Figures
Abstract
Background
Hand-food-mouth disease (HFMD) cases can be fatal. These cases develop rapidly, and it is important to predict the severity of HFMD from mild to fatal and to identify risk factors for mild HFMD. The objective of this study was to correlate the levels of serum inflammatory cytokines with HFMD severity.
Methods
This study was designed as a nested serial case-control study. The data collected included general information, clinical symptoms and signs, laboratory findings and serum cytokine levels.
Results
The levels of IL-4, IL-6, IL-10, TNF-α and IFN-γ in patients with severe HFMD were significantly higher than in mild patients during the 2nd to 5th day after disease onset. The levels of IL-4, IL-6, IL-10 and IFN-γ increased from the 2nd day to the 4th day and later decreased. The levels of TNF-α were high on the first two days and subsequently decreased. The changes of IL-10, TNF-α and IFN-γ in the controls were similar for all cases. The levels of IL-4, IL-6 and IL-17 in the controls were not significantly different with the progression of HFMD.
Citation: Duan G, Yang H, Shi L, Sun W, Sui M, Zhang R, et al. (2014) Serum Inflammatory Cytokine Levels Correlate with Hand-Foot-Mouth Disease Severity: A Nested Serial Case-Control Study. PLoS ONE 9(11): e112676. https://doi.org/10.1371/journal.pone.0112676
Editor: Lisa F. P. Ng, Singapore Immunology Network, Agency for Science, Technology and Research (A*STAR), Singapore
Received: July 14, 2014; Accepted: October 10, 2014; Published: November 12, 2014
Copyright: © 2014 Duan et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. All relevant data are within the paper and its Supporting Information files.
Funding: This study was supported by grants from National Natural Science Foundation of China (81172740) (http://isisn.nsfc.gov.cn). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Hand-foot-mouth disease (HFMD) is caused by enterovirus 71 (EV71) and coxsackievirus (CV) A16, and it continues to be a major public health issue in southeastern Asian countries and regions [1]–[4]. HFMD is typically mild and self-limiting. HFMD is most prevalent in children, almost all of whom recover within 4–6 days [5]. However, some patients may quickly develop very severe HFMD with complications, including encephalitis, encephalomyelitis, meningitis, pulmonary edema, circulatory failure, and other serious complications, even death.
Numerous studies have shed light on the etiology and epidemiology of HFMD, and have helped medical professionals and public health officials worldwide understand this condition. In recent years, several HFMD outbreaks occurred in China, Japan, Taiwan, New Zealand and Singapore [1]–[4], [6]–[9]. From May 2008 to April 2009, the China CDC reported 765,220 HFMD cases, including 4,067 severe cases and 205 deaths, with a total incidence rate of 57.9/100,000. Of these, 81.59% were severe cases and 96.43% of the deaths presented with EV71 infection. More than 80% of severe cases and all deaths occurred in 0–6 years age group, and the deaths were primarily due to severe HFMD with complications [10]. The continuing epidemic of HFMD and the potential for serious complications has evoked the highest level of attention from the Chinese government. In response, the Chinese government listed HFMD as a nationally notifiable disease since May 2008. A screening criterion for severity was also recommended according to the clinical manifestations, particularly for children younger than 3-years old. Currently, tests and biomarkers that prospectively predict the progress of HFMD have yet to be developed. Key laboratory findings as potential indicators of severity are not well known, and in particular, the host immune response during the course of the disease also remains unclear. Previous studies examined cellular cytokines in EV71 patients with different outcomes [11]; however, the dynamic changes of these cytokines during the course of disease were unclear.
Therefore, the objective of this study was to determine the risk factors of severe HFMD and to assess the relationship of T cell-related serum inflammatory cytokine levels, including interleukin (IL)-4, IL-6, IL-10, IL-17, interferon (IFN)-γ and tumor necrosis factor (TNF)-α, with the progression of HFMD and its severity.
Methods
Study subjects and design
Based on the nested case-control study postulate, our study was designed as a nested serial case-control study. All subjects from the Zhengzhou children's hospital were identified prospectively and diagnosed based on the Chinese guidelines for HFMD diagnosis and treatment (Chinese Ministry of Public Health, revised in 2010) [12]. A total of 102 patients were selected from the hospitalized children (male 62, female 40) aged 6 years and younger (age range, 6–77 months), diagnosed with HFMD during the study period of April 2012 to November 2012 if they had the onset of at least one of the following features: maculopapular or vesicular rash on the palms and/or soles and vesicles or ulcers in the mouth. They were designated prospectively as cases (65 severe cases) and controls (37 mild cases). All subjects were allocated into 4 case-control series according to their course of disease when they visited the hospital as follows: for the 2nd day, 3rd day, 4th day, and 5th day after HFMD onset, the sample size was 9, 15, 22, 19 in the case groups and 9, 9, 9, 10 in the controls, respectively. At the first hospitalized day, serum samples from all patients were obtained.
The study was reviewed and approved by the Life Sciences and Ethics Committee of Zhengzhou University and the Ethics Committee of the Zhengzhou Children's Hospital. Written informed consent was obtained from each participants parents before enrollment.
Definitions of cases and controls
The cases were defined as having severe or fatal HFMD [13], with severe neurological symptoms, such as febrile seizures, myoclonic jerks, and leg trembling, and more serious complications, including encephalitis, meningitis, acute flaccid paralysis (AFP), cardio respiratory failure, or death. Controls with mild HFMD were without any serious complications.
Measurements and data collection
The data were collected using a pre-designed structured questionnaire covering the general information, clinical symptoms and signs, laboratory findings, and other factors that may be associated with or indicate severe and fatal HFMD by trained interviewers through face-to-face interviews with the children's parents or babysitters and/or medical reports.
The serum concentrations of IL-4, IL-6, IL-10, IL-17, IFN-γ and TNF-α were measured by enzyme linked immunosorbent assay (ELISA) kits (Shanghai Joyee Biotehnics, Shanghai, China) according to the manufacturer's instructions. The detection limits of these parameters were consistent with the manufacturer's instructions. The collected stool samples were submitted for virus isolation. The samples were inoculated into human embryonic fibroblast (MRC-5), LLC-MK2, HEp-2, and rhabdomyosarcoma (RD) cell cultures. When the enteroviral cytopathic effect involved more than 50% of the cell monolayer, the cells were scraped and indirect fluorescent-antibody staining with a panenteroviral antibody (Chemicon International, Temecula, CA, USA) was performed to identify the enterovirus. These isolates were subsequently identified as EV71 by reverse-transcriptase PCR and sequencing analysis within the VP-1 region of EV71.
Statistical analysis
The database software program SPSS v. 13.0 (SPSS Inc., USA) was used for statistical analysis. Differences in the means of the continuous variables were tested using Student's t-test or Kruskal-Wallis test, depending on the validity of the normality assumption and the homogeneity of variance. For categorical variables, the proportions were compared using Fisher's exact test or the Chi-square test. A two-tailed p-value of <0.05 was considered significant. Multivariate analysis was performed to examine the adjusted odds ratio for risk factors using logistic regression. A significance level of <0.05 was used for this study.
Results
General characteristics of the participants
During the study period of April 2012 to November 2012, 102 patients with HFMD were identified, with 65 cases and 37 controls, who recovered completely with no deaths. The mean time for mild to severe HFMD was 2.51 days (±1.83 days). The mean age was 23.54 months (±13.00 months), and the male/female ratio was 1.5/1. The mean age of the controls was 22.57 months (±12.93 months), and the male/female ratio was 1.6/1. There was no significant difference between the cases and controls for age and gender (P>0.05).
Patient clinical characteristics at hospital admission are presented in Figure 1. Of the 102 patients, the most common symptoms were fever and rash (100% in cases vs. controls), followed by hypersomnia (100% in cases and 81.1% in controls). Neurological symptoms occurred in all cases, including hypersomnia (100%), myoclonic jerks (100%), leg trembling (12.3%) and febrile seizures (10.8%); whereas, no neurological symptoms were present in the controls, except 30 children (81.1%) who presented hypersomnia. Cough occurred in 9.2% cases and 11.8% controls. Of the patients, 23.1% of the cases and 5.4% of the controls were vomiting. Furthermore, of the cases, there were a greater proportion of patients with complications compared to the controls, including brainstem encephalitis (12.3% vs. 0), neurogenic pulmonary edema (1.5% vs. 0), and sepsis (13.8% vs. 8.1). However, the percentage of pneumonia/bronchitis (40.5%) in the controls was higher than in the cases.
BE = brainstem encephalitis; NPE = neurogenic pulmonary edema.
Laboratory findings
Table 1 summarizes the laboratory findings. In the cases vs. controls, laboratory values of white-blood-cell count, neutrophils, lymphocytes, red-blood cell count, hemoglobin, hematocrit, aspartate aminotransferase, acetate dehydrogenase, creatine kinase, α-hydroxybutyric acid, and C-reactive protein levels were not significantly different (P>0.05). EV71-positive samples were found in 76.9% of cases vs. 45.9% of controls (P<0.05). The degree of fever (>39°C) was 40% vs. 16.2%, duration of fever (>3 days) was 64.9% vs. 18.9, length of in-hospital stay (>5 d) was 53.8% vs. 32.4%, heart rate (>130/min) was 47.7% vs. 32.4%, and respiratory rate (>35/min) was 41.5% vs. 21.6%, for cases and controls, respectively (all P<0.05).
Multivariate analysis
To determine the relative importance of the factors associated with severity, a multivariate analysis was performed. In the logistic regression model, EV 71-positive (95% CI 1.325–11.550), degree of fever (>39°C) (95% CI 1.088–11.540), duration of fever (>3 days) (95% CI 2.204–19.664), and length of in-hospital stay (>5 d) (95% CI 1.404–12.609) were significantly associated with severity (Table 2).
T cell-related serum inflammatory cytokines' levels
Figure 2 indicates the relationships between the levels of T cell-related serum inflammatory cytokines and the course of HFMD onset between cases and controls. The following descriptions for the serum cytokines levels are as the median (P50) and quartiles (P25∼P75). The median serum levels of IL-4 in the cases were significantly higher than in the controls during the 2nd to 5th day after disease onset and were 12.98 (12.60∼13.92) vs. 9.26 (7.61∼11.11), 19.10 (18.32∼20.27) vs. 10.74 (9.81∼12.23), 23.22 (21.74∼26.02) vs. 10.74 (10.00∼12.23), and 23.02 (21.44∼25.42) vs. 10.37 (9.44∼11.02), respectively (P = 0.001 for the 2nd day, and P<0.001 for the other days). The levels of IL-4 among the cases were significantly different and increased from the 2nd day to 4th day (P<0.001). There was no significant difference in the IL-4 levels between the 4th day and 5th day (P = 0.564) among cases. The highest level of IL-4 in the cases occurred at the 4th day after disease onset. The controls were not significantly different for HFMD progression (P = 0.146). The serum levels of IL-6 of the cases were significantly higher than in the controls during HFMD from days 2 to 5 as follows: 53.22 (47.42∼63.12) vs. 21.40 (16.99∼28.16), 72.49 (56.61∼75.61) vs. 27.97 (26.42∼30.43), 65.20 (44.91∼79.52) vs. 25.71 (22.31∼29.42), and 35.70 (31.46∼43.29) vs. 24.20 (22.31∼26.48), respectively (P = 0.019 for the 2nd day and P<0.001 for the other days). The levels of IL-6 in the cases were significantly different during the early stage of HFMD (2nd day, 3rd day), and the highest level occurred at 3rd day after disease onset, then significantly decreased from the 4th day (P<0.001). The levels of IL-6 among the 4 subgroups in the controls were not significantly different (P = 0.148). The levels of IL-10 among the cases were significantly higher than in the controls during the progression of HFMD from days 2 to 5 as follows: 16.86 (12.48∼27.45) vs. 10.18 (7.42∼16.70), 44.66 (41.33∼47.97) vs. 22.50 (19.77∼29.25), 77.00 (68.93∼82.14) vs. 34.64 (32.97∼39.00), and 57.20 (47.97∼62.42) vs. 35.65 (29.77∼42.99), respectively (P = 0.001 for the 2nd day and P<0.001 for the other days). The levels of IL-10 in the cases were significantly different and increased during the early stage of HFMD from the 2nd day to the 4th day and were the highest at the 4th day, then significantly decreased on the 5th day (P<0.001). The levels of IL-10 in the controls were significantly different from the 2nd day to 5th day (P<0.001).
(A, IL-4; B, IL-6; C, IL-10; D, IL-17; E, TNF-α; F, IFN-γ). The blue box represents cases and the green box represents controls.
The serum levels of IL-17 of the cases were not significantly different than the controls for the 4 stages and were 16.86 (12.48∼27.45) vs. 12.47 (5.93∼88.29), 15.54 (9.85∼31.87) vs. 36.32 (9.41∼71.86), 29.21 (10.07∼99.70) vs. 18.62 (8.54∼34.56), and 15.98 (9.85∼48.86) vs. 14.45 (8.43∼52.80), respectively (P = 0.894, 0.222, 0.338 and 0.613, respectively). In the cases, the levels of IL-17 increased from the 3rd day to the 4th day, and then decreased, although the results were not significantly different (P = 0.398). In the controls, the levels of IL-17 increased from the 2nd day to the 3rd day and then decreased; however the difference was not significant (P = 0.915).
The levels of TNF-α in the cases were significantly higher than in the controls during the four stages and were 63.03 (53.56∼87.42) vs. 19.42 (17.35∼22.90), 35.52 (25.43∼42.55) vs. 14.37 (10.08∼18.21), 26.98 (20.53∼31.86) vs. 9.06 (6.27∼16.52), and 29.60 (28.02∼33.34) vs. 6.15 (4.02∼11.46), respectively (P = 0.003 for the 3rd day and P<0.001 for the other days). The highest level of TNF-α in the cases occurred at the 2nd day after disease onset, and then significantly decreased from the 2nd day to 4th day (P<0.001), and there was no significant difference between the 4th day and the 5th day (P = 0.116). The levels of TNF-α in the controls also significantly decreased from the 2nd day to 5th day (P<0.001). The levels of IFN-γ in the cases were significantly higher than in the controls during the 4 days and were 35.02 (34.13∼36.29) vs. 38.93 (35.93∼40.80), 63.83 (61.40∼65.21) vs. 44.63 (36.01∼47.69), 56.10 (54.18∼57.94) vs. 41.91 (39.12∼44.63), and 57.23 (56.22∼58.51) vs. 44.84 (44.36∼46.41), respectively (P = 0.017 for the 2nd days and P<0.001 for the other days). The levels of IFN-γ of the cases significantly increased during the early stage of HFMD from the 2nd day to the 3rd day and then significantly decreased (P<0.001). The levels of IFN-γ in the controls were similar (P = 0.008).
Discussion
It is necessary to predict the occurrence of severe or fatal HFMD and identify risk factors for mild HFMD because fatal cases develop rapidly and progress to sympathetic hyperactivity, pulmonary edema and/or pulmonary hemorrhage, and cardiopulmonary collapse [1], [14]–[16]. To prevent the development of severity and avert death though close monitoring and timely intervention, particularly for children younger than 3-years old, the Chinese government has recommended screening criterion for severity. However, different hosts of the same enterovirus, such as EV71, have different clinical symptoms and outcomes [17].
Numerous studies compared the clinical symptoms and manifestations between severe or fatal HFMD and mild HFMD to identify severe and critical cases of HFMD [10], [18]. Currently, we highlight several important signs for characterizing cases of HFMD as severe. Neurological symptoms occurred in all severe cases, including hypersomnia, myoclonic jerks, and/or vomiting, and/or leg trembling, and/or febrile seizures. Notably, myoclonic jerks (100% in cases and 0 in controls) presented during the early stage of onset of severe HFMD, which is easily identifiable and can be used as an early sign to predict central nervous system (CNS) involvement. Chong et al. reported that vomiting may be a signal indicating CNS involvement [19], whereas Yang et al. showed that leg trembling was associated with severe HFMD [13]. In our study, vomiting occurred in 23.1% of the severe cases and 5.4% of the mild HFMD, and only 12.3% of the severe cases exhibited leg trembling. In addition, the severe cases presented a high proportion of complications for brainstem encephalitis, neurogenic pulmonary edema and sepsis. These results may be attributed to the higher number of EV71 positive cases compared to the controls [13]. Previous studies indicated that EV71 is more likely to cause serious complications than other enteroviruses and usually leads to brainstem encephalitis, neurogenic pulmonary edema, and circulation failure [14]–[16]. We also found that EV71 positive status was a significant risk factor for severity. However, serious complications often presented in the late stage of severity and etiological examination usually requires special equipment and is time-consuming, making this application difficult for general medical practice or for every patient [20]. Therefore, key laboratory findings are more helpful, except for significant clinical manifestations. such as myoclonic jerks.
In our patient population, the degree of fever (>39°C), duration of fever (>3 days) and length of in-hospital stay (>5 d) were risk factors for severity. Heart rate variability, using a simplified 5-minute recording, is also useful for detecting changes of the autonomic nervous system and disease progression [21]. No specific laboratory markers were found for biochemical and EV71-specific humoral immunity, except for EV71 infection as an indicator of severity. The biochemical results may be relevant to the spectrum of EV71 clinical manifestations. EV71 infection patients with pulmonary edema had significantly higher median blood levels of glucose and WBC count than patients without pulmonary edema [22], and had higher total WBC counts, absolute bandform counts, absolute neutrophil counts and platelet levels than those with isolated brainstem encephalitis [23]. In our study, because there was only one individual with pulmonary edema, a further stratified analysis was not conducted.
Cellular rather than humoral immunity is correlated with the clinical outcome of EV71 [11]. In our present study, the serum levels of IL-4, IL-6, IL-10, TNF-α and IFN-γ in severe patients were significantly higher than in mild patients during the 2nd to 5th day after disease onset, which indicated that IL-4, IL-6, IL-10, TNF-α and IFN-γ may be involved in disease severity. Whether the median serum levels detected in this study are the best thresholds to identify different stages of HFMD and severity onset, requires additional studies. IL-6 >70 pg/ml was the best predictor of EV71 encephalitis with pulmonary edema [24]. However, the criteria should be different to predict different complications, such as CNS symptoms. Earlier studies indicated that increased TNF-α and IL-6 secretion was detected after EV infection [24], [25]. Studies suggested that the enhanced expression of IL-1, IL-6, IL-10, IL-13, IFN-γ and TNF-α is associated with life-threatening complications in severe HFMD cases [22]–[24], [26], [27]. A recent study has shown that IL-17 is involved in the pathological process of EV71 infection [28]. In our study participants, there was no difference between cases and controls during the stages of disease. Wei et al. showed that an increase of EV71 epitope-specific Th2 type response might portend a poor prognosis for some HFMD patients [29].
In this study, the changes of the serum levels of IL-4, IL-6, IL-10, TNF-α and IFN-γ in severe patients were different. The levels of IL-4, IL-10 and IFN-γ increased for the first three days and then decreased. High levels of IL-6 and TNF-α were detected in severe patients at disease onset, and then decreased with disease progression.
Our study was designed as a nested series case-control study. The patients were enrolled gradually in different series according to their course of disease when they visited the hospital as follows: 2nd day, 3rd day, 4th day, and 5th day after HFMD onset. The samples of exposure biomarkers (cytokines) were collected, and the patients were then allocated into the case group (severe cases) and control group (mild cases) according to the follow-up situations. Therefore, the cases and controls came from the same original population. The changes or trend of the exposure biomarkers during the different stages of disease were analyzed and compared between cases and controls. The study was population-based and the results were of high credibility. This study describes the natural changes of the serum levels of IL-4, IL-6, IL-10, TNF-α and IFN-γ during the stages of HFMD and it progression. Because of medical ethics, the samples were collected only upon the admission of each patient to the hospital. The cytokine profile before and after immunoglobulin treatment significantly decreased for some proinflammatory cytokines in patients with EV71 [23], [30], [31]. However, there are several limitations in this study. The subjects were only hospitalized HFMD children and non-community patients, and the results were also affected by the clinical complications, such as neurological symptoms, brainstem encephalitis, neurogenic pulmonary edema, and even death.
The IL-4, IL-6, IL-10, TNF-α and IFN-γ levels correlated with the progress of HFMD. The levels of IL-4, IL-6, IL-10 and IFN-γ during the progression to severe HFMD significantly increased from the 2nd day to 4th day and then decreased. The levels of TNF-α were high on the first and second day and then significantly decreased. The peak levels of TNF-α, IL-6 and IL-10 in the cases occurred on the 2nd, 3rd, and 4th day after onset of HFMD, respectively.
Acknowledgments
The authors thank Doctor Yuanfang Shen and Doctor Yunping Qiao, Zhengzhou Children's Hospital, for allowing testing of the patients. We also thank Anam Nadeem for proof reading this article.
Author Contributions
Conceived and designed the experiments: GCD HYY LBS. Performed the experiments: LBS WMS RGZ. Analyzed the data: HYY LBS. Contributed reagents/materials/analysis tools: XHW FW WDZ YLX QTF MLS. Wrote the paper: HYY GCD.
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