Autoimmune diseases mediated by a type of white blood cell—T lymphocytes—are currently treated using mainly broad-spectrum immunosuppressants that can lead to adverse side effects. Antioxidants represent an alternative approach for therapy of autoimmune disorders; however, dietary antioxidants are insufficient to play this role. Antioxidant carbon nanoparticles scavenge reactive oxygen species (ROS) with higher efficacy than dietary and endogenous antioxidants. Furthermore, the affinity of carbon nanoparticles for specific cell types represents an emerging tactic for cell-targeted therapy. Here, we report that nontoxic poly(ethylene glycol)-functionalized hydrophilic carbon clusters (PEG-HCCs), known scavengers of the ROS superoxide (O2•−) and hydroxyl radical, are preferentially internalized by T lymphocytes over other splenic immune cells. We use this selectivity to inhibit T cell activation without affecting major functions of macrophages, antigen-presenting cells that are crucial for T cell activation. We also demonstrate the in vivo effectiveness of PEG-HCCs in reducing T lymphocyte-mediated inflammation in delayed-type hypersensitivity and in experimental autoimmune encephalomyelitis, an animal model of multiple sclerosis. Our results suggest the preferential targeting of PEG-HCCs to T lymphocytes as a novel approach for T lymphocyte immunomodulation in autoimmune diseases without affecting other immune cells.
Autoimmune diseases are characterized by loss of tolerance of the immune system for auto-antigens and the subsequent damage to the body caused by its own immune cells. One type of immune cell, T lymphocytes, are important participants in the pathogenesis of a large number of autoimmune diseases1. While the etiology of autoimmunity is not fully understood, a variety of factors including genetic susceptibility and environment triggers, such as infections, can lead to the loss of self-tolerance by T cells and consequently their ability to distinguish self from non-self, causing these cells to target one’s own organs and tissues2. Multiple sclerosis (MS) is a classic example of one of the many tissue-specific chronic T cell-mediated autoimmune diseases. In MS, T cells are thought in many instances to be targeting myelin—the insulating cover of neurons in the brain and spinal cord—leading to neurodegeneration, a wide range of physical and mental symptoms and shortened life span3. Many current therapeutics for autoimmune diseases function as broad-spectrum immunosuppressants that target a variety of immune cells or other mediators of inflammation. They share a common trait: the potential to induce a wide range of serious side effects including increased risk of life-threatening infections and cancer4,5.
Excessive production of reactive oxygen species (ROS) has been implicated in the pathogenesis of multiple T cell-mediated autoimmune diseases4,6,7,8,9. Indeed, the significance of ROS as a therapeutic target for MS has been highlighted with dimethyl fumarate, an approved therapeutic for this disease10. Dimethyl fumarate was first tested for efficacy in MS because of its ability to activate the nuclear factor E2-related factor 2 (Nrf2), a leucine zipper transcription factor, which in turn induces the transcription of antioxidant response element-driven genes and the production of an array of detoxifying antioxidant proteins10,11. While dimethyl fumarate is beneficial in MS, it induces the apoptosis of activated T cells, leading to deleterious lymphopenia and potent and broad immunosuppression in all immune cells12. In addition, Nrf2 levels decrease with age, suggesting a potential loss of Nrf2-mediated efficacy of dimethyl fumarate in older patients13. Finally, studies in Nrf2−/− mice demonstrated that dimethyl fumarate affects immune cell functions in a Nrf2-independent manner14.
Endogenous and dietary antioxidants, such as vitamins C and E, have shown only modest clinical efficacy in autoimmunity6,8, likely due to their poor selectivity for radical annihilation, limited stoichiometric capacity and dependence on detoxifying molecules15. Thus, these are not promising candidates for therapeutic intervention for autoimmune diseases. Moreover, antioxidant dietary supplements require the administration of high doses, which increases mortality, likely due to their indiscriminate effects on all ROS16. A more targeted approach to modulating specific ROS involved in the pathogenesis of autoimmune diseases is likely to display benefits with fewer side effects. Interestingly, low levels of intracellular, but not extracellular, superoxide radicals (O2•−), which are ROS produced by the mitochondria in response to T cell receptor engagement during T cell activation, act as a crucial second messenger during T lymphocyte activation17,18,19,20,21. Since most current therapies for autoimmune diseases are broad-spectrum immunosuppressants associated with deleterious side effects4,5, intracellular O2•− represents an attractive target for modulating T cell activity.
Functionalized carbon nanomaterials, such as fullerenes, single-walled and multiwalled carbon nanotubes, exhibit antioxidant properties superior to those of dietary antioxidants and have been used in a wide range of medical applications including preclinical studies of inflammatory arthritis and neurodegenerative diseases15,22. Carbon nanomaterials have also demonstrated remarkable affinity towards particular cell types and consequently have been used as shuttles for targeted drug delivery23. A major challenge precluding the translation of carbon nanomaterials into the clinic has been their associated cellular toxicity24. However, nanomaterials that are hydrophilic, have no trace metals and that do not form fibrous aggregates, are associated with little to no toxicity15. One such example is poly(ethylene glycol)-functionalized hydrophilic carbon clusters (PEG-HCCs), which have been used as both as a nanovector25 and as an antioxidant in the context of traumatic brain injury15. Indeed, high doses of PEG-HCCs have induced no acute toxicity involving the heart, liver, kidney, spleen or brain in extended mouse studies25. In addition, PEG-HCCs possess clear benefits over currently available antioxidants by specifically and more effectively scavenging O2•− and its derivative, hydroxyl radical15,23,25,26. Interestingly, PEG-HCCs accumulate in the spleen of rodents25, a secondary lymphoid organ. Consequently, here, we determined the ability of splenic immune cells to internalize PEG-HCCs and the ability of the nanoparticles to alter immune cell function and inflammation, ex vivo and in vivo.
PEG-HCCs are preferentially internalized by T lymphocytes over other splenic immune cells
As PEG-HCCs were detectable in the spleens of rodents following systemic administration25, we investigated whether splenic immune cells internalize PEG-HCCs in vivo. We first verified that PEG-HCCs contain acceptably low levels27 of endotoxins (Supplementary Table S1). We then determined their pharmacokinetics in rats by performing an enzyme-linked immunosorbent assay (ELISA) on serum samples collected after a single subcutaneous injection of 2 mg/kg in the scruff of the neck, a dose previously shown effective in rat studies of traumatic brain injury15. Maximum circulating levels of PEG-HCCs (0.6 μg/mL) were reached 24 h after injection (Fig. 1a), likely due to the formation of a subcutaneous slow-release depot, previously observed with other hydrophilic compounds28. The circulating half-life following this peak was 27 h, higher than previously reported after intravenous delivery of PEG-HCCs25, again likely due to a slow release of the nanoparticles from the site of injection28. These data demonstrate subcutaneous bioavailability and sufficient circulating levels of PEG-HCCs for in vivo use in rats. Based on our pharmacokinetic results, we injected rats subcutaneously with 2 mg/kg PEG-HCCs; 24 h later, at the peak of circulation levels, we prepared single-cell suspensions from the spleen, thymus and inguinal lymph nodes draining the injection site (Supplementary Fig. S1). Cells were then washed, labeled with antibodies to cell surface markers of immune cells, fixed and incubated with anti-PEG antibodies to detect the nanoparticles by multi-parametric flow cytometry (FCM) (Supplementary Figs S1 and S2). Cells were either left intact before anti-PEG staining to detect PEG-HCCs at the cell surface, or they were permeabilized before addition of the anti-PEG antibodies to detect PEG-HCCs both at the cell surface and inside the cells (Supplementary Fig. S1). We obtained a stronger signal from the anti-PEG antibodies after permeabilization of splenic T lymphocytes (Fig. 1b, left), demonstrating internalization of the nanoparticles by these cells. In contrast, macrophages, neutrophils, B lymphocytes and natural killer lymphocytes in the spleen showed no difference in PEG-HCCs staining whether the cells were permeabilized or not prior to incubation with anti-PEG antibodies, showing that these immune cells do not internalize PEG-HCCs. No internalization of PEG-HCCs was detected in dendritic cells but the sample size for this population was relatively low in rat splenic preparations compared to the other cell types analyzed (Supplementary Fig. S2b). This result demonstrates that in vivo, PEG-HCCs are preferentially internalized by T cells over other splenic immune cells. This is in sharp contrast to results obtained with other nanoparticles that are internalized by phagocytic cells, such as macrophages or dendritic cells, rather than lymphocytes29,30,31,32. Data were confirmed in the spleen by immunohistochemistry using paraffin-embedded sections from spleens collected 24 h after subcutaneous administration of PEG-HCCs and double-stained for CD3, a marker of T cells and PEG (Supplementary Fig. S3). PEG-HCCs were not internalized by immune cells in the inguinal lymph nodes (Fig. 1b, right), although they could be observed in the intact tissue (Supplementary Fig. S4), suggesting PEG-HCCs may not remain in the lymph nodes sufficiently long enough to be internalized by T cells, unlike in the spleen, a known site of PEG-HCC accumulation25. Interestingly, India ink (carbon black), which has been used extensively as a tracer for lymphatics, also flows through lymph nodes. By histology, India ink is only detected in the lymphatics and inside macrophages in the lymph nodes of rodents, not in the B or T lymphocyte zones33. Our data suggest that PEG-HCCs follow a similar path through lymphatics after subcutaneous injection but are not internalized by macrophages and are not in contact long enough with T lymphocytes for detectable internalization. Furthermore, PEG-HCCs could not be detected in the thymus, an organ crucial for T lymphocyte maturation, suggesting that T cell maturation will not be affected by the nanoparticles. We next determined whether this in vivo selectivity of PEG-HCCs for T lymphocytes over other splenic immune cells is maintained ex vivo. Based on the maximal levels reached in rat serum by the nanoparticles after a single injection of 2 mg/kg, we incubated rat splenocytes ex vivo with 0.1 μg/mL PEG-HCCs and found that, similar to our in vivo findings, the nanoparticles were detectable inside T cells but not other splenic immune cells (Fig. 1c).
To demonstrate the reliability of our FCM technique for PEG-HCC detection, we used thermogravimetric analysis to show that the PEG moieties remain attached to HCCs in the incubation conditions used in our assays (Supplementary Fig. S5). In addition, we performed the flow cytometric analysis with splenocytes incubated in the absence of PEG-HCCs or labeled with secondary antibodies in the absence of primary anti-PEG antibodies, showing minimal positive staining and therefore verifying selectivity of the detection (Supplementary Fig. S6). Similarly, a PEG signal was not detected in spleen sections from rats that had received vehicle instead of PEG-HCCs (Supplementary Fig. S3). Finally, nanoparticles were not detectable in dead T cells, which are readily permeable, thus precluding a non-specific uptake mechanism (Supplementary Fig. S7).
Kinetics of PEG-HCC entry and exit from T cells
To determine if PEG-HCCs enter T cells via active processes, we incubated cells at 4 °C or with sodium azide and found that both conditions attenuated nanoparticle internalization. Chlorpromazine, an inhibitor of clathrin-mediated endocytosis abrogated PEG-HCC internalization, unlike filipin II, an inhibitor of caveolin-mediated endocytosis, thus demonstrating that T lymphocytes internalize PEG-HCCs via clathrin-mediated endocytosis (Fig. 2a). Next, we examined the kinetics of PEG-HCC uptake by T lymphocytes and found maximal intracellular levels after a 25 min incubation at 37 °C; increasing incubation time did not further increase internalization levels (Fig. 2b and Supplementary Fig. S8). We then used transmission electron microscopy to probe the subcellular localization of PEG-HCCs (0.1 μg/mL) in T cells and observed bundles of the nanoparticles in mitochondria. At higher doses (10 μg/mL), PEG-HCCs were also visualized at the cell membrane (Fig. 2c and larger images in Supplementary Fig. S9).
Accumulation of nanomaterials in cells would increase the risk for toxicity; we therefore assessed the ability of T cells to release or degrade the PEG-HCCs. When T lymphocytes were incubated with PEG-HCCs for 30 min to allow internalization, washed and maintained in media at 37 °C, both external and internal levels of PEG-HCCs decreased over 6 h (Fig. 2d and Supplementary Fig. S8), demonstrating that the nanoparticles do not accumulate inside the T cells over time. To determine whether this loss in detection is due to rapid degradation or exit from the cells, we performed a cell-based sandwich ELISA (Supplementary Fig. S10). In the absence of cells, PEG-HCCs were readily detected and saturated the detection signal (Fig. 2e). When T lymphocytes loaded with increasing concentrations of PEG-HCCs were placed onto the antibody-coated plate for 5 h, PEG-HCCs were detected in a dose-dependent manner, indicating that PEG-HCCs exit the T lymphocytes. Importantly, unconjugated mPEG-NH2 (5000 kDa) alone was not detected by the assay, providing further confirmation that the anti-PEG antibodies used throughout this study can only detect conjugated PEG moieties as claimed by its manufacturer.
PEG-HCC internalization is not biased towards major T cell subsets
Since PEG-HCCS are not internalized by all T cells, we used FCM to determine whether the nanoparticles are preferentially targeted to specific T lymphocyte subsets. We began our analysis with two major subpopulations of T cells: naïve (CD62L+) and memory (CD62L−) T cells (Fig. 3a) and helper (CD4+) and cytotoxic (CD8+) T cells (Fig. 3b); all of which internalize PEG-HCCs to a similar extent. Next, we determined whether PEG-HCCs distinguish between resting T cells and T cells activated with a mitogen; T lymphocyte activation improved nanoparticle uptake, although resting T lymphocytes could internalize them too (Fig. 3b). As our data had indicated that PEG-HCCs entered approximately 5–10% of T cells, we investigated T cell subsets present at a lower frequency in the spleen. We first analyzed δγ T cells that represent a small fraction of all T cells and also which play a role in autoimmunity34, but found no difference between these and other T cells in terms of PEG-HCC internalization (Fig. 3c). Additionally, we studied primary T helper 1 (TH1)-polarized effector memory T cells, a population implicated in some autoimmune diseases35 and found that PEG-HCCs were also internalized by these cells to a similar extent as other T cells (Fig. 3d). Taken together, these findings suggest that, while PEG-HCCs are preferentially internalized by T cells over other splenic immune cells, they do not target a specific subset of T cells.
PEG-HCCs inhibit the activation of rat and human T lymphocytes
We assessed the consequences of PEG-HCC internalization on ex vivo T cell activity. PEG-HCCs induced a reduction in both intracellular O2•− levels and proliferation of antigen-stimulated ovalbumin-specific or myelin basic protein-specific primary rat CD4+ T cells (Fig. 4a,b and Supplementary Fig. S11)36,37,38. Human peripheral blood T cells or rat splenic T cells (Supplementary Fig. S12) stimulated with mitogens were similarly sensitive to PEG-HCCs. In contrast, mPEG-NH2 (5000 kDa), used alone as a control, did not affect T cell proliferation (Supplementary Fig. S13), whereas non-PEGylated HCCs did inhibit proliferation (Supplementary Fig. S11). However, unlike PEG-HCCs, HCCs flocculate rapidly in water (Supplementary Fig. S11), precluding their in vivo use.
Washing away excess PEG-HCCs and then immediately stimulating the rat T cells did not alter their effect on proliferation (Fig. 4c). In contrast, stimulating the T cells 6 h after washout rescued the inhibitory effect on proliferation (Fig. 4c), demonstrating that the nanoparticles need to be internalized to decrease T lymphocyte activity. This result is in alignment with the kinetics shown in Fig. 2d and suggests that PEG-HCCs exert a reversible effect on T cell activity. We also compared the efficacy of PEG-HCCs with that of vitamin C and trolox (water-soluble analog of vitamin E) and found that these two well-characterized antioxidants had no effect on T lymphocyte proliferation (Fig. 4d), suggesting the higher antioxidant capacity of PEG-HCCs26 is necessary for this inhibitory effect. Finally, we used FCM to examine the effects of PEG-HCCs on the production of proinflammatory cytokines involved in autoimmune diseases, such as MS, by antigen- or mitogen- stimulated T cells and found a ~30% reduction in the intracellular levels of the TH1 cytokines interleukin (IL)-2 and interferon (IFN)-γ, but no effect on expression levels of the TH17 cytokine IL-17A (Fig. 4e and Supplementary Fig. S14), suggesting distinct cell signaling pathways are altered by PEG-HCCs.
Dimethyl fumarate induces the apoptosis of activated T cells12. To determine whether the observed effects of PEG-HCCs on T cell proliferation and cytokine production were due to nanoparticle cytotoxicity, we used FCM to analyze cell death in ovalbumin-specific and myelin basic protein-specific rat T cells incubated with PEG-HCCs or HCCs prior to stimulation and found no changes in cell viability (Fig. 4f and Supplementary Fig. S11). In addition, treating unstimulated T cells with PEG-HCCs did not affect their basal homeostatic proliferation in the absence of antigen or exogenous cytokines (Supplementary Fig. S15), suggesting that an increase in intracellular O2•− levels during T lymphocyte activation17,18,19,20,21 is necessary for PEG-HCCs to alter cellular function.
PEG-HCCs leave key functions of macrophages unaltered
We demonstrated in Fig. 1 that macrophages do not internalize PEG-HCCs in vivo or ex vivo. However, because macrophages critically regulate T cell function through a variety of mechanisms, including chemoattractant production, phagocytosis and antigen processing and presentation, we determined whether PEG-HCCs influenced any of these macrophage activities. We stimulated primary rat splenic macrophages with lipopolysaccharide (LPS) to induce the secretion of T lymphocyte chemoattractants, as measured by the ability of macrophage culture supernatants to induce T cell migration through transwell membranes. Adding PEG-HCCs during macrophage stimulation did not affect T lymphocyte migration (Fig. 5a), demonstrating that the nanoparticles do not alter the production of T cell chemoattractants by macrophages. Additionally, incubating unstimulated T lymphocytes with PEG-HCCs did not alter their migration (Fig. 5a), in agreement with our finding that PEG-HCCs do not affect unstimulated T cells. We further found that, unlike other nanoparticles39, PEG-HCCs do not affect phagocytosis by macrophages (Fig. 5b and Supplementary Fig. S16). To measure antigen processing and presentation, macrophages were loaded with ovalbumin, washed and provided ovalbumin-specific T cells; T cell proliferation was used to assess adequate antigen processing and presentation (Supplementary Fig. S17). T cell proliferation was unaffected when PEG-HCCs were added to macrophages upon ovalbumin-loading, demonstrating a lack of effects of PEG-HCCs on antigen processing and presentation by macrophages (Fig. 5c). However, the addition of PEG-HCCs to macrophages at the same time as the T cells led to a reduction in T cell proliferation (Fig. 5c), similar to our findings in Fig. 4b.
In addition to their role as antigen-presenting cells, macrophages play a central part in pathogen defense. We therefore tested the effects of PEG-HCCs on the ability of macrophages to prevent the growth of the fungus Aspergillus niger and found no fungistatic effects (Fig. 5d). As a control, we verified that PEG-HCCs alone do not induce fungistasis (Supplementary Fig. S18). These results indicate that PEG-HCCs do not alter major functions of macrophages, likely as a result of the inability of these cells to internalize the nanoparticles.
PEG-HCCs are effective in reducing memory T lymphocyte reactions in vivo
The intriguing preferential immunomodulatory properties of PEG-HCCs on T lymphocytes over other splenic immune cells encouraged us to examine their effects in T lymphocyte-mediated inflammation. We chose delayed-type hypersensitivity (DTH), also known as type IV hypersensitivity, as a first model as it is a well-characterized model of inflammation mediated by memory T lymphocytes that have had previous encounter with their antigen. We elicited an active DTH response against ovalbumin in rats40 and found that a single subcutaneous injection of 2 mg/kg PEG-HCCs, at either time of immunization or challenge, was sufficient to decrease inflammation (Fig. 6a). A similar result was obtained in the adoptive model of DTH elicited by the injection of antigen-stimulated GFP-transduced ovalbumin-specific T cells, followed by ovalbumin challenge (Fig. 6b)38,41. Detection of the GFP-transduced ovalbumin-specific T cells by FCM at the site of inflammation showed no difference in homing of the T cells after vehicle or PEG-HCC treatment (Fig. 6b). This result suggests that the effects of PEG-HCCs on DTH are due to impaired T cell reactivation in situ, as found with some T lymphocyte-directed immunomodulators38, rather than homing inhibition as seen with other T cell immunomodulators42.
These beneficial effects of PEG-HCCs on active and adoptive DTH prompted us to test the effects of PEG-HCCs in rats with active acute experimental autoimmune encephalomyelitis (EAE), a model of MS. Subcutaneous treatment with 2 mg/kg PEG-HCCs every three days (equivalent to three circulating half-lives based on our pharmacokinetics data), starting after the onset of clinical signs, reduced disease severity (Fig. 6c, Supplementary Movie S1 and Movie S2). Histologic analysis of spinal cords collected from EAE rats at peak of disease (day 12 post-immunization) revealed a decrease in inflammatory foci (Fig. 6d), suggesting that PEG-HCCs reduce immune cell infiltration into the central nervous system.
In summary, we have demonstrated that the antioxidant carbon nanoparticles, PEG-HCCs, are immunomodulators that preferentially target T lymphocytes. We established that, unlike other nanoparticles that mainly target phagocytic cells17,18,19,20,21, PEG-HCCs are preferentially internalized by T lymphocytes over other immune cells. While we were not able to identify a single mechanism responsible for this preferential uptake, our data indicate that PEG-HCCs enter the cells mainly via clathrin-mediated endocytosis, similar to other carbon nanoparticles43. We took advantage of the unique property of PEG-HCCs to favor T cells to demonstrate that PEG-HCCs scavenge intracellular O2•− produced via antigen-stimulation of T cells and, consequently, reversibly inhibit proliferation and the production of proinflammatory cytokines without cytotoxicity. Our findings are in line with studies demonstrating the use of antioxidants to attenuate T cell activation induced by mitogens or antigens21. We established that the inhibition of T cell activity by PEG-HCCs was not due to an extraneous effect on chemoattraction, phagocytosis, or antigen processing and presentation by macrophages, which are essential steps utilized by antigen-presenting cells for the physiological activation of T cells44.
A major implication of these data is that the inability to internalize PEG-HCCs allows key immune functions of macrophages to remain unaltered. This demonstrates that PEG-HCCs are selective for some immune cells and suggests that pathogen defense by macrophages remains intact. However, additional work is required to elucidate the effects of PEG-HCCs on T lymphocyte subpopulations that help to maintain self-tolerance such as regulatory T cells45. Furthermore, future studies will be necessary to determine if PEG-HCCs affect the use of O2•− as a microbicidal agent by neutrophils46. However, the significance of our ex vivo results on T cell activity by PEG-HCCs was clearly demonstrated by the findings that administration of these nanoparticles into rat models led to a reduction in DTH response, immune infiltration into the spinal cord and EAE scores. Together, these data suggest that PEG-HCCs are attractive new tools for treating T cell-mediated autoimmune diseases.
Female inbred Lewis rats were purchased from Charles River and group-housed in autoclaved cages with irradiated rodent chow and water ad libitum in a facility approved by the American Association for Laboratory Animal Science. Thymus donors were 38–42 days old. All remaining studies used rats aged 43–48 days old. All procedures were in accordance with National Institutes of Health guidelines and approved by the Institutional Animal Care and Use Committee at Baylor College of Medicine. Animals were euthanized following guidelines from the American Veterinary Medical Association.
Splenocytes were isolated from spleens of naïve rats47. Mononuclear splenocytes were isolated using Histopaque-1077 (Sigma-Aldrich)48. Human peripheral blood cells were isolated from buffy coats (Gulf Coast Regional Blood Center, Houston, TX). Primary Lewis rat GFP-transduced ovalbumin-specific T cells were a kind gift from Alexander Flügel (Munich, Germany)37. Primary Lewis rat myelin basic protein-specific T cells were a kind gift from Evelyne Béraud (Université de la Méditerranée, Marseilles, France)36. As antigen-presenting cells for ovalbumin-specific or myelin-basic protein-specific T cell stimulation, either rat splenic macrophages or irradiated (30 Gy) rat thymocytes were used47. Lymph node cells were isolated from inguinal lymph nodes of rats with EAE at the peak of disease (day 12 post-immunization) by preparing a single-cell suspension using 70 μm cell strainers. Cells were cultured as described49 unless specified otherwise.
For all experiments, PEG-HCCs and HCCs were prepared as described25. The materials were purified by size using crossflow (tangential) filtration. All samples were sterile-filtered before storage and further use. The starting source of carbon has remained unchanged since the first publication on PEG-HCCs25. PEG-HCCs are stable for >5 months in solution at neutral pH. Acid (pH < 2) will cause amide bond cleavage over long times at room temperature and base (pH > 10) will cause further fragmentation of HCCs over time. However, there are no changes in Raman, IR or XPS over months in neutral water50. Endotoxin levels in PEG-HCCs were measured using ToxinSensor Chromogenic LAL Endotoxin Assay Kit (GenScript) using the manufacturer’s protocol.
Blood was drawn51 at various time points after a single subcutaneous injection of 2 mg/kg body weight of PEG-HCCs in the scruff of the neck. Serum levels of PEG-HCCs were quantitated using a PEGylated protein ELISA kit (Enzo Life Sciences). Circulating half-life was determined by fitting the data to a single exponential decay.
Cells were washed with ice-cold FCM buffer (PBS + 2% goat serum + 2% BSA), stained with antibodies (Table S2) and fixed with ice-cold PBS + 1% paraformaldehyde. Data were acquired on a FACSCanto II or LSRFortessa (Becton Dickinson) with the FACSDiva software within the Cytometry and Cell Sorting core at Baylor College of Medicine and analyzed using FlowJo software (Treestar). For each sample, doublet discrimination was performed and 30,000 events were acquired.
Cellular uptake of PEG-HCCs
Freshly isolated rat splenocytes were resuspended (1 × 106 cells/mL) in medium + 5% FBS and incubated with or without PEG-HCCs (0.1 μg/mL) for the indicated times at 37 °C, 5% CO2 unless indicated in the figure caption. Cells were then washed with FCM buffer and incubated with purified mouse IgG (Life Technologies) to block FcγII/FcγIII receptors. Cells were stained with antibodies (Table S2) directed against surface markers, washed and fixed. Cells were either left intact or permeabilized with freshly prepared 0.5% saponin (EMD Millipore) in FCM buffer and then stained for PEG-HCCs with an anti-PEG antibody and analyzed by FCM (Supplementary Figs S1 and S2). Saponin was selected as the detergent as Tween-20 and Triton X-100 contain PEG and can produce false positive signals. 25 mM sodium azide (Sigma-Aldrich) was used to inhibit active transport processes; 1 μg/mL filipin III (Cayman Chemical) was used to block caveolin-mediated endocytosis; 10 μg/mL chlorpromazine (Sigma-Aldrich) was used to inhibit clathrin-mediated endocytosis52. Background signal from the anti-PEG antibody in the absence of PEG-HCCs was subtracted during analysis.
Rats were injected with 2 mg/kg PEG-HCCs subcutaneously, humanely euthanized after 24 h and paraffin-embedded spleen sections were prepared. Sections were dewaxed with xylene (Fisher), hydrated through a gradient of ethanol and washed in PBS. Antigen-recovery was performed using pre-heated sodium citrate buffer (10 mM, pH 6.5) for 15 min in microwave. Sections were cooled to room temperature and non-specific staining was prevented by incubating sections overnight in PBS + 5% goat serum + 5% BSA. Sections were incubated with anti-CD3 and anti-PEG antibodies for 2 h at room temperature, washed with PBS and incubated with secondary conjugate antibodies for 1 h at room temperature. Sections were then washed and dehydrated in 100% ethanol through a gradient, soaked with xylene and mounted with SlowFade mountant with DAPI. Representative photos were taken at 10× magnification on an Olympus IX71 epifluorescence microscope equipped with an Olympus Qcolor 5 camera and the SimplePCI software, v.6.6.0.053.
Two mL of 1 mg/mL PEG-HCCs were incubated for 0, 1 and 24 h at 37 °C with 2 mL of fresh Lewis rat serum passed through a 100,000 MWCO filter (Amicon Ultra-4 Centrifugal Filter Unit). PEG-HCCs were isolated from serum by filtration through a second 100,000 MWCO filter and washed with 4 mL of deionized water three times. Remaining water was removed from PEG-HCCs by evaporation under reduced pressure and analyzed by thermogravimetric analysis (TA Instruments Q-600 Simultaneous TGA/DSC) to determine the mass percentages of PEG in the PEG-HCCs.
Transmission electron microscopy
Ovalbumin-specific rat T cells (2 × 106 cells) were resuspended in medium + 5% FBS and incubated with or without PEG-HCCs (0.1 or 10 μg/mL) for 30 min at 37 °C, 5% CO2. Cells were washed with PBS and pelleted by centrifuge for processing and imaging by the Integrated Microscopy Core at Baylor College of Medicine. Four separate pellets were dispersed in ice-cold modified Karnovsky’s fixative in 0.1 M cacodylate buffer at pH 7.37 for 2.5 hours. The suspension was re-pelleted at 6000 RPM for 10 min, supernatant decanted and cells quenched in 0.4% FSG for 25 min. Pellets remained fixed to the side of 1.5 mL tubes and were processed in the tube for the remainder of the protocol. After 3 × 5 min washes with 0.1 M cacodylate buffer, the pellets were osmicated for 45 min and then held overnight in 0.1 M cacodylate buffer. The following morning, pellets were rinsed in 4 × 5 min ddH2O and dehydrated in 100% ethanol through a gradient series of ethanol. Pellets were gradually infiltrated through a gradient series of plastic-ethanol mixtures and left to infiltrate overnight in 100% plastic without catalyst. This was followed by several changes in pure plastic with catalyst, then pellets were embedded in Spurr Low Viscosity resin and polymerized at 62 °C for 3 days. Ultra-thin sections were cut on a Diatome Ultra45 knife using a Leica U6 ultramicrotome. Sections were collected on 150 hex-mesh copper grids, stained with saturated aqueous uranyl acetate and counter-stained with Reynold’s lead citrate. The stained sections were viewed on a Hitachi H7500 transmission electron microscope and images were captured using an AMT XR-16 digital camera and AMT Image Capture software, v602.600.51.
Measurement of PEG-HCC exit from the T lymphocytes
Immulon 4 HBX flat-bottom 96-well plates were coated with purified anti-PEG antibodies (Table S2, 100 μl, 5 μg/mL) at 4 °C for 24 h. Resting ovalbumin-specific rat T cells were resuspended (1 × 106 cells/mL) in medium + 5% FBS and incubated with or without PEG-HCCs (0.1–100 μg/mL) for 30 min at 37 °C, 5% CO2. Cells were washed thoroughly with medium while the antibody-containing plate was washed with PBS. Cells were seeded into the plate (1 × 105 per well) and incubated for 5 h at 37 °C, 5% CO2. Cells were removed from the plate that was washed thoroughly with PBS. Biotinylated anti-PEG antibodies (Table S2) were added to wells (1 μg/mL) and incubated for 1 h at room temperature. The plate was washed thoroughly with PBS after which streptavidin conjugated to alkaline phosphatase was added to each well (1 μg/mL) and incubated for 20 min at room temperature. The plate was washed thoroughly and 1-step p-nitrophenyl phosphate (PNPP) substrate (ThermoScientific) was added to each well, incubated for 15–30 min at room temperature to allow color development and 2 N sodium hydroxide was added to each well to stop the reaction. Absorbance was measured at 405 nm on a Multiscan EX plate reader (ThermoScientific).
Ovalbumin-specific rat T cells were resuspended in RPMI 1640 medium (1 × 106 cells/mL) without supplements or serum, plated in a 6-well culture dish and loaded with 5 μM dihydroethidium (Life Technologies) for 30 min at 37 °C, 5% CO2. Cells were washed with RPMI 1640 and incubated with or without PEG-HCCs (0.1–100 μg/mL) for 30 min at 37 °C, 5% CO2. Cells were washed with PBS + 1% BSA and stimulated with 50 ng/mL PMA and 1 μg/mL ionomycin (Sigma-Aldrich) for 45 min prior to FCM analysis.
T lymphocyte proliferation
Ovalbumin-specific or myelin basic protein-specific rat T cells were resuspended in medium + 5% FBS and seeded in a 96-well plate (5 × 104 per well) in the presence of irradiated rat thymocytes (2 × 106 per well), serving as antigen-presenting cells38,54,55,56. Rat mononuclear splenocytes and human peripheral blood cells were resuspended in medium + 5% FBS and seeded in a 96-well plate (1 × 105 per well)40,57. Cells were incubated with or without antioxidants: trolox (Sigma-Aldrich), vitamin C (Sigma-Aldrich), PEG-HCCs, or HCCs for 30 min at 37 °C and 5% CO2. Ovalbumin-specific and myelin basic protein-specific rat T cells were stimulated with 10 μg/mL ovalbumin or guinea pig myelin basic protein (Sigma-Aldrich), respectively36,38,58. Rat mononuclear splenocytes and human peripheral blood cells were stimulated with 1 μg/mL concanavalin A or phytohemagglutinin, respectively36,59. Cells were cultured for 72 h at 37 °C and 5% CO2 and 1 μCi [3H] thymidine (MP Biomedicals) was added to each well during the final 16–18 h of incubation. Cells were then lysed by freezing and DNA was harvested on fiberglass filters using a cell harvester (Inotech Biosystems International). [3H] thymidine incorporation was measured on a β-scintillation counter (Beckman Coulter).
Cytokine production by T lymphocytes
Ovalbumin-specific rat T cells and cells isolated from the draining lymph nodes of rats with EAE at peak of disease were resuspended (5 × 104 cells/mL) in medium + 5% FBS and incubated with or without PEG-HCCs (10, 100 μg/mL) for 30 min at 37 °C and 5% CO2. Ovalbumin-specific T cells were stimulated by irradiated rat thymocytes (2 × 106 cells/mL) pre-incubated with 10 μg/mL ovalbumin for 2 h. Lymph node cells were stimulated with 50 ng/mL PMA and 1 μg/mL ionomycin. To inhibit cytokine secretion, 10 μg/mL brefeldin A (eBioscience) was immediately added to all wells. Cells were then cultured 4 h at 37 °C and 5% CO2, fixed and permeabilized with 0.1% Triton X-100 (Sigma-Aldrich). Ovalbumin-specific T cells were stained with anti-IL-2 and anti-IFN-γ antibodies, while lymph node cells were stained with an anti-IL-17A antibody and appropriate secondary antibodies (Supplementary Table S2) and then analyzed by flow cytometry59.
Antigen processing and presentation by macrophages
Freshly isolated rat splenic macrophages were resuspended in medium + 10% FBS, seeded in a 96-well plate (2 × 104 per well), incubated with 10 μg/mL ovalbumin for 2 h to allow cells to adhere and process antigen and then washed with PBS. Ovalbumin-specific rat T cells were resuspended in medium + 10% FBS and added to the macrophages (1 × 104 per well). Macrophages were incubated with or without PEG-HCCs (15–120 μg/mL), for 30 min at 37 °C, 5% CO2, either at the same time as antigen loading or upon addition of T cells (Supplementary Fig. S18). An effect on macrophage antigen processing and presentation by PEG-HCCs was gauged by comparing T cell proliferation against vehicle-treated stimulated cells.
Cytotoxicity in response to PEG-HCCs was measured by FCM60. More details are provided in the Supplementary Information. Ovalbumin-specific and myelin basic protein-specific rat T cells were resuspended (1 × 106 cells/mL) in medium + 5% FBS and incubated with or without PEG-HCCs or HCCs (100 μg/mL) for 30 min at 37 °C and 5% CO2 prior to stimulation with 10 μg/mL ovalbumin and myelin basic protein, respectively. Cells were cultured for 72 h at 37 °C and 5% CO2. Positive control wells received 0.5 μM staurosporine (EMD Millipore) during the last 16 h to induce cell death. Cells were then washed and stained with 7-aminoactinomycin D (Sigma-Aldrich) to detect dead cells and analyzed by FCM.
Macrophage chemokine production and T cell migration
Freshly isolated rat macrophages were resuspended (2 × 106 cells/mL) in medium + 10% FBS and cultured overnight at 37 °C and 5% CO2 to allow macrophages to adhere. Cells were washed with PBS to remove non-adherent cells and incubated with or without PEG-HCCs (15, 120 μg/mL) for 30 min at 37 °C and 5% CO2. Macrophages were then stimulated with 10 ng/mL lipopolysaccharide (LPS)61. After 24 h incubation at 37 °C and 5% CO2, 0.6 mL supernatant was transferred to the bottom chamber of a 5 μm 24-well transwell filter plate (Costar) to serve as chemoattractant. Ovalbumin-specific T cells were resuspended (1 × 106 cells/mL) in serum-free medium, incubated with or without PEG-HCCs (15, 120 μg/mL) for 30 min at 37 °C and 5% CO2 and 2 × 105 cells were seeded in each transwell insert. As an input control, 2 × 105 T cells were placed in the bottom chamber of one well without a transwell insert. The transwell plate was incubated at 37 °C and 5% CO2 for 4 h, prior to counting the bottom chambers for migratory T cells using a hemocytometer. Percent migratory cells was calculated using the following equation: = [(number of cells in bottom chamber)/(number of cells in input control)] × 100. Chemoattractant containing either medium alone, medium + 10% FBS, or supernatant from unstimulated macrophages are shown as controls.
Freshly isolated rat splenocytes (8 × 106 cells/mL) were plated in chamber slides (Lab-Tek) for 2 h to allow macrophages to adhere. Slides were washed with PBS to remove non-adherent cells and remaining macrophages were incubated with or without PEG-HCCs (1–60 μg/mL) for 30 min at 37 °C, 5% CO2. Incubation with iron(II,III) oxide (Fe3O4) nanoparticles (25 μg/mL) served as a control for phagocytosis inhibition39. Alexa Fluor 488-conjugated zymosan A bioparticles (Life Technologies) were then added to macrophages following manufacturer’s instructions. Slides were incubated for 1 h at 37 °C and 5% CO2, fixed and mounted with SlowFade with DAPI (Life Technologies). Representative photos were taken at 10× magnification with an Olympus IX71 epifluorescence microscope. Percent of phagocytizing cells was calculated in eight random fields of view using the following equation: = [(number of macrophages with engulfed bioparticles)/(total number of macrophages)] × 100.
Macrophage fungistatic assay
The ability of splenic macrophages to prevent growth of Aspergillus niger was tested as described62. Splenic macrophages were isolated by adhesion as described above and plated into 24 well plates (0.2 × 106 cells/well) until adherent. Cells were treated with PEG-HCCs and Aspergillus niger (200 conidia/well) were added before a 24 h incubation at 37 °C, 5% CO2 and enumeration of hyphal growth.
Delayed-type hypersensitivity induction and monitoring
For induction of active DTH, rats were immunized in the lower flank using ovalbumin emulsified in complete Freund’s adjuvant (Difco)63. For induction of adoptive DTH, GFP-transduced ovalbumin-specific rat T cells were activated ex vivo by stimulation with 10 μg/mL ovalbumin in the presence of irradiated rat thymocytes, serving as antigen-presenting cells38,54. Cells were incubated 48 h at 37 °C and 5% CO2 and then injected intraperitoneally into rats (1 × 106 T cells/rat). Rats were randomly selected to receive a single subcutaneous injection in the scruff of the neck of saline (vehicle) or PEG-HCCs (2 mg/kg body weight) either at the time of immunization (active DTH only) or at time of challenge. One week after immunization or two days after adoptive transfer, animals were challenged with ovalbumin dissolved in PBS in the pinna of one ear and a sham injection of PBS in the opposite ear38,54. At 48 h post-challenge, ear swelling was measured using a spring-loaded micrometer (Mitutoyo) and the difference in ear thickness was calculated for each animal. Rats with adoptive DTH were humanely euthanized immediately after DTH measurement. After cardiac perfusion with saline, ears were collected and single-cell suspensions were prepared using a 70 μm cell strainer prior to flow cytometry analysis to detect GFP transduced cells at the site of inflammation38.
Acute active EAE induction and histology
EAE was induced by immunizing rats with an emulsion of guinea pig myelin basic protein (Sigma-Aldrich) in complete Freund’s adjuvant supplemented to a final concentration of 4 mg/mL heat-killed Mycobacterium tuberculosis H37Ra (Difco) at the base of the tail. Rats were randomly selected to receive subcutaneous treatment with saline (Vehicle) or PEG-HCCs (2 mg/kg body weight) beginning at onset of clinical signs and continued every three days until the vehicle-treated rats spontaneously recovered. Rats were weighed and scored twice daily using the following scale: 0 – no disease signs; 0.5 – distal limp tail; 1 – fully limp tail; 2 – mild paraparesis; 3 – moderate paraparesis; 3.5 – one hind leg paralyzed; 4 – both hind legs paralyzed; 5 – hind leg paralysis and incontinence; 6 – moribund, requires immediate euthanasia28,38,64.
Randomly selected rats with EAE were humanely euthanized at the peak of disease (day 12 post-immunization). After cardiac perfusion with saline65, spinal columns were removed and fixed in 10% buffered formalin. The lumbar region of the spinal cord was carefully dissected, embedded in paraffin, sectioned and stained with hematoxylin and eosin within the Pathology and Histology facility at Baylor College of Medicine. Slides were scored blindly by two investigators for the degree of immune cell infiltration into the gray matter of the spinal from three randomly selected cross-sections from each animal: 0 – none; 1 – low (1–10%); 2 – moderate (11–50%); 3 – high (51–100%). Representative photos were taken at 40× magnification with an upright Olympus BX41 microscope equipped with a QImaging QICAM Fast1394 camera and the QCapture Pro software v184.108.40.2062.
All data are expressed as means ± standard error of the mean (s.e.m). Parametric statistical methods were utilized to achieve sufficient statistical power with small sample sizes (n < 4); Bonferonni post-hoc tests were used for pairwise comparisons. All remaining analyses utilized non-parametric methods: a two-tailed Mann-Whitney test for comparisons between two groups, a Kruskal-Wallis test and Dunns post-hoc tests for comparisons between three or more groups; EAE data was analyzed using a Wilcoxon matched pairs test. All analyses utilized a significance level of P < 0.05 and were performed using Prism (GraphPad).
How to cite this article: Huq, R. et al. Preferential uptake of antioxidant carbon nanoparticles by T lymphocytes for immunomodulation. Sci. Rep. 6, 33808; doi: 10.1038/srep33808 (2016).
Shapenko, A., Leipe, J., Lipsky, P. E. & Schulze-Koops, H. The role of the T cell in autoimmune inflammation. Arthritis Res. Ther. 7 (Suppl 2), S4 (2005).
Marrack, P., Kappler, J. & Kotzin, B. L. Autoimmune disease: why and where it occurs. Nat. Med. 7, 899–905 (2001).
Legroux, L. & Arbour, N. Multiple sclerosis and T lymphocytes: an entangled story. J. Neuroimmune Pharmacol. 10, 528–546 (2015).
Ontaneda, D., Hyland, M. & Cohen, J. A. Multiple Sclerosis: New Insights in Pathogenesis and Novel Therapeutics. Annu. Rev. Med. 63, 389–404 (2012).
Rosman, Z., Shoenfeld, Y. & Zandman-Goddard, G. Biologic therapy for autoimmune diseases: an update. In BMC Med. 11 88 (2013).
Gilgun-Sherki, Y., Melamed, E. & Offen, D. The role of oxidative stress in the pathogenesis of multiple sclerosis: the need for effective antioxidant therapy. J. Neurol. 251, 261–268 (2004).
Padgett, L. E., Broniowska, K. A., Hansen, P. A., Corbett, J. A. & Tse, H. M. The role of reactive oxygen species and proinflammatory cytokines in type 1 diabetes pathogenesis. Ann. N. Y. Acad. Sci. 1281, 16–35 (2013).
Rosenbaum, C. C., O’Mathuna, D. P., Chavez, M. & Shields, K. Antioxidants and antiinflammatory dietary supplements for osteoarthritis and rheumatoid arthritis. Altern. Ther. Health Med. 16, 32–40 (2010).
van Horssen, J., Witte, M. E., Schreibelt, G. & de Vries, H. E. Radical changes in multiple sclerosis pathogenesis. Biochim. Biophys. Acta 1812, 141–150 (2011).
Kappos, L. et al. Efficacy and safety of oral fumarate in patients with relapsing-remitting multiple sclerosis: a multicentre, randomised, double-blind, placebo-controlled phase IIb study. Lancet 372, 1463–1472 (2008).
Linker, R. A. & Gold, R. Dimethyl fumarate for treatment of multiple sclerosis: mechanism of action, effectiveness and side effects. Curr. Neurol. Neurosci. Rep. 13, 394 (2013).
Gill, A. J. & Kolson, D. L. Dimethyl fumarate modulation of immune and antioxidant responses: application to HIV therapy. Crit. Rev. Immunol. 33, 307–359 (2013).
Rahman, M. M., Sykiotis, G. P., Nishimura, M., Bodmer, R. & Bohmann, D. Declining signal dependence of Nrf2-MafS-regulated gene expression correlates with aging phenotypes. Aging Cell 4, 554–562 (2013).
Schulze-Topphoff, U. et al. Dimethyl fumarate treatment induces adaptive and innate immune modulation independent of Nrf2. Proc. Natl. Acad. Sci. USA 113, 4777–4782 (2016).
Bitner, B. R. et al. Antioxidant carbon particles improve cerebrovascular dysfunction following traumatic brain injury. ACS Nano. 6, 8007–8014 (2012).
Bjelakovic, G., Nikolova, D., Gluud, L. L., Simonetti, R. G. & Gluud, C. Mortality in randomized trials of antioxidant supplements for primary and secondary prevention: systematic review and meta-analysis. JAMA 297, 842–857 (2007).
Belikov, A. V., Schraven, B. & Simeoni, L. TCR-triggered extracellular superoxide production is not required for T-cell activation. Cell. Commun. Signal 12, 50 (2014).
Devadas, S., Zaritsaya, L., Rhee, S. G., Oberley, L. & Williams, M. S. Discrete generation of superoxide and hydrogen peroxide by T cell receptor stimulation: selective regulation of mitogen-activated protein kinase activation and fas ligand expression. J. Exp. Med. 195, 59–70 (2002).
Kaminski, M. M. et al. Mitochondrial reactive oxygen species control T cell activation by regulating IL-2 and IL-4 expression: mechanism of ciprofloxacin-mediated immunosuppression. J. Immunol. 184, 4827–4841 (2010).
Sena, L. A. et al. Mitochondria are required for antigen-specific T cell activation through reactive oxygen species signaling. Immunity 38, 1–12 (2013).
Williams, M. S. & Kwon, J. T cell receptor stimulation, reactive oxygen species and cell signaling. Free Radic. Biol. Med. 37, 1144–1151 (2004).
Yudoh, K., Karasawa, R., Masuko, K. & Kato, T. Water-soluble fullerene (C60) inhibits the development of arthritis in the rat model of arthritis. Int. J. Nanomed. 4, 217–225 (2009).
Marcano, D. C. et al. Design of poly(ethylene glycol)-functionalized hydrophilic carbon clusters for targeted therapy of cerebrovascular dysfunction in mild traumatic brain injury. J. Neurotrauma. 30, 789–796 (2013).
Drezek, R. A. & Tour, J. M. Is nanotechnology too broad to practise? Nat. Nanotechnol. 5, 168–169 (2010).
Berlin, J. M. et al. Effective drug delivery, in vitro and in vivo, by carbon-based nanovectors noncovalently loaded with unmodified Paclitaxel. ACS Nano 4, 4621–4636 (2010).
Samuel, E. L. et al. Highly efficient conversion of superoxide to oxygen using hydrophilic carbon clusters. Proc. Natl. Acad. Sci. USA 112, 2343–2348 (2015).
Malyala, P. & Singh, M. Endotoxin limits in formulations for preclinical research. J. Pharm. Sci. 97, 2041–2044 (2007).
Tarcha, E. J. et al. Durable pharmacological responses from the peptide ShK-186, a specific Kv1.3 channel inhibitor that suppresses T cell mediators of autoimmune diseases. J. Pharmacol. Exp. Ther. 342, 642–653 (2012).
Song, G., Petschauer, J. S., Madden, A. J. & Zamboni, W. C. Nanoparticles and the mononuclear phagocyte system: pharmacokinetics and applications for inflammatory diseases. Curr. Rheumatol. Rev. 10, 22–34 (2014).
Gustafson, H. H., Holt-Casper, D., Grainger, D. W. & Ghandehari, H. Nanoparticle Uptake: The Phagocyte Problem. Nano Today 10, 487–510 (2015).
Getts, D. R., Shea, L. D., Miller, S. D. & King, N. J. Harnessing nanoparticles for immune modulation. Trends Immunol. 36, 419–427 (2015).
Weissleder, R., Nahrendorf, M. & Pittet, M. J. Imaging macrophages with nanoparticles. Nat. Mater. 13, 125–138 (2014).
Rusznyák, I., Földi, M., Szabó, G. & Youlten, L. Lymphatics and Lymph Circulation (Second Edition), (Elsevier, 1967).
Su, D., Shen, M., Li, X. & Sun, L. Roles of gd T cells in the pathogenesis of autoimmune diseases. J. Immunol. Res. 2013, 985756 (2013).
Antonelli, A., Ferrari, S. M., Corrado, A., Di Domenicantonio, A. & Fallahi, P. Autoimmune thyroid disorders. Autoimmun. Rev. 14, 174–180 (2015).
Beeton, C. et al. Selective blocking of voltage-gated K+ channels improves experimental autoimmune encephalomyelitis and inhibits T cell activation. J. Immunol. 166, 936–944 (2001).
Flugel, A., Willem, M., Berkowicz, T. & Wekerle, H. Gene transfer into CD4+ T lymphocytes: green fluorescent protein-engineered, encephalitogenic T cells illuminate brain autoimmune responses. Nat. Med. 5, 843–847 (1999).
Matheu, M. P. et al. Imaging of effector memory T cells during a delayed-type hypersensitivity reaction and suppression by Kv1.3 channel block. Immunity 29, 602–614 (2008).
Kodali, V. et al. Dysregulation of macrophage activation profiles by engineered nanoparticles. ACS Nano 7, 6997–7010 (2013).
Beeton, C. et al. Targeting effector memory T cells with a selective peptide inhibitor of Kv1.3 channels for therapy of autoimmune diseases. Mol. Pharmacol. 67, 1369–1381 (2005).
Beeton, C. & Chandy, K. G. Induction and monitoring of adoptive delayed type hypersensitivity in rats. J. Vis. Exp. 8, e325 (2007).
Brinkmann, V. et al. Fingolimod (FTY720): discovery and development of an oral drug to treat multiple sclerosis. Nat. Rev. Drug Discov. 9, 883–897 (2010).
Rastogi, V. et al. Carbon nanotubes: an emerging drug carrier for targeting cancer cells. J. Drug. Deliv. 2014, 670815 (2014).
Jenkins, M. K. et al. In vivo activation of antigen-specific CD4 T cells. Annu. Rev. Immunol. 19, 23–45 (2001).
Dejaco, C., Duftner, C., Grubeck-Loebenstein, B. & Schirmer, M. Imbalance of regulatory T cells in human autoimmune diseases. Immunology 117, 289–300 (2006).
Fang, F. C. Antimicrobial reactive oxygen and nitrogen species: concepts and controversies. Nat. Rev. Microbiol. 2, 820–832 (2004).
Beeton, C. & Chandy, K. G. Preparing T cell growth factor from rat splenocytes. J. Vis. Exp. 9, e402 (2007).
Beeton, C. & Chandy, K. G. Enrichment of natural killer cells from human blood using the RosetteSep kit from StemCell Technologies. J. Vis. Exp. 8, e326 (2007).
Chang, S. C. et al. Expression and isotopic labeling of the potassium channel blocker ShK toxin as a thioredoxin fusion protein in bacteria. Toxicon 60, 840–850 (2012).
Sano, D. et al. Noncovalent assembly of targeted carbon nanovectors enables synergistic drug and radiation cancer therapy in vivo. ACS Nano 6, 2497–2505 (2012).
Beeton, C. & Chandy, K. G. Drawing blood from the saphenous vein of rats and by cardiac puncture. J. Vis. Exp. 7, e266 (2007).
Lacerda, L. et al. Translocation mechanisms of chemically functionalised carbon nanotubes across plasma membranes. Biomaterials 33, 3334–3343 (2012).
Beeton, C. et al. Kv1.3 channels are a therapeutic target for T cell-mediated autoimmune diseases. Proc. Natl. Acad. Sci. USA 103, 17414–17419 (2006).
Beeton, C. & Chandy, K. G. Induction and monitoring of adoptive delayed-type hypersensitivity in rats. J. Vis. Exp. 8, e325 (2007).
Rashid, M. H. et al. A potent and selective peptide blocker of the Kv1.3 channel: prediction from free-energy simulations and experimental confirmation. Plos ONE 8, e78712 (2013).
Rashid, M. H. et al. A potent and Kv1.3-selective analogue of the scorpion toxin HsTX1 as a potential therapeutic for autoimmune diseases. Sci. Rep. 4, 4509 (2014).
Wulff, H. et al. The voltage-gated Kv1.3 K+ channel in effector memory T cells as new target for MS. J. Clin. Invest. 111, 1703–1713 (2003).
Beeton, C. et al. Selective blockade of T lymphocyte K+ channels ameliorates experimental autoimmune encephalomyelitis, a model for multiple sclerosis. Proc. Natl. Acad. Sci. USA 98, 13942–13947 (2001).
Koshy, S. et al. Blocking Kv1.3 channels inhibits Th2 lymphocyte function and treats a rat model of asthma. J. Biol. Chem. 289, 12623–12632 (2014).
Hu, X. et al. KCa1.1 potassium channels regulate key pro-inflammatory and invasive properties of fibroblast-like synoviocytes in rheumatoid arthritis. J. Biol. Chem. 287, 4014–4022 (2012).
Kopydlowski, K. M. et al. Regulation of macrophage chemokine expression by lipopolysaccharide in vitro and in vivo. J. Immunol. 163, 1537–1544 (1999).
Millien, V. O. et al. Cleavage of fibrinogen by proteinases elicits allergic responses through Toll-like receptor 4. Science 341, 792–796 (2013).
Beeton, C. & Chandy, K. G. Induction and monitoring of active delayed type hypersensitivity (DTH) in rats. J. Vis. Exp. 6, e237 (2007).
Beeton, C., Garcia, A. & Chandy, K. G. Induction and clinical scoring of chronic-relapsing experimental autoimmune encephalomyelitis. J. Vis. Exp. 5, e224 (2007).
Beeton, C. & Chandy, K. G. Isolation of mononuclear cells from the central nervous system of rats with EAE. J. Vis. Exp. 10, e527 (2007).
This work was supported by the Baylor College of Medicine and the National Multiple Sclerosis Society award PP1715 (to C.B.). R.H. was supported by T32 award HL007676 and M.R.T. by T32 awards GM088129 and AI053831 and by F31 award AR069960 from the National Institutes of Health. The Baylor College of Medicine Cytometry & Cell Sorting and Pathology & Histology cores are supported in part by funding from the National Institutes of Health (RR024574, AI036211 and CA125123) and the Dan L. Duncan Cancer Center. The Integrated Microscopy Core at Baylor College of Medicine is supported in part by funding from the National Institutes of Health (HD007495, DK56338 and CA125123), the Dan L. Duncan Cancer Center and the John S. Dunn Gulf Coast Consortium for Chemical Genomics. The work at Rice University was supported by the Traumatic Brain Injury Consortium, funded by the US Army (W81XHW-08-2-0143) and the National Institutes of Health through Baylor College of Medicine (DK093802). We kindly thank Huilong Fei (Department of Chemistry, Rice University) for providing the iron(II,III) oxide nanoparticles, Alexander Flügel (Max-Planck Institute, Martinsried, Germany) for providing the GFP-transduced ovalbumin-specific CD4+ Lewis rat T cells and Evelyne Béraud (Université de la Méditerranée, Marseilles, France) for providing the myelin basic protein-specific CD4+ Lewis rat T cells.
R.H., E.L.G.S., T.I., R.G.P., J.M.T. and C.B. are inventors on a patent application claiming PEG-HCCs as T lymphocyte immunomodulators for the treatment of inflammatory diseases. The patent rights are owned by Rice University and Baylor College of Medicine. These patents have been licensed to Acelerox, LLC in which J.M.T. owns stock. All potential conflicts of interest are managed through the respective institutional offices of research compliance. The other authors declare no competing financial interests.
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Huq, R., Samuel, E., Sikkema, W. et al. Preferential uptake of antioxidant carbon nanoparticles by T lymphocytes for immunomodulation. Sci Rep 6, 33808 (2016). https://doi.org/10.1038/srep33808
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