Narrow-band (312 nm) ultraviolet B light (UVB) is a new form of therapy for psoriasis, but its mechanism of action is unknown. In a bilateral comparison clinical study, daily exposure of psoriatic plaques to broad-band UVB (290–320 nm) or 312-nm UVB depleted T cells from the epidermis and dermis of psoriatic lesions. However, 312-nm UVB was significantly more depleting in both tissue compartments. To characterize the mechanism of T cell depletion, assays for T cell apoptosis were performed on T cells derived from UVB-irradiated skin in vivo and on T cells irradiated in vitro with 312-nm UVB. Apoptosis was induced in T cells exposed to 50–100 mJ/cm2 of 312-nm UVB in vitro, as measured by increased binding of fluorescein isothiocyanate (FITC)–Annexin V to CD3+ cells and by characteristic cell size/granularity changes measured by cytometry. In vivo exposure of psoriatic skin lesions to 312-nm UVB for 1–2 wk also induced apoptosis in T cells as assessed by the terminal deoxynucleotidyl transferase–mediated dUTP-biotin nick end labeling (TUNEL) reaction in tissue sections, by binding of FITC–Annexin V to CD3+ T cells contained in epidermal cell suspensions, and by detection of apoptosis-related size shifts of CD3+ cells. Induction of T cell apoptosis could be the main mechanism by which 312-nm UVB resolves psoriasis skin lesions.
Psoriasis vulgaris is a chronic inflammatory skin disease characterized by infiltration of T cells and hyperproliferation of keratinocytes in focal skin areas. In clinical studies, disease-related pathology is reversed by lymphocyte-targeted drugs (1–6), whereas in xenotransplant systems, psoriasis is induced or sustained by intradermal injection of activated T cells (7, 8). Therefore, psoriasis is mediated by activated T cells. In the xenotransplant model, an epidermal hyperplasia response appears to arise from cytokines derived from T cells infiltrating into skin (7). These T cells are probably reacting to a cutaneous antigen, as clonal CD8+ T cell populations have been identified (9) and as systemic administration of the costimulation blocker, CTLA4Ig, reverses clinical and pathological disease features (6). Hence, skin infiltration by activated cutaneous lymphocyte–associated antigen–positive T cells appears to cause a complex inflammatory tissue phenotype that includes (a) the presence of several types of activated leukocytes in skin lesions—CD4+ and CD8+ T cells, neutrophils, and dendritic antigen presenting cells, (b) a diverse array of cytokines produced by activated leukocytes and keratinocytes, (c) proliferation of small blood vessels and epidermal keratinocytes, and (d) increased expression of leukocyte-trafficking adhesion molecules, e.g., intercellular adhesion molecule 1 (ICAM-1), P-selectin, E-selectin, by hyperproliferative endothelial cells or keratinocytes (10).
Ultraviolet B light (UVB, 290–320 nm) is used as a therapeutic modality for psoriasis and other inflammatory skin disorders. Recently, a new UVB source which emits mostly 311/312-nm light (narrow band [NB]-UVB)1 has been introduced for treatment of psoriasis and other inflammatory dermatoses (11–14). UVB irradiation in a variety of animal and human model systems inhibits cutaneous delayed-type hypersensitivity responses to haptens (15, 16), and its therapeutic mechanism in psoriasis has been attributed to these immunosuppressive properties. Interestingly, irradiation of psoriatic skin lesions with standard UVB light causes rapid depletion of intraepidermal T cells (17) and induction of Fas ligand on keratinocytes (18). As apoptosis is induced by in vitro UVB irradiation of T cells, or by incubation of T cells with keratinocytes expressing UVB- induced Fas ligand, it has been proposed that UVB may have immunosuppressive effects in psoriasis through induction of apoptosis in disease-mediating T cells (17, 18). Although cytotoxic effects of UVB on lymphocytes in vivo are unproven, irradiation of atopic dermatitis skin lesions with high-dose UVA (the delivered dose is ∼1,000-fold higher than for therapeutic UVB) has produced detectable apoptosis in dermal lymphocytes (19). We now report that 311/ 312-nm UVB is directly cytotoxic for T cells in vivo in psoriatic skin lesions. Furthermore, this new UVB source depletes T cells to a greater extent than broad-band (BB)- UVB from both epidermis and dermis of affected skin.
Materials And Methods
The following antibodies were used by FACSCalibur® analysis (Becton Dickinson): peridinine chlorophyll protein (PerCP)– or allophycocyanin (APC)–anti-CD3, PE–anti-CD4, FITC–anti-CD8 (Becton Dickinson), and isotype mouse IgG mAbs.
23 adult patients (16 men and 7 women) received irradiation with NB-UVB (312 nm, Philips TL01) on one vertical half of the body and BB-UVB (290–320 nm, FST72T12) on the other vertical half. Five additional patients received NB-UVB on the whole body. The minimum erythema dose for each patient was established before irradiation. On each subsequent day, NB- and BB-UVB irradiations were increased by 15% unless marked erythema developed. Treatment was terminated upon attaining clinical resolution of psoriatic lesions, typically after 4–5 wk of daily treatment (20).
Skin punch biopsies were taken from psoriatic lesions of both NB- and BB-UVB–treated sites before and after UVB treatment. Biopsies were frozen in OCT solution (Miles Diagnostic Division) for histological analysis. Unconjugated anti-CD3 mAb was applied to cryosections for 60 min at room temperature. After washing with PBS, bound antibody was visualized by the avidin-biotin complex detection system (Vectastain ABC; Vector Laboratories, Inc.) with 3-amino-9-ethylcarbazol as the chromagen. For double staining, alkaline phosphatase substrate (Vector Laboratories, Inc.) was also used. Number of CD3+ cells was counted on the image analyzer using NIH image public domain software. Detection of apoptosis in tissue sections was performed by the TUNEL (TdT-mediated dUTP-biotin nick end labeling) reaction as described (17). TdT (Amersham Pharmacia Biotech) and biotin-16-dUTP (Boehringer Mannheim) are used for this technique.
Psoriatic Epidermal Cell Suspensions.
The shave biopsies were taken from eleven patients immediately before the start of treatment and after 1 and 2 wk of treatment with NB-UVB. The tissue was washed twice with sterile PBS, incubated in PBS with 1 mg/ml gentamicin (Life Technologies) for 1 h at 4°C, washed twice in PBS, and floated in 0.5% dispase (Sigma Chemical Co.) overnight at 4°C. The epidermis was removed and teased into a cell suspension after brief trypsinization.
NB-UVB Irradiation In Vitro.
Narrow-band fluorescent UVB lamps (TL01) were used as a light source. PBMCs were prepared from heparinized venous blood of healthy volunteers by Ficoll sedimentation and then irradiated in uncovered tissue culture plates (106 cells/well) in PBS. After irradiation, they were suspended in RPMI 1640 with 5% heat-inactivated normal human serum (C-six Diagnostics, Inc.) with antibiotics.
Flow Cytometric Detection of T Cell Apoptosis.
T cell apoptosis was detected using FITC–Annexin V (AnV) staining in conjunction with a membrane integrity probe (propidium iodide [PI]). In vitro–irradiated PBMCs, or epidermal cell suspensions obtained from NB-UVB–treated psoriatic lesions, were stained with APC–anti-CD3 mAb and FITC–AnV (Kamiya Biomedical Co.). After washing, the cells were stained with PI, and fluorescence intensity was measured by a four-color FACSCalibur®.
Flow Cytometric Phenotyping of T Cells in Psoriatic Lesions.
Psoriatic epidermal cell suspensions were stained with selected mAbs. After washing with PBS/0.1% sodium azide/2% FBS, cells were fixed with PBS/3.75% formaldehyde and analyzed by flow cytometry within 1 wk. Flow cytometric analysis was done using CellQuest software (Becton Dickinson).
NB-UVB Depletes T Cells From Psoriatic Lesions More than BB-UVB.
Psoriatic plaques in 23 patients were treated daily with NB-UVB or BB-UVB in a bilateral comparison study (20). The ability of NB-UVB or BB-UVB to deplete T cells from psoriatic lesions was studied with CD3 antibodies and quantitative image analysis using immunohistochemistry (Fig. 1 A). Both forms of UVB reduced intraepidermal T cells from lesional skin, but quantitative reductions were greater with NB-UVB (96 vs. 85% reduction, P = 0.01; Fig. 1 B). Reductions in dermal CD3+ cells were also greater with NB-UVB (54 vs. 29% reduction, P < 0.01; Fig. 1, A and B). Flow cytometric analysis confirmed that rapid decreases in the number of CD3+, CD4+, and CD8+ T cell subsets in psoriatic epidermis occur during the first 2 wk of treatment (Fig. 1 C).
T Cell Apoptosis Is Induced by NB-UVB Irradiation.
To establish the mechanism of T cell depletion from psoriatic lesions by irradiation, we examined NB-UVB–treated lymphocytes for DNA fragmentation and membrane changes that typify apoptosis. TUNEL reactions showed more apoptotic cells in NB-UVB–treated psoriatic lesions compared with contralateral lesions treated with BB-UVB (Fig. 2). To confirm that apoptotic cells detected in psoriatic tissue after irradiation were T cells, we performed double staining (CD3 and TUNEL). Fig. 2 (bottom) shows a psoriatic lesion taken after 2 wk of daily NB-UVB treatment. TUNEL+ cells stain red, and CD3+ cells stain blue. Double-stained cells (indicated with arrows) were observed in the treated skin, whereas no double-positives were noted before treatment.
As detection of apoptotic cells in psoriatic epidermis is problematic using the current TUNEL method (21), we used flow cytometry to examine isolated intraepidermal CD3+ lymphocytes for (a) increased binding of AnV, a protein which binds to phosphatidyl serine that is expressed on T cell plasma membranes in early stages of apoptosis; and (b) forward scatter (FSC) and side scatter (SSC) alterations that typify cytoplasmic shrinkage and organelle compaction in T cells undergoing apoptosis. As a control for these experiments, PBMCs were irradiated with increasing amounts of NB-UVB (Fig. 3 A). Dual measurement of AnV binding and membrane integrity with PI makes it possible to distinguish early (AnV+/PI−) and late stages of apoptosis (AnV+/PI+). Hence, a flow cytometer with two lasers and four-color detection was used to simultaneously assess CD3-APC, AnV–FITC, and PI staining (PE/PerCP channels) on individual cells. As shown in Fig. 3 A, dose- and time-dependent increases in binding of AnV to T cells occurred after exposure of cells to NB-UVB ranging from 25 to 100 mJ/cm2. Cells progressed from an early stage of apoptosis (AnV+/PI−) to a late stage of apoptosis (AnV+/ PI+) during 20 h after irradiation. Analysis of FSC and SSC in CD3+ cells showed dose-dependent increases in a size-shifted population (blue). Cells in this size-shifted population are displayed as blue dots in Fig. 3 A, which indicates that size-shifted cells are mostly AnV+/PI+, or late-stage apoptotic cells.
Fig. 3 B shows analysis of T cell death in lesional epidermis from a psoriatic patient after irradiation with NB-UVB in vivo. After 2 wk of daily treatment of NB-UVB, 45% of intraepidermal T cells were AnV+ vs. 14% in unirradiated psoriatic epidermis (panels for patient 1). Cells in the early stage of apoptosis (AnV+/PI−) were increased by fourfold in this patient. The mean value of four patients is listed in Table I. As shown in panels for patient 2, we also tracked cytotoxic effects of NB-UVB on intraepidermal T cells of 11 psoriatic patients using flow cytometry with ethidium homodimer (a vital fluorescent dye) and by examining T cells for cell shrinkage (reduced FSC signal) and increased granularity (increased SSC signal), changes that occur in apoptosis (22). Using ethidium homodimer staining, increased T cell death was detected in 10 out of 11 patients, and the mean value was 19.6 ± 3.25% before treatment and 30.3 ± 4.10% after treatment (listed in Table I). Using FSC and SSC analysis, the percentage of apoptotic T cells in 11 patients was 35.7 ± 12.2% before treatment and 56.3 ± 18.5% after treatment (paired t test; P < 0.001, Table I). Hence, three independent assays (AnV binding, membrane integrity, and cell morphology assays) demonstrate cytotoxic effects of NB-UVB on a significant fraction of intraepidermal T cells.
Paradoxically, the UVB spectrum (290–320 nm) causes inflammation in irradiated skin (the sunburn reaction), whereas exposure of inflamed skin to similar amounts of UV energy resolves a number of immunologically mediated dermatoses. An action spectrum study in patients with psoriasis established that wavelengths from 290 to 300 nm produced the sunburn reaction (intense erythema and keratinocyte necrosis) but had no therapeutic benefits, whereas 313-nm UVB showed mostly therapeutic, but minimally erythemogenic potential (23). Based on this action spectrum, a fluorescent UVB source was developed for psoriasis therapy that delivers 311/312-nm (“narrow-band”) UVB (11). NB-UVB has been shown to be superior for clearing psoriasis and other inflammatory disorders compared with BB-UVB sources that emit over most of the UVB spectrum (11, 12, 24). Although BB-UVB produces a wide variety of cellular and immunosuppressive effects in skin (15, 25–29), it has been suggested that the therapeutic effectiveness in inflammatory skin disorders could be mediated by the cytotoxic effects of UVB on infiltrating lymphocytes (17). However, the only direct evidence that UV light can produce lymphocyte apoptosis in human skin comes from a study of high-dose UVA (320–400 nm) used to treat patients with atopic dermatitis (19).
Surprisingly, immune-modulating effects of 311–312-nm UVB have not been studied previously in psoriatic skin or skin lesions of other inflammatory diseases. The results of this study show that NB-UVB causes greater depletion of T cells in psoriatic tissue than BB-UVB, and establish direct cytotoxic actions of UVB on T cells infiltrating skin lesions. The in vivo results are paralleled by in vitro experiments where exposure of T cells to moderate doses of 312-nm UVB light induced rapid apoptosis. In fact, given that ∼10% of UVB energy incident on skin penetrates the epidermis, there is reasonably good agreement between doses of 312-nm UVB required to kill T cells (50–100 mJ/cm2) and therapeutic amounts of 312-nm UVB delivered to psoriatic lesions (300–1,200 mJ/cm2). The greater effectiveness of 312-nm UVB in depletion of dermal T cells is probably related to (a) somewhat deeper penetration of this wavelength in dermis compared with the composite of wavelengths present in BB-UVB sources (30, 31), and (b) the ability to deliver more Joules of UVB energy with NB-UVB sources due to a reduction in its burning potential.
These investigations do not define biochemical pathways mediating the cytotoxic or immunosuppressive effects of NB-UVB. Previous studies with BB-UVB have suggested that apoptosis of epidermal T cells might be induced by interaction of Fas on T cells and upregulated Fas ligand on irradiated keratinocytes (18). Although this mechanism could also pertain to 312-nm UVB, rapid apoptosis was produced in isolated leukocytes by direct irradiation in vitro with relatively small amounts of UVB (17, 32). Potential molecular targets of UVB in T cells include p53, which is upregulated or stabilized after UVB exposure in some cells and can potentially mediate apoptosis in the setting of UVB-induced DNA damage (33, 34), or calmodulin-dependent protein kinase II, which is activated after UVB exposure and leads to activation of AP24, 24-kD apoptotic protease (35, 36). In addition, low-dose UVB can inactivate signal transducer and activator of transcription 1 (STAT-1), a critical component of signal transduction, which then inhibits gene transcription (37, 38).
In most cases, direct irradiation of normal skin with erythemogenic amounts of UVB prevents delayed-type hypersensitivity reactions to topical sensitizers. This altered immune reactivity has been attributed to UVB-induced depletion of Langerhans cells from epidermis (39). In a prior study, therapeutic amounts of BB-UVB did not appreciably reduce the abundance of CD1a+ epidermal cells in lesional psoriatic skin (17). We detected no obvious reductions in CD1a+ cells after irradiation of psoriatic lesions with NB-UVB (data not shown). Hence, depletion of T cells from psoriatic lesions appears to be selective for a restricted set of leukocytes. Accordingly, our studies suggest that the major therapeutic mechanism of UVB light in inflammatory dermatoses is a cytotoxic effect on skin-infiltrating T cells, where the mechanism of death is most likely through apoptosis.
We thank Ms. Henrietta Carbonaro for help with immunohistochemical staining, Ms. Joan Hofmann for manuscript preparation, and Dr. Ian B. Walters and Ms. Patricia Gilleaudeau for clinical assistance.
Abbreviations used in this paper
peridinine chlorophyll protein
terminal deoxynucleotidyl transferase–mediated dUTP-biotin nick end labeling
This research was supported in part by a General Clinical Research Center Grant (M01-RR00102) from the National Center for Research Resources at the National Institutes of Health; by National Institutes of Health grant AI39214; and by grants or gifts from The Carl J. Herzog Foundation, the American Skin Association, The Carson Family Charitable Trust, Dr. James Murphy, and Jean Stein. L.H. Burack and T.R. Coven were supported as Rockefeller University Clinical Scholars from May 1996 through June 1997 and March 1997 through June 1998, respectively.
Address correspondence to James G. Krueger, Laboratory for Investigative Dermatology, The Rockefeller University, 1230 York Ave., New York, NY 10021-6399. Phone: 212-327-7730; Fax: 212-327-8232; E-mail: email@example.com