Abstract Regulatory T cell (Treg) impairment is implicated in the pathogenesis of chronic inflammatory diseases, but relatively little is known about the therapeutic potential of Treg restoration. Here we present clinical evidence for the Treg-selective interleukin-2 receptor agonist rezpegaldesleukin (REZPEG) in two randomized, double-blind, placebo-controlled Phase 1b trials in patients with moderate-to-severe atopic dermatitis (AD) ([58]NCT04081350) or chronic plaque psoriasis (PsO) ([59]NCT04119557). Key inclusion criteria for AD included an Eczema Area and Severity Index (EASI) score ≥ 16 and a validated Investigator Global Assessment for Atopic Dermatitis (vIGA-AD) ≥ 3, and for PsO included a Psoriasis Area and Severity Index (PASI) score of ≥ 12 and a static Physician’s Global Assessment (sPGA) score of ≥ 3. REZPEG is safe and well-tolerated and demonstrates consistent pharmacokinetics in participants receiving subcutaneous doses of 10 to 12 µg/kg or 24 µg/kg once every 2 weeks for 12 weeks, meeting the primary and secondary objectives, respectively. AD patients receiving the higher dose demonstrate an 83% improvement in EASI score after 12 weeks of treatment. EASI improvement of ≥ 75% (EASI-75) and vIGA-AD responses are maintained for 36 weeks after treatment discontinuation in 71% and 80% of week 12 responders, respectively. These exploratory clinical improvements are accompanied by sustained increases in CD25^bright Tregs. REZPEG thus represents a homeostatic approach to cutaneous disease therapy and holds clinical potential in providing long-term, treatment-free disease control. Subject terms: Skin diseases, Randomized controlled trials, Interleukins, Regulatory T cells __________________________________________________________________ Impaired interleukin-2 production and regulatory T cell dysfunction is implicated in multiple autoimmune diseases. Here, in two phase lb trials, the authors show that rezpegaldesleukin, a Treg-selective pegylated IL-2, is safe and improves symptoms in patients with atopic dermatitis or psoriasis. Introduction Inflammatory cutaneous conditions represent the largest class of chronic skin diseases and cause major health burdens and deterioration of quality of life in association with various comorbidities^[60]1–[61]5. Among the most common T cell-driven inflammatory skin disorders, atopic dermatitis (AD) and psoriasis (PsO) collectively affect up to 10% of adults globally^[62]6,[63]7. AD is classically viewed as a predominantly T helper type 2 (Th2)-skewed inflammatory disease, with PsO displaying a Th1/Th17 dominance^[64]8. Recently developed biologic therapies successfully target the specific immune pathways dysregulated in each disease: interleukin (IL)−4 or IL-13 in AD^[65]9,[66]10 and tumor necrosis factor alpha (TNFα), IL-17 or IL-12/IL-23 antagonists in PsO^[67]11–[68]13, with Janus kinase (JAK) inhibitors also approved for both indications^[69]14,[70]15. While these immunosuppressive drugs represent undisputed advancements in treatment, challenges remain, including unpredictable or incomplete responses, adverse events, and chronic relapse^[71]16. Regulatory T cells (Tregs) hold a pivotal role in orchestrating immune homeostasis through their ability to modulate the activity of Th1, Th2, and Th17 effector subsets^[72]17,[73]18, but are impaired in both PsO and AD^[74]19–[75]21. Interleukin-2 (IL-2) plays a role in controlling the proliferation and survival of Tregs^[76]22, with low dose IL-2 shown to partially rescue Treg function and provide clinical benefit in autoimmune diseases^[77]23–[78]25. However, low-dose IL-2 has limited therapeutic practicality, with shortcomings including a narrow therapeutic window and short half-life, requiring more frequent dosing that could result in conventional T cell (Tcon) induction^[79]26. Rezpegaldesleukin (REZPEG) is an IL-2 receptor (IL-2R) pathway agonist designed to stimulate the expansion and function of Tregs. It utilizes the approved recombinant human IL-2 (rhIL-2) aldesleukin sequence with stable, covalently attached polyethylene glycol (PEG) moieties which extends the half-life and confers a selectivity for Treg stimulation over Tcons compared with rhIL-2^[80]27,[81]28. We have previously shown that REZPEG effectively expands Treg populations in preclinical animal models as well as in healthy volunteers and patients with systemic lupus erythematosus (SLE)^[82]27,[83]28. Six-week treatment with REZPEG led to a rapid, dose-dependent improvement in the Cutaneous Lupus Erythematosus Disease Area and Severity Index-Activity (CLASI-A) score, encouraging the application of REZPEG to other T cell-driven cutaneous diseases. Here, hypothesizing that REZPEG may provide benefit in inflammatory skin diseases by therapeutic restoration of the Treg compartment, we apply preclinical experimental models and report the results from two randomized, double-blind, placebo-controlled Phase 1b studies in patients with moderate-to-severe PsO ([84]NCT04119557) or AD ([85]NCT04081350). REZPEG is safe and well tolerated and demonstrates consistent pharmacokinetics in both patient populations. Patients receiving REZPEG in either disease setting demonstrate clinical improvement as assessed by exploratory physician-assessed and patient-reported disease outcomes at the end of treatment at week 12 that are maintained for an additional 36 weeks. REZPEG holds great promise for cutaneous disease therapy through its novel mechanism of Treg restoration. Results REZPEG induces antigen-specific immune tolerance in mouse skin Keyhole limpet hemocyanin (KLH) delayed-type hypersensitivity (DTH) in mice is a classic preclinical model of cell-mediated immunity and was used to establish a basis for REZPEG-mediated activity in inflammatory skin diseases. Pilot pharmacological studies showed that REZPEG doses between 0.003 and 0.3 mg/kg administered subcutaneously (SC) reduced DTH response as measured by ear thickness 24 to 96 hours after KLH challenge in a dose-dependent manner compared to vehicle (Supplementary Fig. [86]1a). A follow-on mouse DTH study using sensitization and challenge with multiple antigens was conducted to evaluate the antigen-specific effects of REZPEG during and after administration (Supplementary Fig. [87]1b). In the first period, mice were sensitized and challenged with KLH in the presence or absence of REZPEG. As established in the pilot studies, ongoing treatment with 0.1 mg/kg REZPEG potently suppressed ear inflammation (Supplementary Fig. [88]1c). One month later, the same mice were sensitized with a new antigen, Ovalbumin (OVA), without any additional REZPEG treatment and challenged five days later with the new antigen OVA and the original antigen KLH (Supplementary Fig. [89]1b, Second Period). Mice that were treated with 0.1 mg/kg REZPEG in the primary efficacy period demonstrated reduced DTH ear thickness compared to vehicle when re-challenged with KLH but not with OVA (Supplementary Fig. [90]1d). The antigen-specific protection against the DTH reaction in REZPEG animals was detectable within 24 hours and was durable through 168 hours after KLH re-challenge, suggesting that REZPEG induces long-lived antigen-specific immune tolerance that lasts well beyond the end of dose administration. Patient disposition, baseline demographics, and disease characteristics Thirty patients diagnosed with chronic plaque PsO and 48 patients with moderate-to-severe AD were enrolled in two multi-center, double-blind, placebo-controlled phase 1b randomized clinical trials (Fig. [91]1, CONSORT diagrams, and Supplementary Data [92]1 and Supplementary Data [93]2 for protocols). Subcutaneous doses of 10 µg/kg and 24 µg/kg were selected for these studies based on previous phase 1 studies of REZPEG in healthy adult volunteers that demonstrated this dose range to be safe and selectively induce Tregs but not Tcons^[94]28. Enrollment was paused due to the COVID-19 pandemic and resumed only at the higher dose level for PsO, limiting analyses due to fewer placebo patients enrolled than originally planned. In the lower dose AD cohort, enrollment resumed at 12 µg/kg. Data from the 10 µg/kg cohorts are included only for the demographic and safety analyses due to the small sample sizes for these groups (n = 3 and n = 1 for PsO and AD, respectively). In each study, baseline demographics were similar across cohorts (Table [95]1). REZPEG or placebo was administered SC every 2 weeks through week 12, with post-treatment follow-up visits continuing through week 19, and extended visits for week 19 responders continuing through week 48. The study designs and patient completion information for PsO and AD are summarized in Supplementary Figs. [96]2 and [97]3, respectively. Fig. 1. CONSORT diagrams. [98]Fig. 1 [99]Open in a new tab a CONSORT diagram for Phase 1b trial of REZPEG in PsO patients. b CONSORT diagram for Phase 1b trial of REZPEG in AD patients. AD atopic dermatitis, AE adverse event, GCP Good Clinical Practice, ISR injection site reaction, PsO psoriasis. Table 1. Demographic and clinical characteristics of the patient populations at baseline Atopic Dermatitis Psoriasis Pooled 10 μg/kg 12 μg/kg 24 μg/kg Pooled 10 μg/kg 24 μg/kg Placebo REZPEG REZPEG REZPEG Placebo REZPEG REZPEG n = 10 n = 1 n = 16 n = 17 n = 5 n = 3 n = 21 Age, mean (SD), years 42.5 (19.8) 27.0 (N/A) 47.9 (17.5) 37.5 (16.4) 42.6 (15.1) 47.0 (11.3) 47.5 (13.4) Sex, n (%) Female 6 (60.0) 1 (100.0) 11 (68.8) 7 (41.2) 2 (40.0) 0 9 (42.9) Male 4 (40.0) 0 5 (31.3) 10 (58.8) 3 (60.0) 3 (100.0) 12 (57.1) Race, n (%) American Indian or Alaska Native 0 0 0 0 0 0 1 (4.8) Asian 1 (10.0) 0 2 (12.5) 0 0 0 3 (14.3) Black or African American 3 (30.0) 0 3 (18.8) 3 (17.6) 0 0 2 (9.5) White 6 (60.0) 1 (100.0) 11 (68.8) 14 (82.4) 5 (100.0) 3 (100.0) 14 (66.7) Other 0 0 0 0 0 0 1 (4.8) Ethnicity, n (%) Hispanic or Latino 0 0 3 (18.8) 7 (41.2) 0 0 2 (9.5) Not Hispanic or Latino 10 (100.0) 1 (100.0) 13 (81.3) 10 (58.8) 5 (100.0) 3 (100.0) 19 (90.5) Weight, mean (SD), kg 81.1 (22.5) 74.8 (N/A) 81.3 (18.5) 81.6 (20.6) 83.6 (12.2) 89.3 (18.5) 87.9 (18.6) BMI, mean (SD), kg/m^2 28.2 (7.5) 25.0 (N/A) 29.4 (5.4) 28.7 (5.5) 29.8 (4.9) 26.8 (5.2) 31.2 (6.2) EASI, mean (SD) 23.7 (7.1) 27.1 (N/A) 23.5 (11.2) 21.9 (5.1) --- --- --- vIGA-AD, n (%) Moderate 5 (50.0) 1 (100.0) 9 (56.3) 11 (64.7) --- --- --- Severe 5 (50.0) 0 7 (43.8) 6 (35.3) --- --- --- POEM, mean (SD) 21.2 (5.7) 25.0 (N/A) 20.0 (5.2) 19.6 (7.0) --- --- --- DLQI, mean (SD) 13.0 (5.9) 9.0 (N/A) 12.4 (6.7) 11.3 (7.2) --- --- --- BSA, mean (SD), m^2 39.0 (21.6) 31.0 (N/A) 33.8 (20.1) 33.5 (15.8) 39.6 (21.0) 22.0 (5.3) 27.7 (17.4) Itch NRS, mean (SD) 8.5 (1.3) 8.0 (N/A) 7.8 (2.1) 7.4 (2.5) 6.2 (3.0) 8.3 (1.2) 7.9 (1.9) PASI, mean (SD) --- --- --- --- 27.1 (11.9) 17.6 (2.9) 19.2 (6.6) PGA, mean (SD) --- --- --- --- 4.2 (1.3) 3.3 (0.6) 4.5 (0.9) Target lesion TSS, mean (SD) --- --- --- --- 7.6 (1.5) 6.3 (0.6) 7.6 (1.1) [100]Open in a new tab BMI body mass index, BSA body surface area, DLQI Dermatology Life Quality Index, EASI Eczema Area and Severity Index, NRS numeric rating scale, PASI Psoriasis Area and Severity Index, PGA Patient's Global Assessment of Disease Severity, POEM Patient-Oriented Eczema Measure, SD standard deviation, sPGA static Physician's Global Assessment, TSS Total Sign Score, vIGA-AD validated Investigator Global Assessment for Atopic Dermatitis. Primary endpoints addressing safety and tolerability Treatment-emergent adverse events (TEAEs) were reported by 17 (70.8%) PsO patients and 23 (67.7%) AD patients. All TEAEs were of mild or moderate severity except one involving PsO exacerbation in the 24 µg/kg group (Table [101]2). There were no serious adverse events (SAEs) related to REZPEG administration in either study. In the AD placebo group, 2 patients experienced SAEs, with cellulitis and tenosynovitis in one of these patients judged to be related to treatment, and a staphylococcal infection in the other patient unrelated to treatment. Both patients recovered, the study treatment (placebo) was not withdrawn, and the participants continued in the study. No deaths occurred in either trial. The incidence of TEAEs was similar between AD groups, reported in 8 (80%) patients receiving placebo, 10 (62.5%) receiving 12 µg/kg REZPEG, and 13 (76.5%) receiving 24 µg/kg REZPEG, and was similar in PsO (14 [66.7%] patients in the 24 µg/kg REZPEG group) (Table [102]2). Injection site reactions (ISRs) were the most common REZPEG-related findings reported in both trials (Table [103]2) with erythema being the most common feature that was self-resolving. No clinically meaningful changes in laboratory values, vital signs, or electrocardiogram were reported during either study. Table 2. Summary of treatment-emergent adverse events Atopic Dermatitis Psoriasis Pooled 10 μg/kg 12 μg/kg 24 μg/kg Overall Pooled 10 μg/kg 24 μg/kg Overall Placebo REZPEG REZPEG REZPEG REZPEG Placebo REZPEG REZPEG REZPEG Adverse Event Category, n (%) n = 10 n = 1 n = 16 n = 17 n = 34 n = 5 n = 3 n = 21 n = 24 Any TEAE 8 (80.0) 0 10 (62.5) 13 (76.5) 23 (67.6) 0 3 (100) 14 (66.7) 17 (70.8) Severe TEAEs 3 (30.0) 0 0 0 0 0 0 1 (4.8) 1 (4.2) SAEs 2 (20.0) 0 0 0 0 0 0 0 0 TEAEs related to treatment 3 (30.0) 0 2 (12.5) 5 (29.4) 7 (20.6) 0 1 (33.3) 10 (47.6) 11 (45.8) TEAEs leading to discontinuation of study 0 0 1 (6.3) 3 (17.6) 4 (11.8) 0 0 4 (19.0) 4 (16.7) All deaths 0 0 0 0 0 0 0 0 0 Adverse events in at least 5% of patients in the overall REZPEG group^a Infections and infestations 2 (20.0) 0 7 (43.8) 7 (41.2) 14 (41.2) 0 1 (33.3) 6 (28.6) 7 (29.2) Coronavirus infection 0 0 2 (12.5) 2 (11.8) 4 (11.8) N/A N/A N/A N/A Folliculitis 0 0 2 (12.5) 0 2 (5.9) N/A N/A N/A N/A Sinusitis 0 0 2 (12.5) 0 2 (5.9) N/A N/A N/A N/A Upper respiratory tract infection N/A N/A N/A N/A N/A 0 1 (33.3) 1 (4.8) 2 (8.3) Urinary tract infection 0 0 0 2 (11.8) 2 (5.9) N/A N/A N/A N/A Gastrointestinal disorders 3 (30.0) 0 1 (6.3) 3 (17.6) 4 (11.8) 0 1 (33.3) 1 (4.8) 2 (8.3) Nausea 0 0 1 (6.3) 1 (5.9) 2 (5.9) N/A N/A N/A N/A General disorders and administration site conditions 1 (10.0) 0 2 (12.5) 2 (11.8) 4 (11.8) 0 0 4 (19.0) 4 (16.7) Pain 0 0 1 (6.3) 1 (5.9) 2 (5.9) N/A N/A N/A N/A Pyrexia N/A N/A N/A N/A N/A 0 0 3 (14.3) 3 (12.5) Musculoskeletal and connective tissue disorders N/A N/A N/A N/A N/A 0 1 (33.3) 2 (9.5) 3 (12.5) Arthralgia N/A N/A N/A N/A N/A 0 1 (33.3) 1 (4.8) 2 (8.3) Investigations 0 0 0 4 (23.5) 4 (11.8) 0 0 2 (9.5) 2 (8.3) Eosinophil count increased N/A N/A N/A N/A N/A 0 0 2 (9.5) 2 (8.3) Nervous system disorders 0 0 2 (12.5) 2 (11.8) 4 (11.8) N/A N/A N/A N/A Headache 0 0 2(12.5) 0 2 (5.9) N/A N/A N/A N/A Blood and lymphatic system disorders 0 0 1 (6.3) 1 (5.9) 2 (5.9) 0 0 2 (9.5) 2 (8.3) Lymphadenopathy N/A N/A N/A N/A N/A 0 0 2 (9.5) 2 (8.3) Eye disorders 0 0 2 (12.5) 0 2 (5.9) N/A N/A N/A N/A Respiratory, thoracic and mediastinal disorders 0 0 1 (6.3) 1 (5.9) 2 (5.9) 0 0 2 (9.5) 2 (8.3) Skin and subcutaneous tissue disorders 1 (10.0) 0 1 (6.3) 1 (5.9) 2 (5.9) 0 0 3 (14.3) 3 (12.5) Injection site reactions^b 1 (10.0) 1 (100.0) 12 (75.0) 10 (58.8) 23 (67.6) 0 3 (100) 15 (71.4) 18 (75.0) [104]Open in a new tab Adverse events were coded using Medical Dictionary for Regulatory Activities (MedDRA) version 23.0 (AD) or version 22.0 (PsO). For each system organ class and preferred term, patients were included only once. Data are presented from the adjusted safety population. aN/A indicates < 5% of patients in the overall REZPEG group which includes 0. bNumber of patients with at least one injection site occurrence. AD atopic dermatitis, PsO psoriasis SAE serious adverse event, TEAE treatment-emergent adverse event. Secondary endpoints addressing pharmacokinetics After first administration in either PsO or AD patients, REZPEG was slowly absorbed into the systemic circulation with the median time to reach maximum concentration (T[max]) achieved 5 to 8 days after dosing, followed by a decline in plasma concentrations (Fig. [105]2a, b). REZPEG exposure increased in an approximately dose-proportional manner (Fig. [106]2b). The estimated geometric mean maximum concentration (C[max]) and area under the curve from dosing to the time of the last measured concentration (AUC[last]) estimates were dose-proportional in AD patients and were similar at the 24 µg/kg dose for both AD and PsO patients (Supplementary Table [107]1). Fig. 2. REZPEG-induced pharmacokinetics and pharmacodynamics. [108]Fig. 2 [109]Open in a new tab REZPEG concentration in a, PsO and b, AD patients, shown as mean ± SEM. CD25^bright Tregs measured in c, PsO and d, AD patients. CD4 + T cells in e, PsO and f, AD patients. CD8 + T cells in g, PsO and h, AD patients. All measurements performed using peripheral blood samples from patients treated with placebo (grey circles), 12 μg/kg (blue circles) or 24 μg/kg (red circles) REZPEG administered once every 2 weeks for 12 weeks. Pharmacodynamic data shown as mean fold change from baseline ± SEM. Number of samples at each time point provided in Supplementary Tables [110]6 (PsO) and 7 (AD). AD atopic dermatitis; PsO psoriasis; SEM standard error of the mean; Tcons conventional T cells; Tregs regulatory T cells. Source data are provided as a Source Data file. Exploratory endpoints addressing pharmacodynamics A dose-dependent increase in total and CD25^bright Tregs (measured either as absolute number or proportion of CD4 + T cells) was observed in REZPEG-treated cohorts (Fig. [111]2c, d, Supplementary Fig. [112]4a-d & Supplementary Fig. [113]5a-d). During the induction period, REZPEG-treated PsO patients demonstrated a respective maximum 3.1- and 15.9-fold mean change from baseline in the number of total Tregs and CD25^bright Tregs with no increases in CD4+ or CD8+ Tcons compared to placebo (Fig. [114]2e, g, Supplementary Fig. [115]5e, g). Similarly, REZPEG-treated AD patients demonstrated a maximum 1.9- and 4.0-, and 2.7- and 8.7- mean fold change from baseline in total Tregs and CD25^bright Tregs, for the 12 and 24 µg/kg dose levels, respectively, with no increases in CD4+ or CD8+ Tcons compared to placebo (Fig. [116]2f, h, Supplementary Fig. [117]5f, h). A gradual increase in the overall numbers of CD56+ natural killer (NK) cells was observed that was dose-dependent in AD (Supplementary Fig. [118]6a, b). In both PsO and AD patient peripheral blood NK cell subsets, the CD56^bright subpopulation of NK cells gradually increased as the CD56^dim subpopulation decreased over the 12-week induction period (Supplementary Fig. [119]6c-f). Exploratory endpoints addressing PsO efficacy Patients treated with REZPEG demonstrated clinical improvements in the mean percent change from baseline in the psoriasis area and severity index (PASI) score relative to placebo (Fig. [120]3). At the end of the treatment period at week 12, the REZPEG-treated patients experienced a 44.5% least-squares (LS) mean improvement from baseline in PASI score compared to a 26.2% improvement in the placebo group, with greater improvement indicated by a greater reduction (negative value) in PASI score. Patients in the REZPEG group continued to see benefit during the off-treatment period, with an LS mean 51.4% PASI score improvement from baseline at week 19 compared to 19.9% in the placebo group. A greater LS mean percent change from baseline in the target lesion Total Sign Score and body surface area (BSA) involvement was also observed in PsO patients receiving REZPEG (−51.0% and −29.4%, respectively) compared to placebo (−1.1% and −8.6%, respectively) (Supplementary Table [121]2). Improvements from baseline in patient-reported outcomes including itch numerical rating scale (NRS) and Patient’s Global Assessment of Disease Severity were numerically greater in the REZPEG group compared to placebo (Supplementary Table [122]2). Fig. 3. REZPEG efficacy in PsO patients. [123]Fig. 3 [124]Open in a new tab Reduction in PASI scores from baseline in patients with PsO after 12 weeks of 24 μg/kg REZPEG treatment (red circles) compared to placebo (grey circles) administered once every 2 weeks for 12 weeks. Data shown as mean percent change from baseline ± SEM. Number of subjects at each time point shown in Supplementary Table [125]8. PASI, psoriasis area and severity index; PsO, psoriasis; SEM, standard error of the mean. Source data are provided as a Source Data file. Exploratory endpoints addressing AD efficacy during the induction period Dose-dependent improvements in measures of overall disease severity and quality of life, as measured by Eczema Area and Severity Index (EASI) score, BSA involvement, Dermatology Life Quality Index (DLQI) and Patient-Oriented Eczema Measure (POEM) scores, were observed as early as 2-4 weeks after treatment initiation (within the first and second dose administrations) and continued through the induction period (Figs. [126]4a, b, and [127]6a, b). At week 12, the LS mean percent change in EASI score from baseline was significantly greater for patients in the 24 µg/kg group (-83.0%, p = 0.002) than those receiving placebo (-47.2%) (Table [128]3, Fig. [129]4a), with greater improvement indicated by a greater reduction (negative value) in scores. Treatment with 24 µg/kg REZPEG resulted in significant decreases in skin involvement as measured by LS mean percent change from baseline in affected BSA (-73.1%, p = 0.019) versus the placebo group (-36.4%) (Table [130]3, Fig. [131]4b). Compared to placebo, a greater proportion of those in the 24 µg/kg group achieved a validated Investigator Global Assessment for Atopic Dermatitis (vIGA-AD) score of 0 or 1 with a 2-point or more improvement from baseline to week 12 (Table [132]3). REZPEG groups also had a higher proportion of patients reporting a 4-point or more improvement in POEM scores (24 µg/kg, 64.7%; 12 µg/kg, 50.0%) or DLQI scores (24 µg/kg, 75.0%; 12 µg/kg, 46.2%) versus placebo (30.0%) at week 12. Similar 24 µg/kg REZPEG treatment differences compared to placebo were also seen at week 12 in the LS mean percent change from baseline in vIGA-AD (-26.3, p = 0.053), itch NRS (-33.4, p = 0.041), POEM (-35.4, p = 0.057) and DLQI (-65.1, p = 0.008) scores (Table [133]3). Fig. 4. AD investigator-assessed efficacy outcomes. [134]Fig. 4 [135]Open in a new tab a EASI score mean % change from baseline ± SEM. b BSA score mean % change from baseline ± SEM. c, Proportion of EASI-75 patients whose EASI score decreased by at least 75% relative to baseline. d Proportion of EASI-90 patients whose EASI score decreased by at least 90% relative to baseline. e Proportion of vIGA-AD responders, patients with a post-baseline vIGA-AD score of 0 or 1 and a ≥ 2-point improvement from baseline. Red, REZPEG 24 µg/kg; blue, REZPEG 12 µg/kg; grey, placebo. For continuous endpoints using observed data (a and b), number of subjects at each time point shown in Supplementary Table [136]9. All responder data shown as % of adjusted ITT populations. BSA, body surface area; EASI, Eczema Area and Severity Index; ITT, intention to treat; NRI, non-responder imputation; SEM, standard error of the mean, vIGA-AD, Validated Investigator Global Assessment for Atopic Dermatitis. Source data are provided as a Source Data file. Fig. 6. AD patient-reported outcomes. [137]Fig. 6 [138]Open in a new tab a DLQI mean % change from baseline ± SEM. b POEM mean % change from baseline ± SEM. c, Proportion with post-baseline DLQI score reduced by ≥ 4 points among patients with baseline score ≥ 4. d Proportion with post-baseline POEM score reduced by ≥ 4 points among patients with baseline score ≥ 4. e Proportion with post-baseline itch NRS scale reduced by ≥ 4 points among patients with baseline score ≥ 4. Red, REZPEG 24 µg/kg; blue, REZPEG 12 µg/kg; grey, placebo. For continuous endpoints using observed data (a and b), number of subjects at each time point shown in Supplementary Table [139]9. All responder data shown as % of adjusted ITT populations. DLQI, Dermatology Life Quality Index; ITT, intention to treat; NRI, non-responder imputation; NRS, numeric rating scale; POEM Patient-Oriented Eczema Measure; SEM standard error of the mean. Source data are provided as a Source Data file. Table 3. AD exploratory efficacy outcomes at week 12 Pooled 12 μg/kg 24 μg/kg n Placebo REZPEG REZPEG EASI % change from baseline, (SEM) 7, 12, 12 -47.2 (8.72) -65.1 (6.57) −83.0 (6.38) Treatment difference (95% CI) --- -17.9 (-40.13, 4.38) -35.8 (-57.78, -13.76) p-value 0.112 0.002 BSA % change from baseline, (SEM) 7, 12, 12 -36.4 (12.0) -52.8 (8.90) -73.1 (8.66) Treatment difference (95% CI) --- -16.4 (-46.85, 13.98) -36.7 (-66.84, -6.59) p-value 0.279 0.019 vIGA-AD % change from baseline, (SEM) 7, 12, 12 -29.7 (10.6) -40.9 (7.80) -56.0 (7.69) Treatment difference (95% CI) --- -11.2 (-56.76, -25.02) -26.3 (-71.63, -40.31) p-value 0.400 0.053 Itch NRS % change from baseline, (SEM) 7, 12, 12 -19.2 (12.5) -52.0 (9.31) -52.5 (9.25) Treatment difference (95% CI) --- -32.8 (-71.06, -32.91) -33.4 (-71.47, -33.56) p-value 0.045 0.041 POEM % change from baseline, (SEM) 7, 12, 12 -15.9 (14.5) -44.2 (10.8) -51.3 (10.5) Treatment difference (95% CI) --- -28.4 (-65.31, 8.56) -35.4 (-72.02, 1.17) p-value 0.127 0.057 DLQI % change from baseline, (SEM) 7, 12, 12 -10.9 (18.3) -46.8 (13.4) -76.1 (13.3) Treatment difference (95% CI) --- -35.8 (-82.22, 10.53) -65.1 (-111.41, -18.84) p-value 0.125 0.008 EASI-50, n (%) 10, 16, 17 3 (30.0) 11 (68.8) 12 (70.6) Treatment difference --- 38.8 40.6 EASI-75, n (%) 10, 16, 17 2 (20.0) 4 (25.0) 7 (41.2) Treatment difference --- 5.00 21.2 EASI-90, n (%) 10, 16, 17 2 (20.0) 2 (12.5) 4 (23.5) Treatment difference --- -7.50 3.50 vIGA-AD^a, n (%) 10, 16, 17 2 (20.0) 3 (18.8) 5 (29.4) Treatment difference --- -1.20 9.40 Itch NRS^b, n (%) 10, 15, 15 4 (40.0) 8 (53.3) 7 (46.7) Treatment difference --- 13.3 6.70 POEM^c, n (%) 10, 16, 17 3 (30.0) 8 (50.0) 11 (64.7) Treatment difference --- 20.0 34.7 DLQI^d, n (%) 10, 13, 16 3 (30.0) 6 (46.2) 12 (75.0) Treatment difference --- 16.2 45.0 [140]Open in a new tab A mixed model for repeated measures (MMRM) was used to generate least-squares (LS) means for percent change from baseline in continuous efficacy variables with baseline score as the covariate, treatment arm and protocol-defined visit time and their interaction as the fixed factors. Visit time is also used as repeated measure to account for within-subject variability. Differences and their p-values were derived for treatment vs placebo based on LS means. Missing data were imputed with NRI for categorical endpoints. 10 ug/kg REZPEG group data were not included due to small sample size. BSA; body surface area; CI, confidence interval; DLQI, Dermatology Life Quality Index; EASI, Eczema Area and Severity Index; EASI-50, patients with a 50% decrease in EASI score; EASI-75, patients with a 75% decrease in EASI score; EASI-90, patients with a 90% decrease in EASI score; LS, least-squares; MMRM, Mixed Model for Repeated Measures; NRI, non-responder imputation; NRS, numeric rating scale; PBO, placebo; POEM, Patient-Oriented Eczema Measure; SEM, standard error of the mean; vIGA-AD, Validated Investigator Global Assessment for Atopic Dermatitis. aPatients with post-baseline vIGA-AD scores of 0 or 1, with ≥ 2-point improvement from baseline. bProportion with post-baseline itch scale reduced by ≥ 4 points among patients with baseline score ≥ 4. cProportion with post-baseline POEM score reduced by ≥ 4 points among patients with baseline score ≥ 4. dProportion with post-baseline DLQI score reduced by ≥ 4 points among patients with baseline score ≥ 4. Exploratory endpoints addressing AD post-treatment efficacy outcomes Improvements in disease severity as measured by EASI score and BSA involvement observed at the end of the 12-week induction period were maintained in both REZPEG groups through week 19 (Fig. [141]4a, b). To evaluate sustained responses beyond the initial follow-up period, patients in all cohorts meeting the established minimal clinically important difference (MCID) of 50% improvement from baseline in EASI score (EASI-50)^[142]29 at week 19 were followed through an extended efficacy period from week 19 through week 48 or until EASI-25 response was no longer met. For these long-term responders, disease improvements in EASI score were largely sustained through week 48. Of the week 19 EASI-50 responders, the proportion who maintained their EASI-50 responses through week 48 were 7/10 (70%) and 3/9 (33.3%) for the 24 µg/kg and 12 µg/kg groups, respectively, compared to 0/3 (0%) in the placebo group (Fig. [143]5a). Fig. 5. AD off-treatment extended efficacy outcomes through week 48. [144]Fig. 5 [145]Open in a new tab Proportion of week 19 EASI-50 responders maintaining a, EASI-50, decrease in EASI score by at least 50% relative to baseline; b, EASI-75, decrease in EASI score by at least 75% relative to baseline; c, EASI-90, decrease in EASI score by at least 90% relative to baseline; d, vIGA-AD score of 0 or 1 and a ≥ 2-point improvement from baseline; e DLQI score reduction by ≥ 4 points among patients with baseline score ≥ 4. f POEM score reduction by ≥ 4 points among patients with baseline score ≥ 4. g itch NRS score reduction by ≥ 4 points among patients with baseline score ≥ 4. Red, REZPEG 24 µg/kg; blue, REZPEG 12 µg/kg; grey, placebo. DLQI, Dermatology Life Quality Index; NRI, non-responder imputation; NRS, numeric rating scale; POEM, Patient-Oriented Eczema Measure; vIGA-AD, Validated Investigator Global Assessment for Atopic Dermatitis. Source data are provided as a Source Data file. Similarly, EASI-75 response rates were maintained during the off-drug follow-up from weeks 12 to 19, with the proportion of responders in the REZPEG groups (24 µg/kg, 52.9%; 12 µg/kg, 31.3%) remaining higher than in the placebo group (10.0%) at week 19 (Fig. [146]4c) and sustained through week 48 (Fig. [147]5b). Week 19 responders achieving a 90% improvement in EASI score (EASI-90) responders were numerically greater in the 24 µg/kg REZPEG group (29.4%) compared to placebo (10.0%) (Fig. [148]4d), and of the 5/10 (50%) of patients entering the extended follow-up period with EASI-90, 4 patients (80%) maintained their EASI-90 responses at week 48 (Fig. [149]5c). The proportion of vIGA-AD responders at week 19 was also higher in the 24 µg/kg REZPEG group (35.3%) versus placebo (10.0%, Fig. [150]4e), with similar rates maintained through week 48 (Fig. [151]5d). Altogether, across the key investigator-assessed efficacy endpoints in the 24 µg/kg REZPEG group, durable off-treatment responses were observed in EASI-75 (71.4%), EASI-90 (100%), and vIGA-AD (80%) (Supplementary Table [152]3). In stark contrast, patients in the placebo group experienced higher off-treatment relapse rates in the extended efficacy period compared to REZPEG treatment groups, with the loss of measurable benefit in all efficacy outcomes well before week 48 (Fig. [153]5). Improvements observed in patient-reported disease outcomes through the 12-week induction period were also maintained during the initial follow-up period from weeks 12 to 19 and continued through week 48. After discontinuing treatment, DLQI and POEM percent change from baseline were sustained in both REZPEG treatment groups (Fig. [154]6a, b, respectively). DLQI response rates remained numerically higher in the 24 µg/kg REZPEG group (62.5%) compared to placebo (30.0%) at week 19 (Fig. [155]6c) and were durable in long-term responders through week 48 (Fig. [156]5e). The percentage of POEM responders also remained high at week 19 after discontinuing treatment at week 12, with the proportion of patients with a 4-or-more-point reduction in POEM score from baseline greater in the 24 µg/kg REZPEG group (64.7%) compared to placebo (20.0%, Fig. [157]6d). All patients in the 24 µg/kg REZPEG group entering the long-term follow-up period at week 19 were POEM responders, with responses sustained in 70% of these patients through week 48 (Fig. [158]5f). REZPEG treatment groups also showed sustained improvements in itch NRS response rates at week 19 (24 µg/kg, 46.7%; 12 µg/kg, 40.0%) compared to placebo (0.0%) (Fig. [159]6e), with response rates maintained through 48 weeks (Fig. [160]5g). Notably, for patients in the 24 µg/kg REZPEG group who at week 12 achieved an itch NRS (n = 7), POEM (n = 11), and DLQI (n = 12) response, 71.4%, 63.6%, and 41.7%, respectively, maintained their responses through 48 weeks (Supplementary Table [161]3). Serum proteomic biomarkers A proteomics analysis was conducted to investigate REZPEG’s biomolecular mechanisms beyond Treg cellular pharmacodynamics. The Olink proteomics platform was used to measure 1461 soluble serum proteins from AD patients treated with REZPEG or placebo at baseline and throughout the induction period on weeks 2, 3, 4, and 12 (Supplementary Table [162]4). Results were analyzed using a longitudinal linear mixed effects model to identify proteins that were differentially detected in treatment versus placebo groups as a function of REZPEG dose and time on treatment. Volcano plots summarize the 328 proteins that were significantly elevated or decreased in response to REZPEG treatment relative to baseline (Fig. [163]7a), with a selection of proteins relating to AD and immunoregulatory processes further identified in Fig. [164]7b. The expression profiles of these biomarkers exhibited dose- and time-dependency of REZPEG administration over the 12-week induction period (Fig. [165]7b). To further refine their functional associations, REZPEG-modulated proteins were assessed for pathway enrichment using the Reactome knowledgebase^[166]30. The top 15 statistically significant pathways induced by REZPEG included immunoregulatory processes (interleukin, TNF superfamily, and chemokine signaling) and cellular migration/adhesion networks (integrins, extracellular matrix organization, and cell surface interactions) (Supplementary Fig. [167]7, Supplementary Table [168]5). Fig. 7. Serum proteomic biomarker analysis. [169]Fig. 7 [170]Open in a new tab a Dose-dependent volcano plots of the serum proteins showing the -log10(p-value) vs fold-change in protein expression in response to REZPEG treatment compared to placebo. Data were fitted with a linear mixed model with multiple testing correction using Benjamini-Hochberg. Statistical comparisons were made between treatment and placebo using the Tukey method. Proteins with a statistically significant treatment-based change (threshold p < 0.05) are indicated by red circles; those with non-significant changes are indicated by teal circles. b Example line charts of differentially-detected serum proteins over the 12-week REZPEG treatment induction period shown as Log2 fold change (FC) in expression from baseline ± SEM. Red, REZPEG 24 µg/kg; blue, REZPEG 12 µg/kg; grey, placebo. Number of samples at each time point provided in Supplementary Table [171]10. CCL, CC motif chemokine ligand; CD160, cluster of differentiation 160; CX3CL1, C-X3-C motif chemokine ligand 1 (fractalkine); FASLG, Fas ligand; GNLY, granulysin; IL, interleukin; ITGB2, integrin beta 2 (CD18); Log2(FC), Log2 fold change; LTA, lymphotoxin alpha; NCR1, natural cytotoxicity triggering receptor 1 (NKp46); RRM2, ribonucleotide reductase regulatory subunit M2; SEM, standard error of the mean; TNFRSF4, tumor necrosis factor receptor superfamily member 4 (CD134, OX40). Source data are provided as a Source Data file. Discussion Tregs are key to the maintenance of immunological tolerance and their deficiency has been implicated in the pathogenesis of many chronic inflammatory diseases. Agents able to induce Treg proliferation and activation have only recently been identified as clinically relevant therapies^[172]31,[173]32. We have previously shown that the novel IL-2R pathway agonist REZPEG causes a marked and selective dose-dependent increase in CD25^bright Tregs accompanied by improvements in CLASI-A score in SLE patients^[174]28. Here, we hypothesized that REZPEG could restore immunological homeostasis for the treatment of inflammatory cutaneous pathologies. Our observations in a mouse model of DTH support this rationale, demonstrating the induction of antigen-specific immune tolerance that persists for months after the completion of REZPEG treatment. Furthermore, the results presented here from the Phase 1b trials in PsO and AD patients demonstrate the capacity of REZPEG to safely and dose-dependently increase Tregs and rapidly improve measurable exploratory disease outcomes that are largely durable for at least 36 weeks after ceasing treatment, consistent with the durability of response observed in the mouse DTH studies. To our knowledge, this is the first report of a randomized clinical trial evaluating an engineered Treg-selective rhIL-2 for the treatment of patients with moderate-to-severe PsO or AD. The safety profile of REZPEG during the observational period reported here is consistent with prior studies of REZPEG^[175]28 and other clinical trials for low-dose rhIL-2^[176]23,[177]24. The overall incidence of TEAEs was similar between treatment arms in both studies. No REZPEG-treated patients reported any SAEs and there were no fatal TEAEs. Importantly, no patients experienced clinical manifestations of cytokine release syndrome or other adverse events seen with higher doses of rhIL-2 aldesleukin^[178]28, which poses risks of capillary leak syndrome, inflammatory disease, cardiac disorders, and hematologic toxicity^[179]33. In contrast to reports of a greater incidence of conjunctivitis after the use of IL-13 and/or IL-4 inhibitors^[180]34–[181]36, conjunctivitis was not observed as a side effect of REZPEG treatment in AD. REZPEG demonstrated dose-proportional pharmacokinetics and a terminal half-life consistent with previous studies^[182]28. REZPEG administration also resulted in a dose-dependent pharmacodynamic profile, with similar increases in CD25^bright Tregs observed in PsO and AD, and exceeding those observed in a recent rhIL-2 study in PsO^[183]37. CD25^bright Tregs are recognized as a Treg subpopulation with high activity and immunosuppressive capacity^[184]38. In both AD and PsO, Treg stimulation was sustained through multiple administrations of REZPEG without significant increases in Tcons at either dose level. The increases in Tregs but not Tcons in the current studies in patients with PsO and AD are consistent with prior studies of REZPEG in healthy volunteers and patients with SLE^[185]28. These results add to the growing body of evidence supporting REZPEG’s reliable Treg pharmacological profile across healthy and diseased immune systems. NK cell dysregulation is a functionally relevant feature of inflammatory skin disorders contributing to the disease process, with reduced NK cell numbers and function described in patients with PsO and AD^[186]39,[187]40. Long-term treatment with dupilumab was shown to reverse AD-associated NK cell deficiency correlated with clinical response^[188]41,[189]42, suggesting a possible therapeutic role for NK cells^[190]40. In the current study, REZPEG treatment expanded the number of NK cells in some patients at the higher doses tested, suggesting that REZPEG may also contribute to rebalancing immunity through NK cell restoration. Within the NK cell population, REZPEG decreased the CD56^dim subset of NK cells while simultaneously increasing that of CD56^bright, the latter shown to have an important immunoregulatory role through the elimination of highly proliferative, activated autoreactive CD4+ Tcons that have escaped Treg suppression^[191]43,[192]44. While Tregs are the primary cellular target of REZPEG, proteomic analysis of serial serum samples performed separately from clinical trial endpoint assessments revealed additional insights into its potential disease-modifying mechanism of action and may also shed light on new target identification strategies for drug discovery. Consistent with its biological activity as an IL-2R agonist and observed therapeutic effects, REZPEG modulated multiple immunoregulatory pathways, including those involving Treg function, immunosuppressive cytokines such as IL-10, ectodomain shedding of immunomodulatory proteins, antigen recognition and major histocompatibility complex (MHC) binding, anti-microbial pathways, cell adhesion and migration, and antagonism of Th2 polarization. We also observed modulation of known targets for AD therapy, including tumor necrosis factor receptor superfamily member 4 (TNFRSF4/OX40 receptor)^[193]45 and C-C motif chemokine ligand 22 (CCL-22)^[194]46 that binds to the C-C motif chemokine receptor 4 (CCR4)^[195]47. In addition, we observed REZPEG-induced reductions in serum proteins known to be elevated in patients with AD, including IL-15^[196]48, C-X3-C motif chemokine ligand 1 (CX3CL1/fraktalkine)^[197]49, and IL-19^[198]50. REZPEG dramatically decreased serum levels of C-X-C motif chemokine ligand 16 (CXCL16), which could contribute to its therapeutic effect in PsO, where elevated levels are known to recruit pathogenic CD8 + T cells to the site of skin lesions^[199]51. The ability of REZPEG to directly induce Treg expansion, as well as its dose-dependent reduction of IL-15 supports an interesting hypothesis linking its potential effects on tissue-resident memory T cell populations^[200]52,[201]53 to the durability of efficacy observed in the antigen challenge mouse model and in patients with AD or PsO. Work to explore the correlation between Tregs, these serum proteins, and treatment response to REZPEG during the induction period and beyond is ongoing and will be the subject of future reports. REZPEG demonstrated clinical benefit in both PsO and AD, with responses exhibiting rapid onset especially in AD. Efficacy in PsO was observed but was less robust than that seen for AD patients. This may be due to the small sample size of the PsO trial or may reflect other mechanistic differences between PsO and AD immunology. Efficacy in AD was dose-dependent and demonstrated consistency across physician-assessed and patient-reported outcomes. The magnitude of the clinical effect at the end of the induction period was notable in these patient populations and demonstrated off-treatment durability, most remarkably in AD patients. Patients receiving REZPEG at the higher dose maintained disease control for 36 weeks after discontinuing treatment and without additional systemic therapy. Relapse is a common feature of AD, with many patients requiring long-term treatments for adequate disease control. The durable responses reported suggest the possibility for infrequent maintenance dosing regimens with REZPEG, such as once every 12 weeks, to more completely prevent recrudescence of disease activity^[202]54. Durable therapies that provide benefit after treatment discontinuation remain an unmet need in AD. Studies have demonstrated that up to 79% of patients who discontinue dupilumab or JAK inhibitors lose disease control and require rescue treatement^[203]55–[204]58. Supported by the serum biomarker analysis and the observed efficacy of REZPEG in improving CLASI-A in SLE, PASI in PsO, and EASI in AD, a potential mechanism of action is proposed whereby REZPEG administration induces Treg expansion with the ability to engage multiple immunoregulatory mechanisms to facilitate immune homeostasis by attenuating Th1, Th2, and Th17 responses (Supplementary Fig. [205]8). REZPEG is uniquely poised to address a diversity of immunopathologies through a central pathway of IL-2R-driven Treg rescue. This contrasts with the majority of available pharmacological agents with narrowly targeted biological activity demonstrated in limited disease settings. Limitations of the studies included the small numbers of patients, which is a challenge inherent to all phase 1 clinical trials. Accordingly, the studies were not powered for analyses of a number of secondary efficacy endpoints or to directly compare different dose regimens. Additionally, with AD suggested to be more prevalent in adolescents than in adults, the demographics of the study population may not be reflective of the general population. In both studies, but especially in PsO, there were also fewer patients after week 19, as the long-term follow-up period through 48 weeks included only those with sustained PASI-50 or EASI-50 responses. In conclusion, treatment with REZPEG for 12 weeks caused durable dose-dependent improvements in physician-assessed disease activity and patient-reported outcomes in patients with moderate-to-severe PsO and AD. Together, the results presented here validate a role for Tregs in chronic inflammatory skin diseases. IL-2R-induced Treg proliferation and activation holds clinical potential as a key target in the AD treatment paradigm, supporting the advancement of REZPEG into a Phase 2b study in AD ([206]NCT06136741). Methods Mouse model of DTH All animal studies were conducted in compliance with India’s Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA, 2005) and per the recommendations of the Association for Assessment and Accreditation of Laboratory Animal Care International (AAALAC). The study design and methodology for studies LS-2016-924 and LS2017-900A were reviewed and permission was granted to perform the experiments by the Institutional Animal Ethics Committee of Nektar Therapeutics (India) Private Limited (IAEC/NKTI). BALB/c mice aged 6–8 weeks (N = 8 to 10 per group) were obtained through Taconic Biosciences (BALB/cAnNTac, stock number BALB-MPF-F). Female mice were used for these studies due to practicalities in animal husbandry; in all REZPEG nonclinical studies, there were no significant sex-based differences reported in toxicology, toxicokinetics, pharmacokinetics, or pharmacodynamics. Experimental and control animals were co-housed in a specific pathogen-free (SPF) facility and randomized by mean body weight on the day of the experiment. Four animals were group-housed in individually ventilated polysulfone cages. The facility had an automatically controlled light cycle of 12 hours light (0700–1900) and 12 hours dark (1900 to 0700), controlled temperature of 22 ± 3 °C, and relative humidity between 30 and 70%. The murine keyhole limpet hemocyanin (KLH)-delayed-type hypersensitivity (DTH) model was based on Engstrom et al.^[207]59. Mice receiving SC REZPEG (0.003-0.3 mg/kg in the pilot study and 0.1 mg/kg in the subsequent multi-antigen challenge study) or vehicle on days 0, 3, and 6 were sensitized with KLH (100 µg in 100 µL) prepared with Complete Freund’s Adjuvant (CFA) and Incomplete Freund’s Adjuvant (IFA) in a 1:1:1 v/v proportion administered SC between the shoulder blades on day 0. Mice were challenged with KLH (10 µg in 5 µL intradermally [ID] into ear pinna) on day 5 with ear thickness measured by Mitutoyo Thickness gauge immediately prior to challenge and 24, 48, 72, and 96 hours postchallenge. On day 30 in the multi-antigen study, animals that had been previously sensitized/challenged with KLH and treated with 0.1 mg/kg REZPEG were sensitized with Ovalbumin (OVA, 100 µg in 100 µL) prepared with CFA in a 1:1 v/v proportion administered SC between the shoulder blades. No further REZPEG treatment was given. Mice were challenged with OVA (non-specific antigen, 50 µg in 5 µL ID into ear pinna) or re-challenged with KLH (specific antigen, 10 µg in 5 µL ID into opposite ear pinna) with ear thickness measured as above. PsO and AD study designs Two multi-center, double-blind, placebo-controlled, phase 1b randomized clinical trials (PsO, [208]NCT04119557; AD, [209]NCT04081350) were designed to evaluate the safety and tolerability of multiple SC doses of REZPEG (NKTR-358, LY3471851) in patients with chronic plaque PsO or moderate-to-severe AD. The PsO study was conducted at 12 study sites within the United States between November 26, 2019 and July 21, 2021, and the AD study was conducted at 20 study sites within the US between November 18, 2019 and June 16, 2022. The studies were conducted in accordance with ethical principles of the Declaration of Helsinki, Council for International Organizations of Medical Sciences International Ethical Guidelines, applicable International Council for Harmonisation (ICH) Good Clinical Practice (GCP) Guidelines, and applicable local laws. Approvals for human subjects research and use of human material were obtained from the appropriate Institutional Review Boards (IRBs) at each study center. Protocols J1P-MC-KFAC (PsO) (Supplementary Data [210]1) and J1P-MC-KFAD (AD) (Supplementary Data [211]2) and amendments were reviewed and approved by Advarra, serving as the Central Ethics Review Board (PsO) and the IRB (AD), before the studies were initiated/amended. All participants provided written informed consent prior to participating in the trials. Compensation was provided to patients for participation in these studies. Both studies consisted of a 4-week screening period followed by a 12-week intervention period and a 7-week initial post-treatment follow-up period through week 19. Sustained responses were evaluated in PASI-50 (PsO) or EASI-50 (AD) responders during an extended follow-up period from week 19 through week 48 or until PASI-25 or EASI-25 response was no longer met. Overviews of the study designs are provided in Supplementary Fig. [212]2 (PsO) and Supplementary Fig. [213]3 (AD). The protocols are included as Supplementary Data [214]1 and Supplementary Data [215]2. The list of investigators is provided in the Acknowledgments.