting the hypovitaminosis was specific for AA. Strikingly, responders (n = 3) differed from nonresponders (n = 8) in that plasma ascorbate levels in the former recovered to at least 0.1 mg/dl (frank clinical scurvy) during Phases 2 and 3, whereas levels in the latter fell below this level . Similar results were reported in another study by the same group examining an additional 15 patients . The hypothesis that prognosis was related to AA levels is intriguing because of the possibility of higher immune response in these patients, however this has not been tested.
AA protects the endothelium from inflammation
The main cause of VSL is increased permeability of the endothelium. Regardless of if the initiating cause is T cell activation, complement, and/or oxidative stress, the effector mechanism of VLS is alteration of endothelial cell function. In SIRS the endothelium is also the main effector causing lethality. Methods by which these cells are altered by both SIRS and IL-2 include: a) endothelial cell apoptosis, b )upregulation of adhesion molecules, and c) increased procoagulant state .
It was shown that in vitro administration of AA led to reduction of TNF-alpha induced endothelial cell apoptosis . The effect was mediated in part through suppression of the mitochondria-initiated apoptotic pathway as evidenced by reduced caspase-9 activation and cytochrome c release. Another study examined 34 patients with NYHA class III and IV heart failure who received AA or placebo treatment. AA treatment (2.5 g administered intravenously and 3 days of 4 g per day oral AA) resulted in reduction in circulating apoptotic endothelial cells in the treated but this was not observed in the placebo control group . Various mechanisms for inhibition of endothelial cell apoptosis by AA have been proposed including upregulation of the anti-apoptotic protein bcl-2  and the Rb protein, suppression of p53 , and increasing numbers of newly formed endothelial progenitor cells .
AA has been demonstrated to reduce endothelial cell expression of the adhesion molecule ICAM-1 in response to TNF-alpha in vitro in human umbilical vein endothelial (HUVEC) cells (HUVEC) . By reducing adhesion molecule expression, AA suppresses systemic neutrophil extravasation during sepsis, especially in the lung . Other endothelial effects of AA include suppression of tissue factor upregulation in response to inflammatory stimuli , an effect expected to prevent the hypercoaguable state. Furthermore, ascorbate supplementation has been directly implicated in suppressing endothelial permeability in the face of inflammatory stimuli [78–80], which would hypothetically reduce vascular leakage. Given the importance of NF-kappa B signaling in coordinating endothelial inflammatory changes [81–83], it is important to note that AA at pharmacologically attainable concentrations has been demonstrated to specifically inhibit this transcription factor in endothelial cells . Several pathways of inhibition have been identified including reduction of i-kappa B phosphorylation and subsequent degradation , and suppression of activation of the upstream p38 MAPK pathway . In vivo data in support of eventual use in humans has been reported showing that administration of 1 g per day AA in hypercholesterolemic pigs results in suppression of endothelial NF-kappa B activity, as well as increased eNOS, NO, and endothelial function . In another porcine study, renal stenosis was combined with a high cholesterol diet to mimic renovascular disease. AA administered i.v. resulted in suppression of NF-kappa B activation in the endothelium, an effect associated with improved vascular function .
AA Suppresses Systemic Inflammation
The possibility that IL-2 therapy induces a state of systemic inflammation similar to SIRS has been discussed previously. One of the fundamental questions is whether AA actually has beneficial effects on the process of systemic inflammation. A mouse study demonstrated that after challenge with the bacteria Klebsiella pneumonia to induce a sepsis-like state, a 3-fold higher mortality is observed in ascorbate-deficient animals compared to controls . Another study hyper-supplemented animals with AA by administration of 10 mg/kg AA intravenously before induction of sepsis. IV AA treated animals had a 50% survival while only 19% of control animals survived . Other studies demonstrated that hyper-supplementation with AA resulted in better outcomes in sepsis-associated hypoglycemia , microcirculatory abnormalities , and blunted endothelial responsiveness [93–95] in animal models.
Randomized clinical trials have been performed in septic patients using AA and vitamin E, which demonstrated superior outcomes, as well as reduction in parameters of oxidative stress [96, 97]. To date we know of one study in the recent history that assessed AA alone in patients with systemic inflammation. The investigators examined burn patients with > 30% of their total body surface area affected. Patients were administered intravenous AA i.v. (66 mg/kg/hr for 24 hours, n = 19) or received only standard care (controls, n = 18). AA treatment resulted in statistically significant reductions in 24 hr total fluid infusion volume, and fluid retention (indicative of vascular leakage). Perhaps most striking was the decrease in the need for mechanical ventilation: the treated group required an average of average of 12.1 ± 8.8 days, while the control group required 21.3 ± 15.6 days . Given that numerous inflammatory markers associated with VLS are also found in SIRS and severe burn patients, the possibility is presented that AA may exert some beneficial effects on IL-2 therapy, both from the reduction of toxicity perspective, as well as from the stimulation of efficacy.
We have previously reviewed the rationale for use of IV AA in cancer patients, which includes direct tumor cytotoxicity, antiangiogenic activities, and possibility of increasing quality of life. IL-2 therapy, although one of the oldest successes of cancer immunotherapy, to date, is still not widely implemented due to substantial associated toxicity. To date one drug (Ceplene, histamine dichloride) has succeeded the regulatory and clinical threshold as an agent to reduce IL-2 toxicity and enhance efficacy, thus establishing a regulatory pathway for development of such an agent. In contrast to Ceplene, IV AA is commonly used in the treatment of cancer patients by alternative medicine practitioners, internationally and in the US. Several ongoing FDA clinical trials are currently assessing IV AA as a monotherapy or adjuvant therapy in cancer [99–105]. The rationale that AA preserves endothelial function, inhibits inflammation, and is effective in some states of systemic inflammation, suggests that investigations showed be performed at least in animal models. Our observation of a scurvy-like state induced by IL-2 therapy, the correlation between IL-2 levels and response to immunotherapy, and the fact that IV AA is already clinically used in cancer patients, suggests that translation of the IV AA + IL-2 therapy can be performed in a relatively rapid manner.
Hoption Cann SA, Van Netten JP, Van Netten C: Dr William Coley and tumour regression: a place in history or in the future. Postgrad Med J. 2003, 79: 672-680.
Wiemann B, Starnes CO: Coley’s toxins, tumor necrosis factor and cancer research: a historical perspective. Pharmacol Ther. 1994, 64: 529-564. 10.1016/0163-7258(94)90023-X.
Balkwill F: Tumour necrosis factor and cancer. Nat Rev Cancer. 2009, 9: 361-371. 10.1038/nrc2628.
Mueller H: Tumor necrosis factor as an antineoplastic agent: pitfalls and promises. Cell Mol Life Sci. 1998, 54: 1291-1298. 10.1007/s000180050255.
Taguchi T, Sohmura Y: Clinical studies with TNF. Biotherapy. 1991, 3: 177-186. 10.1007/BF02172090.
Ruscetti FW, Gallo RC: Human T-lymphocyte growth factor: regulation of growth and function of T lymphocytes. Blood. 1981, 57: 379-394.
Lotze MT, Grimm EA, Mazumder A, Strausser JL, Rosenberg SA: Lysis of fresh and cultured autologous tumor by human lymphocytes cultured in T-cell growth factor. Cancer Res. 1981, 41: 4420-4425.
Robb RJ, Munck A, Smith KA: T cell growth factor receptors. Quantitation, specificity, and biological relevance. J Exp Med. 1981, 154: 1455-1474. 10.1084/jem.154.5.1455.
Miyawaki T, Yachie A, Uwadana N, Ohzeki S, Nagaoki T, Taniguchi N: Functional significance of Tac antigen expressed on activated human T lymphocytes: Tac antigen interacts with T cell growth factor in cellular proliferation. J Immunol. 1982, 129: 2474-2478.
Eberlein TJ, Rodrick ML, Massaro AF, Jung SE, Mannick JA, Schoof DD: Immunomodulatory effects of systemic low-dose recombinant interleukin-2 and lymphokine-activated killer cells in humans. Cancer Immunol Immunother. 1989, 30: 145-150. 10.1007/BF01669422.
Ting CC, Hargrove ME, Stephany D: Generation of activated killer cells in tumor-bearing hosts. Int J Cancer. 1987, 39: 232-239. 10.1002/ijc.2910390218.
Fletcher M, Goldstein AL: Recent advances in the understanding of the biochemistry and clinical pharmacology of interleukin-2. Lymphokine Res. 1987, 6: 45-57.
Chang AE, Hyatt CL, Rosenberg SA: Systemic administration of recombinant human interleukin-2 in mice. J Biol Response Mod. 1984, 3: 561-572.
Donohue JH, Rosenberg SA: The fate of interleukin-2 after in vivo administration. J Immunol. 1983, 130: 2203-2208.
Cheever MA, Thompson JA, Kern DE, Greenberg PD: Interleukin 2 (IL 2) administered in vivo: influence of IL 2 route and timing on T cell growth. J Immunol. 1985, 134: 3895-3900.
Rosenberg SA, Mule JJ, Spiess PJ, Reichert CM, Schwarz SL: Regression of established pulmonary metastases and subcutaneous tumor mediated by the systemic administration of high-dose recombinant interleukin 2. J Exp Med. 1985, 161: 1169-1188. 10.1084/jem.161.5.1169.
Mier JW, Aronson FR, Numerof RP, Vachino G, Atkins MB: Toxicity of immunotherapy with interleukin-2 and lymphokine-activated killer cells. Pathol Immunopathol Res. 1988, 7: 459-476. 10.1159/000157075.
Elias L, Hunt WC: A literature analysis of prognostic factors for response and quality of response of patients with renal cell carcinoma to interleukin-2-based therapy. Oncology. 2001, 61: 91-101. 10.1159/000055359.
Bascon JU: Vascular leak syndrome: a troublesome side effect of immunotherapy. Immunopharmacology. 1998, 39: 255-257.
Baluna R, Vitetta ES: Vascular leak syndrome: a side effect of immunotherapy. Immunopharmacology. 1997, 37: 117-132. 10.1016/S0162-3109(97)00041-6.
West WH, Tauer KW, Yannelli JR, Marshall GD, Orr DW, Thurman GB, Oldham RK: Constant-infusion recombinant interleukin-2 in adoptive immunotherapy of advanced cancer. N Engl J Med. 1987, 316: 898-905. 10.1056/NEJM198704093161502.
Rosenberg SA, Lotze MT, Mule JJ: NIH conference. New approaches to the immunotherapy of cancer using interleukin-2. Ann Intern Med. 1988, 108: 853-864. 10.7326/0003-4819-108-6-853.
Gaspari AA, Lotze MT, Rosenberg SA, Stern JB, Katz SI: Dermatologic changes associated with interleukin 2 administration. JAMA. 1987, 258: 1624-1629. 10.1001/jama.1987.03400120074028.
Vial T, Descotes J: Clinical toxicity of interleukin-2. Drug Saf. 1992, 7: 417-433. 10.2165/00002018-199207060-00004.
Druey KM, Greipp PR: Narrative review: the systemic capillary leak syndrome. Ann Intern Med. 2010, 153: 90-98. 10.7326/0003-4819-153-2-201007200-00005.
Cotran RS, Pober JS, Gimbrone MA, Springer TA, Wiebke EA, Gaspari AA, Rosenberg SA, Lotze MT: Endothelial activation during interleukin 2 immunotherapy. A possible mechanism for the vascular leak syndrome. J Immunol. 1988, 140: 1883-1888.
Rosenstein M, Ettinghausen SE, Rosenberg SA: Extravasation of intravascular fluid mediated by the systemic administration of recombinant interleukin 2. J Immunol. 1986, 137: 1735-1742.
Ettinghausen SE, Puri RK, Rosenberg SA: Increased vascular permeability in organs mediated by the systemic administration of lymphokine-activated killer cells and recombinant interleukin-2 in mice. J Natl Cancer Inst. 1988, 80: 177-188. 10.1093/jnci/80.3.177.
Anderson TD, Hayes TJ, Gately MK, Bontempo JM, Stern LL, Truitt GA: Toxicity of human recombinant interleukin-2 in the mouse is mediated by interleukin-activated lymphocytes. Separation of efficacy and toxicity by selective lymphocyte subset depletion. Lab Invest. 1988, 59: 598-612.
Dubinett SM, Huang M, Lichtenstein A, McBride WH, Wang J, Markovitz G, Kelley D, Grody WW, Mintz LE, Dhanani S: Tumor necrosis factor-alpha plays a central role in interleukin-2-induced pulmonary vascular leak and lymphocyte accumulation. Cell Immunol. 1994, 157: 170-180. 10.1006/cimm.1994.1214.
Dinarello CA, Gelfand JA, Wolff SM: Anticytokine strategies in the treatment of the systemic inflammatory response syndrome. JAMA. 1993, 269: 1829-1835. 10.1001/jama.1993.03500140081040.
Salgado A, Boveda JL, Monasterio J, Segura RM, Mourelle M, Gomez-Jimenez J, Peracaula R: Inflammatory mediators and their influence on haemostasis. Haemostasis. 1994, 24: 132-138.
Basiglio CL, Arriaga SM, Pelusa F, Almara AM, Kapitulnik J, Mottino AD: Complement activation and disease: protective effects of hyperbilirubinaemia. Clin Sci (Lond). 2009, 118: 99-113. 10.1042/CS20080540.
Lissoni P, Barni S, Cattaneo G, Archili C, Crispino S, Tancini G, D’Angelo L, Magni S, Fiorelli G: Activation of the complement system during immunotherapy of cancer with interleukin-2: a possible explanation of the capillary leak syndrome. Int J Biol Markers. 1990, 5: 195-197.
Thijs LG, Hack CE, Strack RJ, Van Schijndel JH, Nuijens GJ, Wolbink AJ, Eerenberg-Belmer , Van der Vall H, Wagstaff J: Activation of the complement system during immunotherapy with recombinant IL-2. Relation to the development of side effects. J Immunol. 1990, 144: 2419-2424.
Moore FD, Schoof DD, Rodrick M, Eberlein TJ: The systemic complement activation caused by interleukin-2/lymphokine-activated killer-cell therapy of cancer causes minimal systemic neutrophil activation. Int J Cancer. 1991, 49: 504-508. 10.1002/ijc.2910490405.
Deehan DJ, Heys SD, Simpson W, Herriot R, Broom J, Eremin O: Correlation of serum cytokine and acute phase reactant levels with alterations in weight and serum albumin in patients receiving immunotherapy with recombinant IL-2. Clin Exp Immunol. 1994, 95: 366-372.
Vachino G, Gelfand JA, Atkins MB, Tamerius JD, Demchak P, Mier JW: Complement activation in cancer patients undergoing immunotherapy with interleukin-2 (IL-2): binding of complement and C-reactive protein by IL-2-activated lymphocytes. Blood. 1991, 78: 2505-2513.
Ogilvie AC, Baars JW, Eerenberg AJ, Hack CE, Pinedo HM, Thijs LG, Wagstaff J: A pilot study to evaluate the effects of C1 esterase inhibitor on the toxicity of high-dose interleukin 2. Br J Cancer. 1994, 69: 596-598. 10.1038/bjc.1994.109.
Hack CE, Ogilvie AC, Eisele B, Jansen PM, Wagstaff J, Thijs LG: Initial studies on the administration of C1-esterase inhibitor to patients with septic shock or with a vascular leak syndrome induced by interleukin-2 therapy. Prog Clin Biol Res. 1994, 388: 335-357.
Ward PA: The harmful role of c5a on innate immunity in sepsis. J Innate Immun. 2010, 2: 439-445. 10.1159/000317194.
Gasque P, Singhrao SK, Neal JW, Gotze O, Morgan BP: Expression of the receptor for complement C5a (CD88) is up-regulated on reactive astrocytes, microglia, and endothelial cells in the inflamed human central nervous system. Am J Pathol. 1997, 150: 31-41.
De Jong HK, van der Poll T, Wiersinga WJ: The systemic pro-inflammatory response in sepsis. J Innate Immun. 2010, 2: 422-430. 10.1159/000316286.
Skeie JM, Fingert JH, Russell SR, Stone EM, Mullins RF: Complement component C5a activates ICAM-1 expression on human choroidal endothelial cells. Invest Ophthalmol Vis Sci. 2010, 51: 5336-5342. 10.1167/iovs.10-5322.
Kurihara R, Yamaoka K, Sawamukai N, Shimajiri S, Oshita K, Yukawa S, Tokunaga M, Iwata S, Saito K, Chiba K, Tanaka Y: C5a promotes migration, proliferation, and vessel formation in endothelial cells. Inflamm Res. 2010, 59: 659-666. 10.1007/s00011-010-0178-4.
Conway Morris A, Kefala K, Wilkinson TS, Dhaliwal K, Farrell L, Walsh T, Mackenzie SJ, Reid H, Davidson DJ, Haslett C, Rossi AG, Sallenave JM, Simpson AJ: C5a mediates peripheral blood neutrophil dysfunction in critically ill patients. Am J Respir Crit Care Med. 2009, 180: 19-28. 10.1164/rccm.200812-1928OC.
Helley D, De Latour RP, Porcher R, Rodrigues CA, Galy-Fauroux I, Matheron J, Duval A, Schved JF, Fischer AM, Socie G: Evaluation of hemostasis and endothelial function in patients with paroxysmal nocturnal hemoglobinuria receiving eculizumab. Haematologica. 2010, 95: 574-581. 10.3324/haematol.2009.016121.
Fosbrink M, Cudrici C, Tegla CA, Soloviova K, Ito T, Vlaicu S, Rus V, Niculescu F, Rus H: Response gene to complement 32 is required for C5b-9 induced cell cycle activation in endothelial cells. Exp Mol Pathol. 2009, 86: 87-94. 10.1016/j.yexmp.2008.12.005.
Saadi S, Holzknecht RA, Patte CP, Platt JL: Endothelial cell activation by pore-forming structures: pivotal role for interleukin-1alpha. Circulation. 2000, 101: 1867-1873. 10.1161/01.CIR.101.15.1867.
Trichonas G, Manola A, Morizane Y, Thanos A, Koufomichali X, Papakostas TD, Montezuma S, Young L, Miller JW, Gragoudas E, Vavvas D: A novel nonradioactive method to evaluate vascular barrier breakdown and leakage. Invest Ophthalmol Vis Sci. 2010, 51: 1677-1682. 10.1167/iovs.09-4193.
Hack CE, Wagstaff J, StrackvanSchijndel RJ, Eerenberg AJ, Pinedo HM, Thijs LG, Nuijens JH: Studies on the contact system of coagulation during therapy with high doses of recombinant IL-2: implications for septic shock. Thromb Haemost. 1991, 65: 497-503.
Hotton KM, Khorsand M, Hank JA, Albertini M, Kim KM, Wilding G, Salamat MS, Larson M, Sondel P, Schiller JH: A phase Ib/II trial of granulocyte-macrophage-colony stimulating factor and interleukin-2 for renal cell carcinoma patients with pulmonary metastases: a case of fatal central nervous system thrombosis. Cancer. 2000, 88: 1892-1901. 10.1002/(SICI)1097-0142(20000415)88:8<1892::AID-CNCR19>3.0.CO;2-2.
Baars JW, Hack CE, Wagstaff J, Eerenberg-Belmer AJ, Wolbink GJ, Thijs LG, StrackvanSchijndel RJ, van der Vall HL, Pinedo HM: The activation of polymorphonuclear neutrophils and the complement system during immunotherapy with recombinant interleukin-2. Br J Cancer. 1992, 65: 96-101. 10.1038/bjc.1992.18.
Carey PD, Wakefield CH, Guillou PJ: Neutrophil activation, vascular leak toxicity, and cytolysis during interleukin-2 infusion in human cancer. Surgery. 1997, 122: 918-926. 10.1016/S0039-6060(97)90333-0.
Sandek A, Bauditz J, Swidsinski A, Buhner S, Weber-Eibel J, Von Haehling S, Schroedl W, Karhausen T, Doehner W, Rauchhaus M, Poole-Wilson P, Volk HD, Lochs H, Anker SD: Altered intestinal function in patients with chronic heart failure. J Am Coll Cardiol. 2007, 50: 1561-1569. 10.1016/j.jacc.2007.07.016.
Van Vliet MJ, Harmsen HJ, De Bont ES, Tissing WJ: The role of intestinal microbiota in the development and severity of chemotherapy-induced mucositis. PLoS Pathog. 2010, 6: e1000879-10.1371/journal.ppat.1000879.
Tsujimoto H, Ono S, Mochizuki H: Role of translocation of pathogen-associated molecular patterns in sepsis. Dig Surg. 2009, 26: 100-109. 10.1159/000206143.
Faulkner L, Rapson N, Moore R, Cohen J: The influence of the gut flora on graft versus host disease (GvHD) following allogeneic bone marrow transplantation--experimental observations and possible mechanisms. Prog Clin Biol Res. 1988, 272: 195-206.
Reynolds JV, Murchan P, Leonard N, Gough DB, Clarke P, Keane FB, Tanner WA: High-dose interleukin 2 promotes bacterial translocation from the gut. Br J Cancer. 1995, 72: 634-636. 10.1038/bjc.1995.385.
Appay V, Voelter V, Rufer N, Reynard S, Jandus C, Gasparini D, Lienard D, Speiser DE, Schneider P, Cerottini JC, Romero P, Leyvraz S: Combination of transient lymphodepletion with busulfan and fludarabine and peptide vaccination in a phase I clinical trial for patients with advanced melanoma. J Immunother. 2007, 30: 240-250. 10.1097/01.cji.0000211332.68643.98.
Paulos CM, Wrzesinski C, Kaiser A, Hinrichs CS, Chieppa M, Cassard L, Palmer DC, Boni A, Muranski P, Yu Z, Gattinoni L, Antony PA, Rosenberg SA, Restifo NP: Microbial translocation augments the function of adoptively transferred self/tumor-specific CD8+ T cells via TLR4 signaling. J Clin Invest. 2007, 117: 2197-2204. 10.1172/JCI32205.
Collard CD, Lekowski R, Jordan JE, Agah A, Stahl GL: Complement activation following oxidative stress. Mol Immunol. 1999, 36: 941-948. 10.1016/S0161-5890(99)00116-9.
Collard CD, Vakeva A, Morrissey MA, Agah A, Rollins SA, Reenstra WR, Buras JA, Meri S, Stahl GL: Complement activation after oxidative stress: role of the lectin complement pathway. Am J Pathol. 2000, 156: 1549-1556. 10.1016/S0002-9440(10)65026-2.
Alexandrescu DT, Dasanu CA, Kauffman CL: Acute scurvy during treatment with interleukin-2. Clin Exp Dermatol. 2009, 34: 811-814. 10.1111/j.1365-2230.2008.03052.x.
Anthony HM, Schorah CJ: Severe hypovitaminosis C in lung-cancer patients: the utilization of vitamin C in surgical repair and lymphocyte-related host resistance. Br J Cancer. 1982, 46: 354-367. 10.1038/bjc.1982.211.
McMurray DN: Cell-mediated immunity in nutritional deficiency. Prog Food Nutr Sci. 1984, 8: 193-228.
Ichim ET, Koos D: US Patent No: 20140065096 A1. 2014, Patent and Trademark Office: Washington, DC: U.S, http://www.google.com/patents/US20140065096, accessed 12/15/2010
Marcus SL, Dutcher JP, Paietta E, Ciobanu N, Strauman J, Wiernik PH, Hutner SH, Frank O, Baker H: Severe hypovitaminosis C occurring as the result of adoptive immunotherapy with high-dose interleukin 2 and lymphokine-activated killer cells. Cancer Res. 1987, 47: 4208-4212.
Marcus SL, Petrylak DP, Dutcher JP, Paietta E, Ciobanu N, Strauman J, Wiernik PH, Hutner SH, Frank O, Baker H: Hypovitaminosis C in patients treated with high-dose interleukin 2 and lymphokine-activated killer cells. Am J Clin Nutr. 1991, 54: 1292S-1297S.
Keel M, Trentz O: Pathophysiology of polytrauma. Injury. 2005, 36: 691-709. 10.1016/j.injury.2004.12.037.
Rossig L, Hoffmann J, Hugel B, Mallat Z, Haase A, Freyssinet JM, Tedgui A, Aicher A, Zeiher AM, Dimmeler S: Vitamin C inhibits endothelial cell apoptosis in congestive heart failure. Circulation. 2001, 104: 2182-2187. 10.1161/hc4301.098284.
Haendeler J, Zeiher AM, Dimmeler S: Vitamin C and E prevent lipopolysaccharide-induced apoptosis in human endothelial cells by modulation of Bcl-2 and Bax. Eur J Pharmacol. 1996, 317: 407-411. 10.1016/S0014-2999(96)00759-5.
Saeed RW, Peng T, Metz CN: Ascorbic acid blocks the growth inhibitory effect of tumor necrosis factor-alpha on endothelial cells. Exp Biol Med (Maywood). 2003, 228: 855-865.
Fiorito C, Rienzo M, Crimi E, Rossiello R, Balestrieri ML, Casamassimi A, Muto F, Grimaldi V, Giovane A, Farzati B, Mancini FP, Napoli C: Antioxidants increase number of progenitor endothelial cells through multiple gene expression pathways. Free Radic Res. 2008, 42: 754-762. 10.1080/10715760802357057.
Mo SJ, Son EW, Rhee DK, Pyo S: Modulation of TNF-alpha-induced ICAM-1 expression, NO and H2O2 production by alginate, allicin and ascorbic acid in human endothelial cells. Arch Pharm Res. 2003, 26: 244-251. 10.1007/BF02976837.
Martin WJ: 2nd Neutrophils kill pulmonary endothelial cells by a hydrogen-peroxide-dependent pathway, An in vitro model of neutrophil-mediated lung injury. Am Rev Respir Dis. 1984, 130: 209-213.
Chen YH, Lin SJ, Chen YL, Liu PL, Chen JW: Anti-inflammatory effects of different drugs/agents with antioxidant property on endothelial expression of adhesion molecules. Cardiovasc Hematol Disord Drug Targets. 2006, 6: 279-304. 10.2174/187152906779010737.
May JM, Qu ZC: Ascorbic acid prevents increased endothelial permeability caused by oxidized low density lipoprotein. Free Radic Res. 2010, 44: 1359-1368. 10.3109/10715762.2010.508496.
Wilson JX: Mechanism of action of vitamin C in sepsis: ascorbate modulates redox signaling in endothelium. Biofactors. 2009, 35: 5-13. 10.1002/biof.7.
Utoguchi N, Ikeda K, Saeki K, Oka N, Mizuguchi H, Kubo K, Nakagawa S, Mayumi T: Ascorbic acid stimulates barrier function of cultured endothelial cell monolayer. J Cell Physiol. 1995, 163: 393-399. 10.1002/jcp.1041630219.
Ulfhammer E, Larsson P, Karlsson L, Hrafnkelsdottir T, Bokarewa M, Tarkowski A, Jern S: TNF-alpha mediated suppression of tissue type plasminogen activator expression in vascular endothelial cells is NF-kappaB- and p38 MAPK-dependent. J Thromb Haemost. 2006, 4: 1781-1789. 10.1111/j.1538-7836.2006.02035.x.
Xu H, Ye X, Steinberg H, Liu SF: Selective blockade of endothelial NF-kappaB pathway differentially affects systemic inflammation and multiple organ dysfunction and injury in septic mice. J Pathol. 2010, 220: 490-498.
Ding J, Song D, Ye X, Liu SF: A pivotal role of endothelial-specific NF-kappaB signaling in the pathogenesis of septic shock and septic vascular dysfunction. J Immunol. 2009, 183: 4031-4038. 10.4049/jimmunol.0900105.
Bowie A, O’Neill LA: Vitamin C inhibits NF kappa B activation in endothelial cells. Biochem Soc Trans. 1997, 25: 131S-
Carcamo JM, Pedraza A, Borquez-Ojeda O, Golde DW: Vitamin C suppresses TNF alpha-induced NF kappa B activation by inhibiting I kappa B alpha phosphorylation. Biochemistry. 2002, 41: 12995-13002. 10.1021/bi0263210.
Bowie AG, O’Neill LA: Vitamin C inhibits NF-kappa B activation by TNF via the activation of p38 mitogen-activated protein kinase. J Immunol. 2000, 165: 7180-7188. 10.4049/jimmunol.165.12.7180.
Rodriguez-Porcel M, Lerman LO, Holmes DR, Richardson D, Napoli C, Lerman A: Chronic antioxidant supplementation attenuates nuclear factor-kappa B activation and preserves endothelial function in hypercholesterolemic pigs. Cardiovasc Res. 2002, 53: 1010-1018. 10.1016/S0008-6363(01)00535-1.
Chade AR, Rodriguez-Porcel M, Herrmann J, Zhu X, Grande JP, Napoli C, Lerman A, Lerman LO: Antioxidant intervention blunts renal injury in experimental renovascular disease. J Am Soc Nephrol. 2004, 15: 958-966. 10.1097/01.ASN.0000117774.83396.E9.
Gaut JP, Belaaouaj A, Byun J, Roberts LJ, Maeda N, Frei B, Heinecke JW: Vitamin C fails to protect amino acids and lipids from oxidation during acute inflammation. Free Radic Biol Med. 2006, 40: 1494-1501. 10.1016/j.freeradbiomed.2005.12.013.
Tyml K, Li F, Wilson JX: Septic impairment of capillary blood flow requires nicotinamide adenine dinucleotide phosphate oxidase but not nitric oxide synthase and is rapidly reversed by ascorbate through an endothelial nitric oxide synthase-dependent mechanism. Crit Care Med. 2008, 36: 2355-2362. 10.1097/CCM.0b013e31818024f6.
Shen KP, Lo YC, Yang RC, Liu HW, Chen IJ, Wu BN: Antioxidant eugenosedin-A protects against lipopolysaccharide-induced hypotension, hyperglycaemia and cytokine immunoreactivity in rats and mice. J Pharm Pharmacol. 2005, 57: 117-125. 10.1211/0022357055137.
Tyml K, Li F, Wilson JX: Delayed ascorbate bolus protects against maldistribution of microvascular blood flow in septic rat skeletal muscle. Crit Care Med. 2005, 33: 1823-1828. 10.1097/01.CCM.0000172548.34622.DE.
Wu F, Tyml K, Wilson JX: Ascorbate inhibits iNOS expression in endotoxin- and IFN gamma-stimulated rat skeletal muscle endothelial cells. FEBS Lett. 2002, 520: 122-126. 10.1016/S0014-5793(02)02804-1.
Wu F, Wilson JX, Tyml K: Ascorbate inhibits iNOS expression and preserves vasoconstrictor responsiveness in skeletal muscle of septic mice. Am J Physiol Regul Integr Comp Physiol. 2003, 285: R50-R56.
Wu F, Wilson JX, Tyml K: Ascorbate protects against impaired arteriolar constriction in sepsis by inhibiting inducible nitric oxide synthase expression. Free Radic Biol Med. 2004, 37: 1282-1289. 10.1016/j.freeradbiomed.2004.06.025.
Crimi E, Liguori A, Condorelli M, Cioffi M, Astuto M, Bontempo P, Pignalosa O, Vietri MT, Molinari AM, Sica V, Della Corte F, Napoli C: The beneficial effects of antioxidant supplementation in enteral feeding in critically ill patients: a prospective, randomized, double-blind, placebo-controlled trial. Anesth Analg. 2004, 99: 857-863. 10.1213/01.ANE.0000133144.60584.F6. table of contents
Nathens AB, Neff MJ, Jurkovich GJ, Klotz P, Farver K, Ruzinski JT, Radella F, Garcia I, Maier RV: Randomized, prospective trial of antioxidant supplementation in critically ill surgical patients. Ann Surg. 2002, 236: 814-822. 10.1097/00000658-200212000-00014.
Tanaka H, Matsuda T, Miyagantani Y, Yukioka T, Matsuda H, Shimazaki S: Reduction of resuscitation fluid volumes in severely burned patients using ascorbic acid administration: a randomized, prospective study. Arch Surg. 2000, 135: 326-331. 10.1001/archsurg.135.3.326.
Stephenson C: Author. Study of High-Dose Intravenous Vitamin C Treatment in Patients With Solid Tumors. ClinicalTrials.gov [Ineternet]. 2000, Bethesda (MD): National Library of Medicine (US), NML Identifier: NCT00441207
Copenhagen University Hospital at Herlev: Vitamin C as an Anti-cancer Drug. ClinicalTrials.gov [Ineternet]. 2010, Bethesda (MD): National Library of Medicine (US), NML Identifier: NCT01080352
Thomas Jefferson University: Pilot Trial of Vitamin C in Refractory Non- Dodgkin Lymphoma (NHL). ClinicalTrials.gov [Ineternet]. 2008, Bethesda (MD): National Library of Medicine (US), NML Identifier: NCT00626444
Situs Cancer Research Center: Study of High Dose Intravenous (IV) Ascorbic Acid in Measurable Solid Tumor Disease. ClinicalTrials.gov [Ineternet]. 2008, Bethesda (MD): National Library of Medicine (US), NML Identifier: NCT01125449
Jewish General Hospital: Trial of Chemotherepy Plus Intravenous Vitamin C in Patients With Advanced Cancer for Whom Chemotherepy Alone is Only Marginally Effective. ClinicalTrials.gov [Ineternet]. 2008, Bethesda (MD): National Library of Medicine (US), NML Identifier: NCT01050621
Thomas Jefferson University: Intravenous Vitamin C in Combination With Standard Chemotherepy for Pancreatic Cancer. ClinicalTrials.gov [Ineternet]. 2009, Bethesda (MD): National Library of Medicine (US), NML Identifier: NCT0094525
Ichim TE, Minev B, Braciak T, Luna B, Hunninghake R, Mikirova NA, Jackson JA, Gonzalez MJ, JR M -M, Alexandrescu DT, Dasanu CA, Bogin V, Ancans J, Stevens RB, Markosian B, Koropatnick J, Chen C, Riordan NH: Intravenous ascorbic acid to prevent and treat cancer associated sepsis JTM Editorial 9. 2011
This work in this publication was funded by Batu Biologics.
The authors declare that they have no competing interests.
SCW, BM, NA, BRD, AJK, DTA, CAD, BM, JK, FMM, NHR all contributed to the development of the concept, literature review, discussions, and writing of the manuscript. All authors have read the manuscript and agree to its submission. All authors read and approved the final manuscript.
Samuel C Wagner, Boris Markosian contributed equally to this work.