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Increased expression of OX40 is associated with progressive disease in patients with HTLV-1-associated myelopathy/tropical spastic paraparesis
Retrovirologyvolume 10, Article number: 51 (2013)
OX40 is a member of the tumor necrosis factor receptor family that is expressed primarily on activated CD4+ T cells and promotes the development of effector and memory T cells. Although OX40 has been reported to be a target gene of human T-cell leukemia virus type-1 (HTLV-1) viral transactivator Tax and is overexpressed in vivo in adult T-cell leukemia (ATL) cells, an association between OX40 and HTLV-1-associated inflammatory disorders, such as HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP), has not yet been established. Moreover, because abrogation of OX40 signals ameliorates chronic inflammation in animal models of autoimmune disease, novel monoclonal antibodies against OX40 may offer a potential treatment for HTLV-1-associated diseases such as ATL and HAM/TSP.
In this study, we showed that OX40 was specifically expressed in CD4+ T cells naturally infected with HTLV-1 that have the potential to produce pro-inflammatory cytokines along with Tax expression. We also showed that OX40 was overexpressed in spinal cord infiltrating mononuclear cells in a clinically progressive HAM/TSP patient with a short duration of illness. The levels of the soluble form of OX40 (sOX40) in the cerebrospinal fluid (CSF) from chronic progressive HAM/TSP patients or from patients with other inflammatory neurological diseases (OINDs) were not different. In contrast, sOX40 levels in the CSF of rapidly progressing HAM/TSP patients were higher than those in the CSF from patients with OINDs, and these patients showed higher sOX40 levels in the CSF than in the plasma. When our newly produced monoclonal antibody against OX40 was added to peripheral blood mononuclear cells in culture, HTLV-1-infected T cells were specifically removed by a mechanism that depends on antibody-dependent cellular cytotoxicity.
Our study identified OX40 as a key molecule and biomarker for rapid progression of HAM/TSP. Furthermore, blocking OX40 may have potential in therapeutic intervention for HAM/TSP.
Human T-cell leukemia virus type 1 (HTLV-1) was the first human oncogenic retrovirus to be identified and associated with distinct human diseases such as adult T-cell leukemia (ATL) [1, 2] and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) [3, 4]. HAM/TSP is a chronic progressive myelopathy characterized by spastic paraparesis, sphincter dysfunction, and mild sensory disturbance in the lower extremities . In addition to neurological symptoms, some HAM/TSP patients also exhibit autoimmune-like disorders such as uveitis, arthritis, T-lymphocyte alveolitis, polymyositis, and Sjögren syndrome . Major pathological features of HAM/TSP are chronic inflammation of the spinal cord, characterized by perivascular lymphocytic cuffing and parenchymal lymphocytic infiltration that includes HTLV-1-infected CD4+ T cells . In HAM/TSP patients, the median HTLV-1 proviral load (PVL), which reflects the in vivo number of HTLV-1-infected lymphocytes, is more than 10 times higher than that in asymptomatic carriers (ACs) . An increase in PVL typically coincides with worsening of clinical symptoms . Increased concentrations of inflammatory markers such as neopterin , tumor necrosis factor (TNF)-α, interleukin (IL)-6, and interferon (IFN)-γ , and increase in HTLV-1 antigen-specific intrathecal antibody synthesis  have been observed in the cerebrospinal fluid (CSF) of HAM/TSP patients. More recently, it has been reported that IFN-stimulated genes were overexpressed in circulating leukocytes and the expression correlated with the clinical severity of HAM/TSP . These findings indicate that a pro-inflammatory environment, associated with increased numbers of HTLV-1-infected cells, is a characteristic immunologic profile of HAM/TSP.
OX40, also known as CD134 or TNFRSF4, is a member of the TNF co-stimulatory receptor family and is expressed on activated T cells . OX40 is specifically up-regulated by the HTLV-1 viral transactivator Tax [15, 16]. The ligand of OX40 (OX40L), which belongs to the TNF superfamily, was first identified as glycoprotein 34 (gp34) on HTLV-1-transformed cells , and it was later found to bind OX40 . OX40-OX40L interactions alter the activity and differentiation of many kinds of immune cells, including regulatory T cells (Tregs), T cells, antigen-presenting cells (APCs), natural killer (NK) cells, and natural killer T (NKT) cells . Previous studies have reported that OX40 is constitutively expressed in ATL cells and participate in cell adhesion . Specifically, OX40 and OX40L directly mediate the adhesion of activated normal CD4+ T cells, as well as HTLV-1-transformed T cells, to vascular endothelial cells . Immunohistochemical staining of skin biopsy specimens from ATL patients also showed constitutive expression of OX40, suggesting its role in leukemic cell infiltration, in addition to in vivo cell adhesion .
Recent research has also shown the importance of OX40-OX40L interactions in the development of immune-mediated diseases. In particular, a strong reduction in disease severity or a complete lack of disease has been reported when OX40 or OX40L is absent or neutralized in animal models of multiple sclerosis (MS) , allergic asthma , colitis , diabetes , arthritis , atherosclerosis , graft versus host disease , and allograft rejection . Although HTLV-1 causes an aggressive T cell malignancy (i.e., ATL) and chronic inflammatory diseases such as HAM/TSP, an association of OX40 with the inflammatory diseases observed in HTLV-1-infected individuals has not yet been established.
In this study, we investigated the expression of OX40 in HAM/TSP patients and found that the increased expression of OX40 is associated with the rapidly progressive disease. We also used an in-house monoclonal antibody (mAb) against human OX40 to test the potential of OX40 as a target molecule for immunotherapy.
Tax-dependent constitutive expression of OX40 in HTLV-1-infected T cells
OX40 and OX40L have been reported to be overexpressed in HTLV-1-infected human T-cells lines [15, 19, 20]. These findings were obtained using northern blot or western blot analysis using whole cells; hence, our first aim was to confirm and extend these findings at the single-cell level using flow cytometry. Therefore, we used mAbs against human OX40 (clone B-7B5) and human OX40L (clone 5A8) produced in our laboratory. We analyzed six HTLV-1-infected human T-cell lines (HUT-102, MT-1, MT-2, MT-4, SLB-1, and C5/MJ). C5/MJ, SLB-1, and MT-4 cells have not been previously tested for OX40/OX40L expression. As shown in Figure 1A, expression levels were different in each cell line: OX40 was overexpressed on the surface of the Tax positive (Tax+) T-cell lines (HUT-102, MT-2, MT-4, SLB-1, and C5/MJ), but OX40 was not expressed on the surface of the Tax negative (Tax-) MT-1 cell line or the uninfected T cell line (CEM-OX40L). Consistent with previous studies, these findings suggested that OX40 expression is Tax dependent. In contrast, OX40L was not always expressed on the surface of HTLV-1-infected human T-cell lines or on the uninfected T cell line (CEM-OX40), irrespective of Tax expression (Figure 1B).
Next, we confirmed whether OX40 and OX40L protein expression on the cell surface is induced by Tax at the single-cell level by flow cytometry. We used JPX-9 cells , a Jurkat (HTLV-1 negative human T cell leukemia cell line) subclone generated by stable transfection of a functional Tax expression-plasmid vector, and induced Tax expression by adding CdCl2 into the culture medium (final concentration: 10 μM). As shown in Figure 1C, treatment of JPX-9 cells with CdCl2 induced expression of Tax, and OX40 was expressed exclusively in cells that also expressed Tax. In contrast, OX40L was not expressed in JPX-9 cells even after 96 hours post Tax-induction (Figure 1D).
Previous reports indicated that the soluble forms of OX40 (sOX40) and OX40L (sOX40L) were detectable in serum of patients with autoimmune disease and cancer [30, 31]. We therefore examined whether sOX40 and sOX40L levels were elevated in culture supernatants from HTLV-1 infected T-cell lines and JPX-9 cells before and after induction of Tax. In agreement with our flow cytometry data (Figure 1A), sOX40 was detected in both culture supernatants and cell lysates of Tax positive C5/MJ, HUT102, MT-2, MT-4, and SLB-1 cells (Figure 1E, gray bar). However, sOX40L was not detected in culture supernatants of any of the samples tested, but it was readily detectable in cell lysates of Tax positive C5/MJ, MT-2, MT-4 and SLB1 cells (Figure 1E, light gray bar). We next examined whether soluble OX40 and OX40L are induced by Tax in JPX-9 cells. Addition of CdCl2 to the culture medium of JPX-9 cells resulted in a concomitant increase in sOX40 expression within 24 hours, indicating a strong correlation and functional link between Tax and sOX40 expression (Figure 1F, left panel). Interestingly, although OX40L was already present before induction of Tax, OX40L expression was increased after 24 hours but was never released into the culture supernatant as sOX40L within 120 hours after induction of Tax (Figure 1F, right panel).
Functional OX40 is specifically expressed on the surface of T cells naturally infected with HTLV-1 that have the potential to produce pro-inflammatory cytokines
Next, we tested whether OX40 or OX40L expression is also activated in naturally infected T cells isolated directly from HTLV-1-infected individuals. PBMCs were collected from three non-infected controls (NCs), three ACs, and four HAM/TSP patients. PBMCs were isolated from blood samples and harvested directly, or after a 16-hour in vitro cultivation in the absence of any growth factors or mitogens. After harvesting, cell samples were fixed and processed for concomitant detection of Tax, OX40, or OX40L, and CD4 expression by flow cytometry. Similar to the findings for JPX-9 cells, OX40 was detected with an anti-OX40 mAb (clones B-7B5) after 16 hours of in vitro cultivation (Figure 2A), but OX40L was not detected in cultured PBMCs from a HAM/TSP patient (HAM/TSP1) (Figure 2B). Figure 2C shows that the Tax protein was detected in CD4+ T cells after cultivation. Similar to the JPX-9 cell experiments, OX40 was expressed almost exclusively in the naturally infected CD4+ T cells that also expressed Tax (Figure 2D). Similar findings were observed in all samples tested, irrespective of disease status (i.e., HAM/TSP or ACs) (Additional file 1: Figure S1 and Additional file 2: Table S1). The cells from NCs did not express either OX40 or Tax in CD4+ T cells, before or after cultivation (data not shown). Real time RT-PCR also showed that mRNA expression of HTLV-1 tax and OX40 in CD4+ T cells was increased after cultivation, both in HAM/TSP patients and ACs (Figure 2E).
It has recently been reported , that the expression of another co-stimulatory member of the TNFR family, 4-1BB, is also up-regulated ex vivo in CD4+ T cells from HTLV-1-infected individuals, and it was found to be correlated with Tax expression (Additional file 1: Figure S2A and B). However, the expression of OX40 is more specific for Tax+CD4+ cells than 4-1BB (Figure 2D and Additional file 1: Figure S2C).
Next, we sought to determine if OX40, expressed on the surface of Tax+CD4+ T cells from HTLV-1-infected individuals, is functional. We incubated aliquots of Fc-blocked PBMCs with biotinylated recombinant soluble OX40L at a concentration of 2.5 mg/ml for 30 min on ice. Cells were then fixed and processed for concomitant detection of Tax, CD4, and PE-streptavidin by flow cytometry. As shown in Additional file 1: Figure S3, the frequency of CD4+ T cells that were positively stained with biotinylated recombinant soluble OX40L and PE-streptavidin was similar to the percentage of CD4+ T cells stained by anti-OX40 mAb, indicating that these cells expressed functional OX40.
We further analyzed if CD4+OX40+ T cells in HAM/TSP patients were capable of producing the inflammatory and neurotoxic cytokines, IFN-γ and TNF-α, which, according to the bystander damage hypothesis, could cause central nervous system (CNS) inflammation and demyelination seen in HAM/TSP patients [33, 34]. The frequency of pro-inflammatory cytokine positive cells within the OX40+CD4+ and Tax+CD4+ populations from HAM/TSP patients are significantly higher than OX40-CD4+ and Tax-CD4+ T cells, respectively (p < 0.001, Student's t- test) (Figure 2F and Table 1).
Increased expression of OX40 in vivo in rapidly progressive HAM/TSP patients
To investigate if OX40 expression is associated with in vivo pathogenesis of HAM/TSP, we first measured the plasma concentration of sOX40 and sOX40L in 20 chronic HAM/TSP patients, 9 ACs, and 13 NCs by ELISA by using monoclonal antibodies generated in our laboratory (Figure 3A). None of the samples had detectable levels of sOX40L (data not shown), but we could readily detect sOX40. The median level of sOX40 in NCs was 149.5 pg/ml (range 13–328 pg/ml). Significantly higher sOX40 levels were found in chronic HAM/TSP patients (median 395.2 pg/ml, range 113–1295 pg/ml) and ACs (median 423.8 pg/ml, range 201–881 pg/ml) than in NCs (p=0.0043 for differences between HAM/TSP and NCs, p=0.0020 for differences between ACs and NCs). The difference between chronic HAM/TSP patients and ACs was not statistically significant. No positive correlation was found between sOX40 in the plasma and HTLV-1 PVL in infected individuals (i.e., chronic HAM/TSP patients and ACs) (Spearman’s rank correlation coefficient n=29, r=0.031, P=0.873; Figure 3B). We then tested disease specificity by measuring the levels of sOX40 in the CSF from both rapidly progressive and chronic HAM/TSP patients, and in patients with other neurological disorders, with and without inflammation (e.g., 12 MS, 8 aseptic meningitis, 5 systemic lupus erythematosus with neurological manifestations, 9 chronic inflammatory demyelinating polyneuropathy, 6 Guillain-Barré syndrome, and 9 amyotrophic lateral sclerosis patients). As shown in Figure 3C, CSF sOX40 levels were markedly increased in patients with rapidly progressive HAM/TSP (n=3) and aseptic meningitis (n=8). The CSF sOX40 levels in other HTLV-1-infected inflammatory neurological diseases, i.e. any inflammatory neurological disorders except for HAM/TSP that occurred in HTLV-1 infected individuals, (HTLV-1+ OINDs, n=6) was not significantly different from chronic HAM/TSP (n=20), whereas the sOX40 level of HTLV-1+ OINDs was significantly increased compared to non-infected OINDs (HTLV-1- OINDs, n=26; Figure 3D).
Of the HAM/TSP patients studied, paired CSF and plasma samples, i.e., blood and CSF were collected on the same day, were available for six patients. HAM/TSP patients No.10-12 had a lower concentration of sOX40 in the CSF than in the plasma (Table 2), and the patients showed a typical clinical course of HAM/TSP (i.e. slowly progressive symmetrical myelopathy) and had no history of rapid exacerbation. In contrast, HAM/TSP patients No.13-15, who had higher concentrations of sOX40 in the CSF than in the plasma, showed a rapidly progressive clinical course (i.e. patients became unable to walk within three months after onset of initial symptoms).
Expression of OX40 in inflammatory mononuclear cells in spinal cord lesions of HAM/TSP patient with short disease duration and progressive symptoms
We also examined autopsy specimens from HAM/TSP patients by immunohistochemical staining. Although there was reduced or no OX40 protein expression in HAM/TSP patients who had a long duration of illness and who no longer had active inflammation (a representative example is shown in Figure 4A), we observed marked OX40 expression in inflammatory round-shaped mononuclear cells around the blood vessels in spinal cord lesions from one HAM/TSP patient (Figure 4B). This patient (patient 1 in refs [35–38], who had a shorter disease duration of up to 2.5 years after the onset of neurological symptoms) showed predominant infiltration of CD4+ T cells  that also expressed tax mRNA , pro-inflammatory cytokines , and matrix metalloproteinases . In contrast, we observed only low background staining for OX40L in spinal cord tissues of all the HAM/TSP patients examined (a representative example is shown in Figure 4C) compared to positive control (Figure 4D).
Anti-OX40 monoclonal antibody specifically eliminated naturally infected CD4+T cells via antibody-dependent cell-mediated cytotoxicity (ADCC) in cultured PBMCs
We investigated the role of OX40 in HTLV-1 naturally infected CD4+ T cells, by testing the effects of an anti-human OX40 mAb on Tax expression. As shown in Figure 5, anti-OX40 mAb (clone B-7B5) reduced the percentage of Tax-positive cells, whereas the isotype control mAb (clone 2C2: anti-HIV-1 gp21, mouse IgG1) had no effect on Tax expression (Figure 5, 1st, 2nd, and 3rd panels from left). Culture of PBMCs with anti-CD16/CD32 (Fc receptor) antibody to block Fc receptors abolished Tax suppression by anti-OX40 mAb (Figure 5, 4th panels from left), suggesting that the effect of the anti-OX40 mAb (B-7B5) is mainly mediated by ADCC. We further tested the effects of the F(ab’)2 fragment of anti-OX40 mAb (B-7B5) and found that the F(ab’)2 fragment did not suppress Tax expression; this finding supports an ADCC mechanism of action of the anti-OX40 mAb (Figure 5, right panels).
Anti-OX40 monoclonal antibody specifically eliminated OX40-positive HTLV-1 infected cells in cultured PBMCs
We examined whether suppression of OX40 expression either reduced the frequency of Tax-positive cells or selectively eliminated HTLV-1-infected cells by isolating CD4+ T cells from PBMCs before and after culture, extracting genomic DNA, and measuring HTLV-1 PVL. HTLV-1 PVL in CD4+ T cells was significantly reduced after culture, suggesting that the anti-OX40 mAb (B-7B5) did not suppress expression of Tax but specifically eliminated OX40-positive HTLV-1 infected cells (Figure 6).
Retroviral infection is characterized by chronic immune-system activation and pro-inflammatory cytokine production . HTLV-1 infection is associated with the development of several different inflammatory conditions, including chronic arthritis, pulmonary alveolitis, polymyositis, Sjögren syndrome, and uveitis . The main pathological feature of HAM/TSP is chronic inflammation of the spinal cord, characterized by perivascular cuffing of mononuclear cells accompanied by parenchymal lymphocytic infiltration. Increased spontaneous peripheral blood lymphocyte proliferation with the production of TNF-α and IFN-γ [42, 43], high prevalence of autoantibodies, hypergammaglobulinemia, and complement fixing immune complexes have also been reported in HAM/TSP patients . Recent research has shown the importance of OX40-OX40L interactions in the development of immune-mediated diseases. Specifically, a strong reduction in disease severity, or a complete lack of disease, has been reported when OX40 or OX40L is absent or neutralized in animal models. We therefore hypothesized that the OX40-positive subpopulations of chronically activated T cells exist in naturally HTLV-1-infected cells of HAM/TSP patients. These cells may function to accelerate inflammation, and blocking OX40 may have therapeutic potential in the treatment of HAM/TSP.
Previous reports indicated that OX40 is strongly stimulated by the HTLV-1 viral transactivator Tax [15, 19, 20]. However, these previous findings were obtained by northern blot or western blot analysis using whole cells. Thus, it was not clear if this induction occurs in naturally infected CD4+ T cells of HTLV-1 infected individuals. In the present study, our flow cytometry analysis clearly showed that almost all OX40-positive cells are Tax-positive after short-term culture of naturally HTLV-1-infected cells, suggesting that OX40 is driven exclusively by Tax at the single cell level. In contrast, flow cytometry analysis of JPX-9 cells showed higher percentages of OX40+Tax- cells, as well as OX40+Tax+ cells, after induction of Tax. Although the reasons for this discrepancy are not clear, it can be caused by differential modulation of surface and intracellular protein expression in JPX-9 cells. Our ELISA analysis indicates the existence of intracellular pools of OX40, suggesting that Tax+OX40- cells also contain Tax-induced OX40 within JPX-9 cells. While the expression of another co-stimulatory member of the TNFR family, 4-1BB, has also been reported , our data indicate that the expression of OX40 was more specific than the expression of 4-1BB in Tax+CD4+ T cells naturally infected with HTLV-1. It has been previously reported that Tax strongly activates the 4-1BB promoter via a single NF-κB site  and the OX40 promoter via 2 NF-κB sites ; hence, sustained activation of NF-κB leads to increased expression of numerous pro-inflammatory cytokines and growth factors  via NF-κB signaling pathways and ultimately leads to chronic inflammation. In support of these observations, our results show that the frequencies of pro-inflammatory cytokine positive cells within the OX40+CD4+ and Tax+CD4+ populations from HAM/TSP patients are significantly higher than OX40-CD4+ and Tax-CD4+ T cells, respectively. These cells may be more likely to cross the blood brain barrier and enter the CNS, attract other cells including pro-inflammatory virus-specific CD8+ cells, and result in bystander damage to the CNS tissue.
The experimental autoimmune encephalomyelitis (EAE) rat model of human MS shows a selective upregulation of the OX40 protein in encephalitogenic myelin basic protein-specific T cells in the spinal cord during onset of the disease . In contrast, T cells isolated from peripheral blood and spleen of the same animal express low levels of OX40 . This is similar to our present finding, where OX40 was markedly expressed in infiltrating mononuclear cells in spinal cord lesions, but not in uncultivated PBMCs from HAM/TSP patients. Because locally produced pro-inflammatory cytokines up-regulate MHC class II molecules on astrocytes and microglia, increase presentation of CNS antigens, and exert a direct cytotoxic effect on oligodendrocytes , the observed expression of OX40 in inflammatory mononuclear cells in spinal cord lesions suggest a role for OX40 in inflammation and neuronal damage that occurs in the CNS of HAM/TSP patients. In the rat EAE model, selective depletion of myelin-reactive T cells, by treatment with an anti-OX40 mAb-conjugated immunotoxin, effectively suppressed disease symptoms . The association of clinical progression of HAM/TSP with increased HTLV-1 PVL in individual patients  and the strong stimulation of OX40, together with the expression of the viral transactivator Tax in CD4+ T cells, indicates that targeting of OX40 positive T cells by anti-OX40 antibodies may provide a novel therapeutic strategy for the treatment of HAM/TSP.
In the present study, an anti-OX40 monoclonal antibody specifically eliminated naturally infected CD4+ T cells in cultured PBMCs via ADCC. This indicates that effector cells may actively lyse HTLV-1-infected CD4+ T cells that are bound by the anti-OX40 antibody. Indeed, defucosylated humanized anti-CC chemokine receptor 4 (CCR4) mAbs, which exert a strong ADCC effect, were found to be effective and well tolerated as a treatment for patients with relapsed CCR4-positive ATL or peripheral T-cell lymphoma . In the present study, OX40 expression was not observed in T cells of healthy individuals, and its expression was more specific than CCR4 for HTLV-1-infected cells. This finding suggests that specific elimination of HTLV-1-infected T cells by defucosylated humanized anti-OX40 monoclonal antibodies might be a promising future approach for treatment of HAM/TSP.
We also found that plasma sOX40 levels were more elevated in HTLV-1-infected individuals (chronic HAM/TSP patients and ACs) than in NCs. Three rapidly progressive HAM/TSP patients also showed higher levels of sOX40 in the CSF than in the plasma, suggesting the possibility that sOX40 is released at high levels following strong intrathecal immune activation. In contrast, expression of OX40L was absent in HTLV-1-infected lymphocytes even after short term ex vivo cultivation, in active-chronic spinal cord lesions of HAM/TSP patient, and in plasma of HTLV-1 infected individuals. Therefore, OX40 signals might be generated by interactions with OX40L on antigen presenting cells or endothelial cells at specialized sites such as lymphoid organs. In such lesions, similar to other members of the TNF receptor superfamily like 4-1BB, sOX40 may act as an antagonist to membrane-bound receptors and induce signaling in OX40L+ cells to produce cytokines, which in turn drive specific T helper (Th)-cell differentiation and suppress the generation of adaptive Tregs to participate in HAM/TSP pathogenesis.
In conclusion, we demonstrate that OX40 was specifically expressed in CD4+ T cells naturally infected with HTLV-1. These cells have the potential to produce pro-inflammatory cytokines along with the expression of the viral transactivator Tax. Higher levels of sOX40 were found in the CSF than in the plasma of three rapidly progressive HAM/TSP patients, and OX40 was overexpressed in the spinal cord infiltrating mononuclear cells of HAM/TSP patient with active disease. Anti-OX40 mAb was able to specifically eliminate HTLV-1-infected CD4+OX40+Tax+ T cells via ADCC. These findings indicate that, in addition to its established role in the regulation of T cell division and survival, OX40 may be a key molecule in the pathogenesis of HAM/TSP, as well as a potential target for immunotherapy.
Peripheral blood was studied from 23 patients with a clinical diagnosis of HAM/TSP, 9 ACs and 13 uninfected normal controls (NCs). The diagnosis of HAM/TSP was made according to the World Health Organization diagnostic criteria . In this paper, chronic HAM/TSP means typical cases fulfilling diagnostic criteria and rapidly progressive HAM/TSP is defined by patients’ incapacity to walk unaided within three months after symptoms’ onset. This study was approved by the Institutional Review Board of the University of the Ryukyus with license number H21-1-9. All patients provided written informed consent for the collection of samples and subsequent analysis. The CSF and plasma samples were collected before starting therapy. Control subjects of other neurological diseases were MS (n=12), aseptic meningitis (n=8), systemic lupus erythematosus (SLE) with neurological manifestations (n=5), chronic inflammatory demyelinating polyneuropathy (CIDP) (n=9), Guillain-Barré syndrome (GBS) (n=6), and amyotrophic lateral sclerosis (ALS) (n=9). The specimens were stored at −80°C until use.
Six HTLV-1 infected T-cell lines (HUT-102, MT-1, MT-2, MT-4, SLB-1, C5/MJ) and two HTLV-1-uninfected T-cell lines (CEM-OX40L, CEM-OX40) were used in this study. CEM-OX40 and CEM-OX40L cell lines are stable CEM-derived cell lines expressing the human OX40 or OX40L, respectively. The Tax-inducible JPX-9 cell line is a derivative of the Jurkat HTLV-1 negative human T cell leukemia cell line, which expresses biologically active Tax protein under the control of the metallothionein promoter . These cells were cultured in RPMI 1640 medium supplemented with 10% heat inactivated fetal calf serum (FCS), 50 U/ml penicillin, and 50 μg/ml streptomycin (Wako) at 37°C in 5% CO2.
Preparation of PBMC samples
Fresh peripheral blood mononuclear cells (PBMCs) were isolated on a Histopaque-1077 (Sigma) density gradient centrifugation, washed twice in RPMI 1640 with 10% heat inactivated FCS, and stored in liquid nitrogen as stocked lymphocytes until use. CD4+ T cells were isolated from PBMCs by positive immunoselection with the Dynal® CD4-positive isolation kit (Invitrogen), according to the manufacturer’s protocol. In brief, PBMCs were incubated with anti-CD4-coated beads for 30 min at 4°C under gentle tilt rotation. Captured CD4+ cells were collected with a magnet (Dynal MPC-S) and detached from beads with DETACHaBEAD CD4/CD8® (Invitrogen). Purity was >99% CD4+ T cells, as determined by flow cytometry (data not shown). To induce cytokine production by OX40+CD4+ T cells, PBMCs were cultivated for 12 hours, then 0.1 ng/ml phorbol myristate acetate (PMA) (Sigma) and 0.5 μg/ml A23187 (Sigma) and 2 mM monensin (Sigma) were added to the culture medium and further cultivated for 5 hours.
Monoclonal antibodies and reagents
We produced the following monoclonal antibodies (mAbs) in our laboratory: mouse IgG1 mAbs anti-human OX40L (clones 5A8, 8F4), anti-human OX40 (clones B-7B5 and 17D8), anti-HIV-1 p24 (clone 2C2 and NP24), and mouse IgG3 mAb anti-HTLV-1 Tax (clone Lt-4)  as well as rat IgG2b mAbs anti-human OX40 (clone W4-54), anti-human OX40L (clone W18) and isotype control anti-HCV (clone MO-8). Some of these mAbs were labeled using FITC, Cy5, or HRP using commercial labeling kits (Dojin or Amersham, Japan) according to the manufacturers’ instructions. Biotinylated recombinant soluble human OX40L (sOX40L in a form of murine CD8-fusion protein) was purchased from Ancell (Bayport, MN) and used with PE-streptavidin (Biolegend) for staining. Recombinant human OX40 ligand/TNFSF4 and recombinant human OX40/TNFRSF4/Fc Chimera were purchased from R&D Systems (Minneapolis, MN) and used for the standard curve in sOX40L and sOX40 ELISA, respectively.
Immunohistochemical staining of the spinal cord specimens from HAM/TSP patients was performed on buffered formalin-fixed paraffin-embedded sections using EnVision (DAKO) method for signal detection as described previously . The clinical and pathological characteristics of the patients are described elsewhere [36–39]. The monoclonal antibodies to OX40 (clone B-7B5) and OX40L (clone 8F4) were used at a final concentration of 1 μg/ml.
Cell surface staining
After thawing, cells were washed three times with phosphate-buffered saline (PBS) and fixed in PBS containing 2% paraformaldehyde (Sigma) for 20 minutes at 4°C. Fixed cells were washed with PBS containing 7% of normal goat serum (Sigma) and then incubated for 15 minutes at room temperature with various combinations of fluorescence-conjugated mAbs as follows: phycoerythrin-cyanin 5.1 (PC5)-labeled anti-CD4 (13B8.2), PC5-labeled anti-CD8 (B9.11), phycoerythrin (PE)-labeled anti-CD4 (13B8.2) (Beckman Coulter), PE-labeled anti-4-1BB (4B4) (eBioscience), fluorescein isothiocyanate (FITC)-labeled anti-OX40 (B-7B5) and OX40L (5A8). Isotype matched mouse immunoglobulins were used as a control. After the staining procedure, the cells were washed twice and analyzed by standard flow cytometry using a FACS Calibur and Cell Quest software (BD).
Concomitant detection of intracellular and cell surface molecules
For intracellular staining of Tax and/or cytokines, surface stained cells were washed and permeabilized with PBS/7% normal goat serum containing 0.2% saponin (Sigma) (PBS-SAPO) for 10 minutes at room temperature. Permeabilized cells were then washed twice and resuspended in PBS-SAPO containing FITC or cyanin 5 (Cy5)-labeled anti-Tax mAb (Lt-4), PE-labeled anti TNF-α (BD Pharmingen) or PE-labeled IFN-γ (BD Pharmingen) mAb for 20 minutes at room temperature. Finally, the cells were washed twice and analyzed by flow cytometry.
Flow cytometry based binding assay
To determine whether cell surface OX40 is functional, aliquots of Fc-blocked cells were incubated with biotinylated recombinant soluble OX40L at a concentration of 2.5 mg/ml for 30 min on ice, followed by staining with PE-streptavidin (Biolegend) for 30 min on ice. After the staining procedure, the cells were washed twice and analyzed by flow cytometry.
Cell lysates were prepared by lysis of 2 × 107 cells in 1ml of a lysis buffer (10 mM Tris–HCl, pH8.0, 140 mM NaCl, 3 mM MgCls, 2 mM phenylmethylsulfonyl fluoride, 0.5% Nonidet P-40) on ice for 20 min, followed by centrifugation at 13,000 × g for 10 min at 4°C. Both OX40 and OX40L levels in cell lysates, culture supernatants, plasma and CSF were assayed by in house made sandwich ELISA using monoclonal antibodies against OX40 (clone 17D8 for capture and W4-54 for detection) and OX40L (clone 8F4 for capture and W18 for detection). Briefly, 96-well Immuno Module/Strip Plates (Nunc) was coated with either anti-OX40 monoclobal antibody (clone 17D8) or anti-OX40L monoclobal antibody (clone 8F4) at 4°C overnight, then blocked with 1% casein in 0.02% thimerosal-PBS at room temperature for 30 min. After washing plates three times with wash buffer (PBS with 0.05% Tween 20, pH 7.5), 50 μl of irrelevant mouse IgG1 (anti-HIV1 p24 mAb NP24) was added into each well as a blocking antibody. OX40 or OX40L standard was diluted to 4,000 pg/ml in dilution buffer (PBS with 0.1% BSA, 0.5% Triton X100, 0.05% Tween20), and two-fold serial dilutions were performed ranged from 4,000 to 16 pg/ml. Then 50 μl of the diluted standard or samples (cell lysates, culture supernatants, plasma and CSF) were added into 96-well plates and incubated one hour at room temparature. After washing plates three times, 50 μl each of diluted (0.2 μg/μl) anti-OX40 monoclobal antibody (clone W4-54) or anti-OX40L monoclobal antibody (clone W18) conjugated to HRP was added as detection antibody and incubated for one hour at room temperature. Color reactions using alkaline-phosphatase substrate (Sigma-Aldrich) were then evaluated by Model 680 Microplate Reader (Bio-Rad) reading at 450 nm with reference at 630 nm, and the data was analyzed using the Microplate manager III software (Bio-Rad). Results are shown as mean ± SE for duplicate wells. Human interleukin-2 soluble receptor alpha (IL-2sRα) was measured by ELISA according to the manufacturer’s instruction (Quantikine Human IL-2sRα Immunoassay, R&D Systems, Inc. MN).
Genomic DNA, RNA extraction and cDNA synthesis
Genomic DNA was extracted from the frozen PBMCs by QIAamp blood kit (QIAGEN, Tokyo, Japan). RNA from 1×105 enriched CD4+ T cells was extracted using RNeasy Mini Kit with on-column DNase digestion (QIAGEN, Tokyo, Japan) according to the manufacturer’s instructions. Complementary DNA (cDNA) was synthesized using PrimeScript® RT reagent Kit (Takara, Kyoto, Japan). All reaction procedures were performed as suggested by the manufacturer.
Quantification of HTLV-1 proviral load and anti-HTLV-1 antibody titers
To examine the HTLV-1 PVL, we carried out a quantitative PCR method using Thermal Cycler Dice® Real Time System (Takara, Japan) with 100 ng of genomic DNA (roughly equivalent to 104 cells) from PBMCs samples as reported previously . Based on the standard curve created by four known concentrations of template, the concentration of unknown samples were determined. Using β-actin as an internal control, the amount of HTLV-1 proviral DNA was calculated by the following formula: copy number of HTLV-1 tax per 1 × 104PBMCs = [(copy number of tax)/(copy number of β − actin/2)] × 104. All samples were performed in triplicate. Serum HTLV-1 antibody titers were determined by a particle agglutination method (Serodia-HTLV-1®, Fujirebio, Japan).
Real-Time RT-PCR analysis
We used the real-time RT-PCR method to carry out a quantitative analysis of the expression of the tax and OX40 mRNA by using Thermal Cycler Dice® Real Time System (Takara, Japan) as reported previously . HTLV-1 tax or OX40 mRNA load was calculated by the following formula: HTLV - 1 tax mRNA load = value of tax/value of HPRT (Hypoxanthine Phosphorisbosytransferase). OX40 mRNA load = value of OX40/value of HPRT. We used aliquots of the same standard MT-2 cDNA preparation for all assays and the correlation values of standard curves were always more than 99%. The sequences of primers for tax mRNA detection were as follows: 5′- ATC CCG TGG AGA CTC CTC AA-3′ and 5′- ATC CCG TGG AGA CTC CTC AA-3′, and the probe that surrounded the splice junction site of tax mRNA was 5′- TCC AAC ACC ATG GCC CAC TTC CC-3′. The sequences of primers for OX40 mRNA detection were as follows: 5′-AAC CAG GCC TGC AAG CCC T-3′ and 5′- GTC CCT GTC CTC ACA GAT T-3′, and the probe that span the junction between exon 4 and 5 was 5′- ACC AAC TGC ACC TTG GCT GGG AAG CA-3′. We used the HPRT primers and probe set (Applied Biosystems) for internal calibration. All assays were performed in triplicate.
To test for significant differences among the cell populations between three different groups of subjects (HAM/TSP, ACs and NCs), the Kruskal-Wallis test was employed. For multiple comparisons, we used Sheffe’s F to analyze statistical difference. Correlations between variables were examined by Spearman rank correlation analysis. We made paired comparison of changes in HTLV-1 PVL in CD4+ T cells before and after PBMCs cultivation by using a paired t-test. The results represent the mean ± SE where applicable. Values of p<0.05 were considered statistically significant.
Human T-cell leukemia virus type-1
Adult T-cell leukemia
HTLV-1-associated myelopathy/tropical spastic paraparesis
Normal uninfected healthy controls
Other inflammatory neurological diseases
Antibody-dependent cellular cytotoxicity
Central nervous system
Systemic lupus erythematosus
Chronic inflammatory demyelinating polyneuropathy
Amyotrophic lateral sclerosis
Yoshida M, Seiki M, Yamaguchi K, Takatsuki K: Monoclonal integration of human T-cell leukemia provirus in all primary tumors of adult T-cell leukemia suggests causative role of human T-cell leukemia virus in the disease. Proc Natl Acad Sci USA. 1984, 81: 2534-2537. 10.1073/pnas.81.8.2534.
Hinuma Y, Nagata K, Hanaoka M, Nakai M, Matsumoto T, Kinoshita KI, Shirakawa S, Miyoshi I: Adult T-cell leukemia: antigen in an ATL cell line and detection of antibodies to the antigen in human sera. Proc Natl Acad Sci USA. 1981, 78: 6476-6480. 10.1073/pnas.78.10.6476.
Osame M, Usuku K, Izumo S, Ijichi N, Amitani H, Igata A, Matsumoto M, Tara M: HTLV-I associated myelopathy, a new clinical entity. Lancet. 1986, 1: 1031-1032.
Gessain A, Barin F, Vernant JC, Gout O, Maurs L, Calender A, de The G: Antibodies to human T-lymphotropic virus type-I in patients with tropical spastic paraparesis. Lancet. 1985, 2: 407-410.
Nakagawa M, Nakahara K, Maruyama Y, Kawabata M, Higuchi I, Kubota H, Izumo S, Arimura K, Osame M: Therapeutic trials in 200 patients with HTLV-I-associated myelopathy/ tropical spastic paraparesis. J Neurovirol. 1996, 2: 345-355. 10.3109/13550289609146899.
Nakagawa M, Izumo S, Ijichi S, Kubota H, Arimura K, Kawabata M, Osame M: HTLV-I-associated myelopathy: analysis of 213 patients based on clinical features and laboratory findings. J Neurovirol. 1995, 1: 50-61. 10.3109/13550289509111010.
Izumo S, Umehara F, Osame M: HTLV-I-associated myelopathy. Neuropathology. 2000, 20 (Suppl): S65-68.
Nagai M, Usuku K, Matsumoto W, Kodama D, Takenouchi N, Moritoyo T, Hashiguchi S, Ichinose M, Bangham CR, Izumo S, Osame M: Analysis of HTLV-I proviral load in 202 HAM/TSP patients and 243 asymptomatic HTLV-I carriers: high proviral load strongly predisposes to HAM/TSP. J Neurovirol. 1998, 4: 586-593. 10.3109/13550289809114225.
Takenouchi N, Yamano Y, Usuku K, Osame M, Izumo S: Usefulness of proviral load measurement for monitoring of disease activity in individual patients with human T-lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis. J Neurovirol. 2003, 9: 29-35.
Nomoto M, Utatsu Y, Soejima Y, Osame M: Neopterin in cerebrospinal fluid: a useful marker for diagnosis of HTLV-I-associated myelopathy/tropical spastic paraparesis. Neurology. 1991, 41: 457-
Jacobson S: Immunopathogenesis of human T cell lymphotropic virus type I-associated neurologic disease. J Infect Dis. 2002, 186 (Suppl 2): S187-192.
Kitze B, Usuku K, Yashiki S, Ijichi S, Fujiyoshi T, Nakamura M, Izumo S, Osame M, Sonoda S: Intrathecal humoral immune response in HAM/TSP in relation to HLA haplotype analysis. Acta Neurol Scand. 1996, 94: 287-293. 10.1111/j.1600-0404.1996.tb07067.x.
Tattermusch S, Skinner JA, Chaussabel D, Banchereau J, Berry MP, McNab FW, O’Garra A, Taylor GP, Bangham CR: Systems biology approaches reveal a specific interferon-inducible signature in HTLV-1 associated myelopathy. PLoS Pathog. 2012, 8: e1002480-10.1371/journal.ppat.1002480.
Croft M: Control of immunity by the TNFR-related molecule OX40 (CD134). Annu Rev Immunol. 2010, 28: 57-78. 10.1146/annurev-immunol-030409-101243.
Higashimura N, Takasawa N, Tanaka Y, Nakamura M, Sugamura K: Induction of OX40, a receptor of gp34, on T cells by trans-acting transcriptional activator, Tax, of human T-cell leukemia virus type I. Jpn J Cancer Res. 1996, 87: 227-231. 10.1111/j.1349-7006.1996.tb00210.x.
Pankow R, Durkop H, Latza U, Krause H, Kunzendorf U, Pohl T, Bulfone-Paus S: The HTLV-I tax protein transcriptionally modulates OX40 antigen expression. J Immunol. 2000, 165: 263-270.
Tanaka Y, Inoi T, Tozawa H, Yamamoto N, Hinuma Y: A glycoprotein antigen detected with new monoclonal antibodies on the surface of human lymphocytes infected with human T-cell leukemia virus type-I (HTLV-I). Int J Cancer. 1985, 36: 549-555. 10.1002/ijc.2910360506.
Baum PR, Gayle RB, Ramsdell F, Srinivasan S, Sorensen RA, Watson ML, Seldin MF, Baker E, Sutherland GR, Clifford KN: Molecular characterization of murine and human OX40/OX40 ligand systems: identification of a human OX40 ligand as the HTLV-1-regulated protein gp34. EMBO J. 1994, 13: 3992-4001.
Imura A, Hori T, Imada K, Kawamata S, Tanaka Y, Imamura S, Uchiyama T: OX40 expressed on fresh leukemic cells from adult T-cell leukemia patients mediates cell adhesion to vascular endothelial cells: implication for the possible involvement of OX40 in leukemic cell infiltration. Blood. 1997, 89: 2951-2958.
Imura A, Hori T, Imada K, Ishikawa T, Tanaka Y, Maeda M, Imamura S, Uchiyama T: The human OX40/gp34 system directly mediates adhesion of activated T cells to vascular endothelial cells. J Exp Med. 1996, 183: 2185-2195. 10.1084/jem.183.5.2185.
Weinberg AD, Bourdette DN, Sullivan TJ, Lemon M, Wallin JJ, Maziarz R, Davey M, Palida F, Godfrey W, Engleman E: Selective depletion of myelin-reactive T cells with the anti-OX-40 antibody ameliorates autoimmune encephalomyelitis. Nat Med. 1996, 2: 183-189. 10.1038/nm0296-183.
Salek-Ardakani S, Song J, Halteman BS, Jember AG, Akiba H, Yagita H, Croft M: OX40 (CD134) controls memory T helper 2 cells that drive lung inflammation. J Exp Med. 2003, 198: 315-324. 10.1084/jem.20021937.
Higgins LM, McDonald SA, Whittle N, Crockett N, Shields JG, MacDonald TT: Regulation of T cell activation in vitro and in vivo by targeting the OX40-OX40 ligand interaction: amelioration of ongoing inflammatory bowel disease with an OX40-IgG fusion protein, but not with an OX40 ligand-IgG fusion protein. J Immunol. 1999, 162: 486-493.
Pakala SV, Bansal-Pakala P, Halteman BS, Croft M: Prevention of diabetes in NOD mice at a late stage by targeting OX40/OX40 ligand interactions. Eur J Immunol. 2004, 34: 3039-3046. 10.1002/eji.200425141.
Yoshioka T, Nakajima A, Akiba H, Ishiwata T, Asano G, Yoshino S, Yagita H, Okumura K: Contribution of OX40/OX40 ligand interaction to the pathogenesis of rheumatoid arthritis. Eur J Immunol. 2000, 30: 2815-2823. 10.1002/1521-4141(200010)30:10<2815::AID-IMMU2815>3.0.CO;2-#.
van Wanrooij EJ, van Puijvelde GH, de Vos P, Yagita H, van Berkel TJ, Kuiper J: Interruption of the Tnfrsf4/Tnfsf4 (OX40/OX40L) pathway attenuates atherogenesis in low-density lipoprotein receptor-deficient mice. Arterioscler Thromb Vasc Biol. 2007, 27: 204-210. 10.1161/01.ATV.0000251007.07648.81.
Tsukada N, Akiba H, Kobata T, Aizawa Y, Yagita H, Okumura K: Blockade of CD134 (OX40)-CD134L interaction ameliorates lethal acute graft-versus-host disease in a murine model of allogeneic bone marrow transplantation. Blood. 2000, 95: 2434-2439.
Curry AJ, Chikwe J, Smith XG, Cai M, Schwarz H, Bradley JA, Bolton EM: OX40 (CD134) blockade inhibits the co-stimulatory cascade and promotes heart allograft survival. Transplantation. 2004, 78: 807-814. 10.1097/01.TP.0000131670.99000.54.
Nagata K, Ohtani K, Nakamura M, Sugamura K: Activation of endogenous c-fos proto-oncogene expression by human T-cell leukemia virus type I-encoded p40tax protein in the human T-cell line, Jurkat. J Virol. 1989, 63: 3220-3226.
Taylor L, Schwarz H: Identification of a soluble OX40 isoform: development of a specific and quantitative immunoassay. J Immunol Methods. 2001, 255: 67-72. 10.1016/S0022-1759(01)00424-0.
Komura K, Yoshizaki A, Kodera M, Iwata Y, Ogawa F, Shimizu K, Wayaku T, Yukami T, Murata M, Hasegawa M: Increased serum soluble OX40 in patients with systemic sclerosis. J Rheumatol. 2008, 35: 2359-2362. 10.3899/jrheum.080120.
Pichler K, Kattan T, Gentzsch J, Kress AK, Taylor GP, Bangham CR, Grassmann R: Strong induction of 4-1BB, a growth and survival promoting costimulatory receptor, in HTLV-1-infected cultured and patients’ T cells by the viral Tax oncoprotein. Blood. 2008, 111: 4741-4751. 10.1182/blood-2007-10-115220.
Ijichi S, Izumo S, Eiraku N, Machigashira K, Kubota R, Nagai M, Ikegami N, Kashio N, Umehara F, Maruyama I: An autoaggressive process against bystander tissues in HTLV-I-infected individuals: a possible pathomechanism of HAM/TSP. Med Hypotheses. 1993, 41: 542-547. 10.1016/0306-9877(93)90111-3.
Daenke S, Bangham CR: Do T cells cause HTLV-1-associated disease?: a taxing problem. Clin Exp Immunol. 1994, 96: 179-181.
Umehara F, Nakamura A, Izumo S, Kubota R, Ijichi S, Kashio N, Hashimoto K, Usuku K, Sato E, Osame M: Apoptosis of T lymphocytes in the spinal cord lesions in HTLV-I-associated myelopathy: a possible mechanism to control viral infection in the central nervous system. J Neuropathol Exp Neurol. 1994, 53: 617-624. 10.1097/00005072-199411000-00009.
Umehara F, Izumo S, Nakagawa M, Ronquillo AT, Takahashi K, Matsumuro K, Sato E, Osame M: Immunocytochemical analysis of the cellular infiltrate in the spinal cord lesions in HTLV-I-associated myelopathy. J Neuropathol Exp Neurol. 1993, 52: 424-430. 10.1097/00005072-199307000-00010.
Umehara F, Izumo S, Ronquillo AT, Matsumuro K, Sato E, Osame M: Cytokine expression in the spinal cord lesions in HTLV-I-associated myelopathy. J Neuropathol Exp Neurol. 1994, 53: 72-77. 10.1097/00005072-199401000-00009.
Moritoyo T, Reinhart TA, Moritoyo H, Sato E, Izumo S, Osame M, Haase AT: Human T-lymphotropic virus type I-associated myelopathy and tax gene expression in CD4+ T lymphocytes. Ann Neurol. 1996, 40: 84-90. 10.1002/ana.410400114.
Umehara F, Okada Y, Fujimoto N, Abe M, Izumo S, Osame M: Expression of matrix metalloproteinases and tissue inhibitors of metalloproteinases in HTLV-I-associated myelopathy. J Neuropathol Exp Neurol. 1998, 57: 839-849. 10.1097/00005072-199809000-00005.
Copeland KF, Heeney JL: T helper cell activation and human retroviral pathogenesis. Microbiol Rev. 1996, 60: 722-742.
Uchiyama T: Human T cell leukemia virus type I (HTLV-I) and human diseases. Annu Rev Immunol. 1997, 15: 15-37. 10.1146/annurev.immunol.15.1.15.
Itoyama Y, Minato S, Kira J, Goto I, Sato H, Okochi K, Yamamoto N: Spontaneous proliferation of peripheral blood lymphocytes increased in patients with HTLV-I-associated myelopathy. Neurology. 1988, 38: 1302-1307. 10.1212/WNL.38.8.1302.
Nakamura T, Nishiura Y, Ichinose K, Shirabe S, Tsujino A, Goto H, Furuya T, Nagataki S: Spontaneous proliferation of and cytokine production by T cells adherent to human endothelial cells in patients with human T-lymphotropic virus type I-associated myelopathy. Intern Med. 1996, 35: 195-199. 10.2169/internalmedicine.35.195.
Li Q, Verma IM: NF-kappaB regulation in the immune system. Nat Rev Immunol. 2002, 2: 725-734. 10.1038/nri910.
Vartanian T, Li Y, Zhao M, Stefansson K: Interferon-gamma-induced oligodendrocyte cell death: implications for the pathogenesis of multiple sclerosis. Mol Med. 1995, 1: 732-743.
Yamamoto K, Utsunomiya A, Tobinai K, Tsukasaki K, Uike N, Uozumi K, Yamaguchi K, Yamada Y, Hanada S, Tamura K: Phase I study of KW-0761, a defucosylated humanized anti-CCR4 antibody, in relapsed patients with adult T-cell leukemia-lymphoma and peripheral T-cell lymphoma. J Clin Oncol. 2010, 28: 1591-1598. 10.1200/JCO.2009.25.3575.
Osame M: Review of WHO Kagoshima meeting and diagnostic guidelines for HAM/TSP. 1990, New York: Raven Press
Lee B, Tanaka Y, Tozawa H: Monoclonal antibody defining tax protein of human T-cell leukemia virus type-I. Tohoku J Exp Med. 1989, 157: 1-11. 10.1620/tjem.157.1.
Saito M, Matsuzaki T, Satou Y, Yasunaga J, Saito K, Arimura K, Matsuoka M, Ohara Y: In vivo expression of the HBZ gene of HTLV-1 correlates with proviral load, inflammatory markers and disease severity in HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP). Retrovirology. 2009, 6: 19-10.1186/1742-4690-6-19.
This study was supported by grant 21590512 and 24590556 from the Japan Society for the Promotion of Science (JSPS), the Research Grant on Intractable Disease (H22-013 and H23-126) form the Ministry of Health, Labour and Welfare of Japan, and the Novartis Foundation (Japan) for the Promotion of Science.
The authors declare that they have no competing interests.
MS designed and performed the experiments, analyzed the data, and wrote the paper; TM, SI, TT, YO, and HT provided clinical samples and assembled clinical database; RT, SA, FU, and SI performed experiments, analyzed and interpreted data; YT made contribution to the conception and design of the study. All authors read and approved the final manuscript.