key: cord-0074009-cbd7zyse
authors: Xie, Shaobing; Fan, Ruohao; Tang, Qingping; Cai, Xiao; Zhang, Hua; Wang, Fengjun; Xie, Shumin; Gao, Kelei; Zhang, Junyi; Xie, Zhihai; Jiang, Weihong
title: Identification of Robust Biomarkers for Early Predicting Efficacy of Subcutaneous Immunotherapy in Children With House Dust Mite-Induced Allergic Rhinitis by Multiple Cytokine Profiling
date: 2022-01-12
journal: Front Immunol
DOI: 10.3389/fimmu.2021.805404
sha: 50fcdf10eb4e9998475f91a7a2df60b6af850b88
doc_id: 74009
cord_uid: cbd7zyse

BACKGROUND: Subcutaneous immunotherapy (SCIT) is an effective treatment for children with allergic rhinitis (AR), but its efficacy fluctuates among patients. There are no reliable candidate biomarkers for monitoring and predicting the response to SCIT. The present study aims to identify novel biomarkers for early predicting the efficacy of SCIT in pediatric AR patients based on multiple cytokine profiling. METHODS: We prospectively recruited 72 children with house dust mite (HDM)-induced AR who were assigned to receive SCIT. The serum samples were collected and multiple cytokine profiling was conducted by Luminex assay at baseline. All patients were followed-up for 1 year and then categorized into effective and ineffective group based on their efficacy, and levels of 48 selected cytokines were tested and compared between the two groups. The potential cytokines were further validated by enzyme-linked immunosorbent assay (ELISA) in a cohort with 54 responders and 26 non-responders. RESULTS: Sixty-nine of 72 children completed one-year follow-up schedule with 46 included in effective group and 23 in ineffective group. The results of multiple cytokine profiling showed that 15 cytokines (eotaxin, G-CSF, GM-CSF, IFN-γ, IL-12(p40), IL-13, IL-15, IL-16, IL-4, MIF, MIP-1α, RANTES, SCF, SDF-1α and VEGF) were dysregulated between effective and ineffective group (all P < 0.05). Unadjusted and adjusted multivariate analysis models highlighted that serum eotaxin, IFN-γ, IL-4 and MIF levels closely associated with the efficacy of SCIT in pediatric HDM-induced AR patients. In addition, receiver operating characteristic (ROC) curves revealed potential values of these four biomarkers in predicting the response to SCIT. Further ELISA validation results in the cohort of 80 pediatric patients demonstrated that serum eotaxin and IL-4 levels were elevated in responders while IFN-γ levels decreased in responders (all P < 0.05). ROC curves demonstrated that serum IL-4 exhibited more reliable accuracy in predicting SCIT efficacy than eotaxin and IFN-γ. CONCLUSION: Our discover–validation study suggested that cytokines including IL-4, eotaxin and IFN- γ may serve as robust biomarkers for early predicting response of SCIT in children with HDM-induced AR. These results strengthen the evidence that cytokines were associated with the response of SCIT and contributed to understand its underlying therapeutic mechanisms.

Allergic rhinitis (AR) is defined as a type I allergic disease caused by common aeroallergens such as pollen, dust mite and animal fur (1, 2) . A recent epidemiological study based on 18 major cities of China reported that up to 17.6% respondents suffered from AR, and the prevalence increased gradually (3) . Previous publications highlighted that house dust mite (HDM) was the most common allergen in perennial AR in southern regions of China (4, 5) . As a common disease, AR is also prevalent in children and affects 10% to 30% of this population in the United States and other developed countries (6, 7) . Accordingly, AR was closely associated with asthma and allergic conjunctivitis and, carried a heavy disease burden for children including attention and memory deficits, fatigue, sleep-deprived and even depression (8) (9) (10) . Currently, available patient managements for AR include allergen avoidance, medications, and allergen-specific immunotherapy (AIT), and AIT is reported to be the only approach that can alter the natural course of this clinical disorder (11, 12) . AIT can be performed by subcutaneous (SCIT) or sublingual (SLIT), and growing evidences proved that SCIT was better than SLIT in controlling allergic symptoms, improving compliance and reducing rescue medication consumption (13, 14) . Although SCIT is a suitable treatment for pediatric AR, not all children respond to this therapy, and the efficacy always fluctuates across users (15) (16) (17) . Therefore, to identify and validate potentially important laboratory predictors for SCIT response may play a pivotal role on SCIT treatment for pediatric AR patients.

Cytokines are small bioactive molecules secreted by a variety of cell types including immune cells and non-immune cells, and they are implicated in diverse pathophysiological processes such as tumor immunity, inflammation response hypoxia tolerance (18) (19) (20) . Multiple cytokine profiling based on serum or urine specimen have been widely utilized in various clinical problems to explore biomarkers for early disease detection and prognosis prediction in malignant tumor, autoimmune diseases and inflammatory diseases (21) (22) (23) . Previous studies have shown that peripheral cytokines were aberrantly expressed in AR patient and associated with its onset and/or disease severity (24, 25) . In a recent study, Liu et al (26) evaluated the association between baseline laboratory parameters (including 10 cytokines) and clinical efficacy of SLIT in children with AR, and found that serum IL-10 and IL-35 levels linked to the response of SLIT. However, few is known on cytokine profiles in children with HDM-induced AR especially with regards to SCIT, and more efforts are urgently needed to explore predictors for SCIT response based on multiple cytokine profiling.

Therefore, we hypothesized that some cytokines may serve as biomarkers predicting the SCIT response. To test this hypothesis, we asked two questions:1) what cytokines could be potentially important and 2) what cytokine are more reliable and accurate in predicting SCIT response in pediatric AR patients? To address these questions, we performed this discover and validation study and identify novel and reliable biomarkers for early predicting the efficacy of SCIT in pediatric AR patients based on multiple cytokine profiling. An overview of this study profile was showed in Figure 1 .

We prospectively recruited 72 children with moderated to severe persistent HDM-induced AR who were assigned to receive SCIT between June 2019 and August 2019 at our medical center. All HDM-induced AR patients were diagnosed by allergy specialists referring to the allergic rhinitis and its impact on asthma (ARIA) guidelines (27) . The criteria for patient selection included: 1) positive results of skin tests to Dermatophagoides farina (Der f) and/or Dermatophagoides pteronyssinus (Der p) (at least ++) and/ or s-IgE level against Der f or Der p (>0.35 IU/mL); 2) age≥6 and ≤14 years old. The patients with acute exacerbation in asthma; with vasomotor rhinitis and other nasal or sinus diseases; a history of immunotherapy; with other inflammatory or septic diseases, or autoimmune diseases; consumption of anti-allergic drugs within 4 weeks before enrollment were excluded from thus study. Serum specimens were collected before onset of SCIT, and demographic and clinical data were recorded in Table 1 . The Medical Ethics Committee of Xiangya Hospital of Central South University approved this study. All children guardians provided informed consent before the children were recruited.

The peripheral venous blood samples (5 mL from each patient) were obtained, and stored at room temperature for 1-2 hours, then the samples were centrifuged, and the supernatants were harvested and stored at -80°C for subsequent experiments. Serum multiple cytokine profiling was conducted by using multiplex assay kit (BioRad, CA, USA) according to the manufacturer's instructions, and analyzed in a MAGPIX system (Luminex). The 48-Plex kit included the following cytokines: basic fibroblast growth factor (FGF), beta-nerve growth factor (b-NGF), cutaneous T cell attracting chemokine (CTACK), eotaxin, granulocyte colony stimulating factor (G-CSF), granulocyte-macrophage colony stimulating factor (GM-CSF), growth-regulated oncogene alpha (GRO-a), hepatocyte growth factor (HGF), interferon alpha-2 (IFN-a2), IFN-g, interleukin (IL)-10, IL-12(p40), IL-12(p70), IL-13, IL-15, IL-16, IL-17, IL-18, IL-1a, IL-1b, IL-1ra, IL-2, IL-2R a, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, interferon-inducible protein 10 (IP-10), leukemia inhibitory factor (LIF), monocyte chemotactic protein 1 (MCP-1), MCP-3, macrophage colony stimulating factor (M-CSF), macrophage migration inhibitory factor (MIF), monokine induced by interferon-gamma (MIG), macrophage inflammatory protein (MIP)-1a, MIP-1b, platelet-derived growth factor (PDGF)-BB, regulated on activation in normal T-cell expressed and secreted (RANTES), stem cell factor (SCF), stem cell growth factor-beta (SCGF-b), stromal cell-derived factor-1 alpha (SDF-1a), tumor necrosis factor-alpha (TNF-a), TNF-b, tumor necrosis factor related apoptosis inducing ligand (TRAIL) and vascular endothelial cell growth factor (VEGF). All cytokines and their detection limit were shown in Table S1 . During data interpretation, cytokine values below the detection limit were imputed by utilizing robust regression on order statistics as previously described (28) .

All recruited patients were assigned to receive Novo-Helisen-Depot (NHD) allergen extracts (Allergopharma, Reinbek, Germany) which were derived from Der f and Der p at a 1:1 ratio. , and the injection interval was 4 to 6 weeks. SCIT was performed in the outpatient under the guide of allergy specialists, all children was observed for >30 minute before they leave the hospital for safety assessments. All adverse reactions were recorded during the whole visit schedule. The whole treatment course was recommended to last 3 to 5 years as previously described (29, 30) .

All participants were followed up for at least 1 year, and their symptom and drug consumption during the whole treatment were recorded. The clinical effectiveness of SCIT was judged according to the improvement of clinical symptoms and the reduction in the rescue drug consumption as our previous studies described. Briefly, symptom and medication score (SMS) was calculated as the sum of total nasal symptom score and final medication score in the previous week and recorded weekly. Patients who obtained more than 30% reduction of baseline SMS was regarded as effective, otherwise, SCIT was considered as ineffective (31, 32) .

For further confirmation of potential biomarkers in discovery cohort, another independent cohort consisting of 80 HDMinduced AR children who have been treated with SCIT for more than 1 year were enrolled. After early efficacy evaluation, 54 patients were regarded as effective and 26 patients were considered as ineffective after 1-year treatment and serum samples were harvested. The potential cytokines levels were detected by commercial enzyme-linked immunosorbent assay (ELISA) kits (Multisciences, Hangzhou, China) according to the manufacturer's instructions.

Numerical variable were described as the mean± standard deviation, Student's t-test was applied when variables distributed normally, Mann-Whitney U test was performed when data distributed non-normally. Categorical data were expressed as frequencies and percentages, and the difference was compared by utilizing Chi-square test. Logistic regression analysis and receiver operating characteristic (ROC) curves were conducted to explore factors associated with the response of SCIT and evaluate the potential values in predicting the therapeutic efficacy. All statistical analyses were performed on SPSS statistics software version19.0 (IBM, Chicago, IL, USA). For all tests, P value below 0.05 for two-side was regarded as statistically significant.

In total, 69 patients finished 1 year of visit schedule and provided complete follow-up data, and 3 patients dropped out from this study. Among these patients, 46 of them were categorized into effective group, and 23 patients were included in ineffective group. Demographic and clinical data of all participants are listed in Table 1 , and no statistic difference was observed in sex, age, body mass index (BMI), concomitant diseases rate, baseline visual analogue scale (VAS) and TNSS (all P > 0.05).

In the present study, 48 cytokines were detected in the serum samples, and their abbreviations and descriptive statistics were exhibited in Table 2 . As illustrated in Table 3 and Unadjusted and adjusted multivariate analysis results highlighted that serum eotaxin, IFN-g, IL-4 and MIF levels closely correlated with the efficacy of SCIT in pediatric AR ( Table 4) . ROC curves in Figure 3 suggested that these four biomarkers exhibited potential values in predicting the response to SCIT, and detailed parameters were displayed in Table 5 .

To further confirm the above-mentioned results, serum levels of eotaxin, IFN-g, IL-4 and MIF were measured in a validation cohort including 54 responders and 26 non-responders who have finished 1-year of SCIT. No statistic difference was found in demographic and clinical data between two groups ( Table S2) .

The serum eotaxin and IL-4 levels were significantly enhanced in effective group than in effective group, while serum IFN-g concentrations were lower in effective group (all P value < 0.05). No significant difference was observed in the serum MIF levels between two groups ( Figure 4) . Furthermore, ROC curves in Figure 5 highlighted that serum IL-4 (AUC = 0.840, P < 0.001) exhibited stronger ability in predicting the efficacy of SCIT than serum IFN-g (AUC = 0.661, P =0.020) and eotaxin (AUC = 0.681, P = 0.006), and the detailed parameters were shown in Table S3 . 

The efficacy of SCIT has been proved and widely administrated in clinical practice, but only a portion of patients benefit from this therapy (12, 14, 33, 34) .An early and appropriate method to identify the patients who more likely respond to SCIT is urgently needed to conserve resources and achieve personalized treatment. Although previous studies found several biomarkers including serum periostin (35) , specific IgE/total-IgE ratio (26) and (36), which might be associated with the efficacy of SCIT, no validated biomarkers predicting the SCIT response were available in clinical practice for patients with AR.

To address this issue, we conducted a discover-validation study with a combined application of multiplex assay and further ELISA to explore potential predictive biomarkers for the efficacy of SCIT in pediatric HDM-induced AR patients. Our principal findings include: 1) effective group of the 69 patients exhibited discriminative serum cytokines compared to ineffective group, and identified four potential predictors with high accuracy (eotaxin, IFN-g, IL-4 and MIF); 2) furthermore, serum eotaxin, IFN-g and IL-4 were validated to be predictive with reliable accuracy in a cohort of 80 patients. Taken together, these results indicated that serum eotaxin, IFN-g and IL-4 were involved in the response of SCIT and its underlying therapeutic mechanisms in pediatric HDM-induced AR patients. Eotaxin is a CC chemokine ligand (CCL) with diverse immunoreactivity, and composes of eotaxin-1 (CCL11), eotaxin-2 (CCL24), and eotaxin-3 (CCL26) (37) (38) (39) (40) . Previous studies reported that eotaxin was a pivotal mediator for promoting migration, activation and maturity of eosinophils, and high levels of eotaxin facilitated local and systemic eosinophils recruitment which were involved in the pathophysiology of various autoimmune and inflammatory diseases (41) (42) (43) . A recent publication demonstrated that plasma eotaxin concentrations were elevated in chronic rhinosinusitis patients and eotaxin-3 levels positively associated with the degree of mucosal eosinophil infiltration, which FGF, fibroblast growth factor; NGF, nerve growth factor; CTACK, cutaneous T cell attracting chemokine; G-CSF, granulocyte colony stimulating factor; GM-CSF, granulocyte-macrophage colony stimulating factor; GRO, growth-regulated oncogene; HGF, hepatocyte growth factor; IFN, interferon; IL, interleukin; IP, interferon-inducible protein; LIF, leukemia inhibitory factor; MCP, monocyte chemotactic protein; M-CSF, macrophage colony stimulating factor; MIF, macrophage migration inhibitory factor; MIG, monokine induced by interferon-gamma; MIP, macrophage inflammatory protein; PDGF, platelet-derived growth factor; RANTES, regulated on activation in normal T-cell expressed and secreted; SCF, stem cell factor; SCGF, stem cell growth factor; SDF, stromal cell-derived factor; TNF, tumor necrosis factor; TRAIL, tumor necrosis factor related apoptosis inducing ligand; VEGF, vascular endothelial cell growth factor. Bold indicates statistical significance.

suggesting eotaxin might be a major biomarker in upper airway inflammatory disease (44) . Here, we firstly revealed that eotaxin levels were over-expressed in the serum of pediatric AR patients who responded to SCIT, which suggesting serum eotaxin might be concerned with the mechanisms of SCIT in AR. As is well known, type 2 inflammation and hyperactive eosinophilic response are predominated in the pathogenesis of AR and underlie the therapeutic mechanism of SCIT (14, 34, 45) . Mechanistically, the immunotherapy has been demonstrated to regulate Th1/Th2 response balance and attenuate eosinophilic inflammation in AR, and up-regulation of Th1, regulatory B and T cells was considered prognostic (46, 47) . Additionally, accumulating evidences indicated that a high baseline levels of Th2 immune and eosinophilic inflammation were beneficial in the process of allergen-specific immune tolerance (48) (49) (50) . Therefore, we have reasons to believe that elevated serum eotaxin levels were conducive to development of immune tolerance during SCIT. Another important finding was that pediatric HDMinduced AR patients in effective group presented higher baseline serum levels of IL-4 and lower IFN-g than those in ineffective group, and serum IL-4 exhibited stronger ability in predicting the efficacy of SCIT than serum IFN-g and eotaxin. IL-4 is a typical Th2 cytokine and IFN-g is a representative Th1 cytokine, and they were widely accepted to be involved in the pathogenesis of AR (45, 51) . It was established that type-2 cytokines such as IL-4, IL-5, or IL-13 were enhanced in AR and associated with allergic symptoms, and participated in the therapeutic mechanism of pharmacotherapy and AIT (52, 53) . A recent study found that AIT could induce a decrease in CD4 + T cells and Th2 cytokine levels, and the change of cytokine levels closely related to the efficacy (54) . Growing evidences showed that allergy tolerance induction characterized by the up-regulation of Treg and Breg cells were the important references of an effective AIT (55, 56) . Regulatory cytokines secreted by Treg and Breg cells would dampen Th2 immune and eosinophilic inflammation and lead to a shift to Th1 cell response (54, 57) . Therefore, we assumed that AIT only reduced Th2 cytokine levels to a limited extent when their baseline levels were low, and an excessive level of IFN-g might contribute to a failure of Th1 blockade which suggesting a no response in AIT. Some limitations should be addressed in our study. First, this study was limited to with a relatively small sample size in single medical center with the same ethnicity, which may raise the risk of selection bias and affect the generalization. Second, there is lack of internationally consensual criteria for evaluating efficacy of SCIT. Lastly, the period of follow-up was relatively short, which may weaken the conclusions. We will continue to track the all participant, and conduct further researches to confirm our conclusions in the future.

In conclusion, this is the first discover-validation study to apply multiple cytokine profiling to explore potential biomarkers for predicting the efficacy of SCIT in pediatric HDM-induced AR patients. We identified that serum eotaxin, IL-4 and IFN-g might serve as robust biomarkers for early predicting response of SCIT in children with HDM-induced AR. These results strengthen the evidence that cytokines were associated with the response of SCIT and contributed to understand its underlying therapeutic mechanisms.

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

The studies involving human participants were reviewed and approved by The Medical Ethics Committee of Xiangya Hospital of Central South University. Written informed consent to participate in this study was provided by the participants' legal guardian/next of kin.

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ShaX and RF wrote the manuscript. QT and XC performed data analysis. HZ, FW, and ZX collected sample. KG, ShuX and JZ provided statistical support. WJ designed the research study. All authors reviewed the manuscript and approved the final version. 

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2021.805404/ full#supplementary-material Conflict of Interest: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.