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  • Open Access

Characterization of a subgroup of non-type 2 asthma with cow’s milk hypersensitivity in young subjects

  • 1Email author,
  • 1,
  • 2,
  • 3,
  • 2 and
  • 1
Clinical and Translational Allergy20199:12

https://doi.org/10.1186/s13601-019-0250-2

  • Received: 5 December 2018
  • Accepted: 31 January 2019
  • Published:

Abstract

Background

Asthma with atopy is often characterized by type 2 inflammation but less progress has been made in defining non-type 2 asthma. We have previously identified a subgroup of young non-atopic asthmatics with perceived food hypersensitivity and poor asthma control.

Objective

Our aim was to further characterize this subgroup of non-type 2 asthmatics, including the use of a broad panel of inflammation-related proteins.

Methods

Sex- and age-matched subjects (10–35 years old) were divided into three groups with regard to history of asthma and atopy: non-atopic asthmatics with perceived cow’s milk hypersensitivity but with IgE antibodies < 0.35 kUA/L (NAA; n = 24), non-atopic controls with IgE < 0.35 kUA/L (NAC; n = 24), and atopic asthmatics with IgE ≥ 0.35 kUA/L (AA; n = 29). Serum or plasma were analysed using the multi-allergen tests Phadiatop and fx5 (ImmunoCAP), a multiplex immunoassay comprising 92 inflammation-related proteins (Proseek Inflammation), and an ELISA for human neutrophil lipocalin (S-HNL). Fraction of exhaled nitric oxide (FeNO), blood eosinophil (B-Eos) count, C-reactive protein (CRP), airway responsiveness to methacholine (PD20), and asthma-related quality of life (mAQLQ) were also measured.

Results

NAA had lower FeNO (p < 0.001) and B-Eos count (p < 0.001), but scored worse on mAQLQ (p = 0.045) compared with AA. NAA displayed higher levels of matrix metalloproteinase-1 (MMP-1) compared with both NAC (p = 0.011) and AA (p = 0.001), and lower PD20 compared with NAC (p < 0.001). In NAA, S-HNL correlated negatively with PD20 (rho = − 0.048, p < 0.05) and CRP correlated negatively with mAQLQ (rho = − 0.439, p < 0.05).

Conclusion

In a subgroup of non-atopic young asthmatics with perceived cow’s milk hypersensitivity we observed poor asthma-related quality of life, airway hyperresponsiveness, and clinically relevant non-type 2 inflammation. MMP-1 was elevated in this group, which deserves further studies.

Introduction

Asthma associated with elevated type 2 immune responses is termed type 2 asthma, and is often related to atopy, especially in young subjects [1]. It is well-known that elevated fraction of exhaled nitric oxide (FeNO) and blood eosinophil (B-Eos) count are clinically useful type 2 biomarkers in asthma, and their simultaneous elevation has shown independent and additive predictive value for asthma morbidity [2, 3]. We have recently reported the persistence of clinically relevant type 2 inflammatory signals in young asthmatics with IgE antibody concentrations below 0.35 kUA/L, and we have suggested a cut-off of 0.10 kUA/L for ruling out type 2 inflammation [4].

Less progress has been made in defining non-type 2 asthma and few biomarkers have been described for this endotype. This type of asthma primarily affects older subjects [5], although its presence has also been described among young subjects [6]. It is likely that non-type 2 asthma includes more than one endotype and proven treatment options are limited. For example, non-type 2 (non-eosinophilic) asthma is less responsive to corticosteroids [7] and implicates the activation of neutrophils [8].

We have recruited a large sample of young (10–35 years) patients with asthma, from both primary and secondary care: the MIDAS cohort [2, 9]. Within this cohort, we have identified a non-atopic subgroup with perceived food hypersensitivity that showed lower asthma-related quality of life and poorer asthma control compared with both atopic asthmatics and non-atopic asthmatics without reported food hypersensitivity [6]. These subjects were characterized by low FeNO, suggesting non-type 2 asthma.

True non-type 2 asthma in young subjects has scarcely been investigated. In this study, our aim was to explore a biomarker pattern that could help define inflammatory mechanisms in these subjects with non-atopic asthma and perceived food hypersensitivity.

Methods

Patients

The Minimally-Invasive Diagnostic procedures in allergy, Asthma, or food hypersensitivity Study (MIDAS) asthma cohort was recruited from primary and specialist care facilities in Uppsala, Sweden [9, 10]. This cohort comprises 411 subjects aged 10–35 years, and the present study was initially based on 405 subjects with complete datasets, including IgE measurements and asthma control scores. The inclusion criteria were physician-diagnosed asthma and daily treatment with an inhaled corticosteroid (ICS) and/or an oral leukotriene-receptor antagonist (LTRA) during at least three of the past twelve months. The cohort also included 118 age- and sex-matched non-asthmatic controls randomly chosen from the population registry.

Grouping based on presence of asthma and IgE sensitization

Three subgroups were formed from this cohort with regard to history of asthma, food hypersensitivity, and atopy. The first group consisted of all asthmatics with perceived cow’s milk hypersensitivity, but without clear IgE sensitization to aeroallergens and food allergens (< 0.35 kUA/L), denoted non-atopic asthmatics (NAA, n = 24). NAA were extracted from a slightly larger group of non-atopic asthmatics with a history of perceived food hypersensitivity (see below). The second group consisted of control subjects without asthma and without clear IgE antibody sensitization (< 0.35 kUA/L) to aeroallergens and food allergens (non-atopic controls, NAC, n = 24). The third group consisted of atopic asthmatics (AA) with an IgE antibody concentration to aeroallergens ≥ 0.35 kUA/L (n = 29). The subjects in the three groups were age- and sex-matched (Fig. 1).
Fig. 1
Fig. 1

Description of the included study groups as regards IgE sensitization and perceived food hypersensitivity. IgE concentrations in kUA/L

Perceived food hypersensitivity symptoms

Each subject was asked to report any history of hypersensitivity reactions to food (egg white, cod fish, milk, soybean, wheat, or peanut). Perceived symptoms were grouped based on the organ affected: the lower airways (asthma), the upper airways (rhinitis, conjunctivitis), the oral cavity (oral allergy syndrome), the skin (atopic dermatitis, urticaria, and angioedema), the gastrointestinal tract (GI) (nausea, vomiting, abdominal pain, diarrhoea), and anaphylaxis (including self-reported). Out of the 30 non-atopic subjects with asthma with perceived food hypersensitivity, 24 reported cow’s milk hypersensitivity, three subjects wheat hypersensitivity, two subjects peanut hypersensitivity, and one subject had perceived cod fish hypersensitivity. We focused on the 24 subjects (80%) who reported cow’s milk hypersensitivity (NAA), based on the long-standing clinical recognition of this particular phenotype by one of the co-authors (LN), and for the sake of homogeneity.

Blood measurements

The presence of IgE antibodies was examined using a mix of nine aeroallergens (birch, timothy grass, mugwort, Dermatophagoides pteronyssinus, Dermatophagoides farinae, Cladosporium herbarum, cat, dog, and horse; Phadiatop) and a mix of six food allergens (egg white, cod fish, milk, soybean, wheat, and peanut; fx5) [11]. Serum IgE antibodies, total IgE, IgG/IgA antibodies and eosinophilic cationic protein (S-ECP) were measured in the ImmunoCAP system (ImmunoDiagnostics, Thermo Fisher Scientific, Uppsala, Sweden). Subjects were considered to be atopic if they had IgE antibody concentrations ≥ 0.35 kUA/L.

Serum human neutrophil lipocalin (S-HNL) concentrations were measured in an ELISA (Diagnostics Development, Uppsala, Sweden). Plasma was analysed using a panel of 92 inflammation-related proteins (Proseek Multiplex Inflammation; Olink Bioscience, Uppsala, Sweden) [12]. The inflammation panel was based on a multiplex proximity extension immunoassay (PEA), enabling analysis of 92 proteins simultaneously. The data were given in the form of relative quantification and expressed as normalized protein expression (NPX). Further, plasma C-reactive protein (P-CRP) was analysed using an immunoturbidimetric method (CRP Vario, Abbott, Illinois, USA), and blood cells were counted using an automated cell counter (Cell-Dyn Sapphire, Abbott, Illinois, USA); both analyses were performed at Uppsala University Hospital.

Asthma symptoms, attacks and medication

The degree of asthma control was assessed using the Asthma Control Test (ACT) [13]. The total ACT score is between 5 and 25, with a lower score indicating poorer asthma control. A score ≥ 20 indicates well-controlled asthma. The mini asthma quality of life questionnaire (mAQLQ) consists of 15 questions. The score ranges from 1 to 7, with a lower score indicating a poorer quality of life [14]. Use of ICS and LTRA was recorded in the interviews. Asthma symptoms during the last 12 months were also recorded [15]. Subjects were divided into groups based on whether or not they had had a recent asthma attack (last three months, self-reported).

Exhaled nitric oxide

The fraction of exhaled nitric oxide (FeNO) was measured in accordance with the American Thoracic Society (ATS)/European Respiratory Society recommendations [16] using a chemiluminescence analyser at an exhalation flow rate of 50 mL/s (NIOX Flex; Aerocrine AB, Solna, Sweden). The mean value from three exhalations (or two, if the first two NO measurements were within 10% of each other) was used for statistical analysis.

Lung function

Forced expiratory volume in one second (FEV1) was measured using a Masterscope spirometer (Viasys Healthcare GmbH, Höchberg, Germany). Recommendations from the ATS were followed [17]. The subjects were subdivided into groups with reduced or normal lung function (FEV1 < 80% or ≥ 80%). The percent of predicted values for FEV1 were calculated on the basis of Hedenström reference values for those ≥ 18 years of age [18, 19] and Solymar reference values for subjects < 18 years of age [20]. A bronchial provocation test was performed with Aerosol Provocation System (Viasys Healthcare GmbH, Höchberg, Germany) using a single concentration of methacholine and increasing doses up to a maximal cumulative dose of 3.63 mg methacholine. Airway responsiveness was defined as normal if the cumulative dose causing a reduction in FEV1 of 20% (PD20) was > 1.0 mg, borderline-to-mild at 0.3–1.0 mg, and moderate-to-severe at < 0.3 mg, in accordance with Schulze et al. [21].

Statistics

All statistical analyses were performed using STATA/IC 13.1 (StataCorp LP, College Station, Texas, USA). If continuous variables had a distribution skewed to the right, a geometric mean with a 95% confidence interval was used for descriptive statistics and Mann–Whitney U test (for continuous variables) and Fisher’s exact test (for categorical variables) were used for group comparisons. Seven subjects with fx5 between 0.10 and 0.34 kUA/L and three subjects with Phadiatop between 0.10 and 0.34 kUA/L were found in the NAA group, while the remaining 14 had both Phadiatop and fx5 below 0.10 kUA/L. We generated a subgroup based on detectable IgE levels between 0.10 and 0.34 kUA/L and compared it to the rest of the NAA group.

Multivariate ANOVA with concomitant adjustment for confounders: age, gender, body mass index (BMI), and smoking was used in group comparisons for candidate proteins, and the robustness of the test was evaluated using bootstrapping. The p values were adjusted for multiple testing using the Benjamin-Hochberg procedure. This procedure is based on controlling the false discovery rate and limiting that to a predefined value (0.05) [22]. We performed exploratory correlation analyses between the different biomarkers, including the significant inflammation-related proteins, and clinical outcomes (mAQLQ, ACT, PD20, recent asthma attacks) in each group, using the Spearman’s test. A p value < 0.05 was considered statistically significant and p < 0.10 indicated a trend.

Results

Subject characteristics

NAA had increased airway responsiveness to methacholine, reduced FEV1/FVC ratio, and were shorter than NAC (Table 1). Further, NAA had lower levels of type 2 biomarkers, but scored worse on mAQLQ compared with AA. No differences in blood total leukocyte, monocyte, lymphocyte, or basophil counts were noted between the groups (data not shown). Asthma medication use, lung function, airway responsiveness, and asthma symptoms were similar in NAA and AA. The clinical and inflammatory outcomes were not significantly different between the subgroup of NAA with detectable IgE levels (0.10–0.34 kUA/L) and the rest of the NAA group (data not shown). Cow’s milk-induced symptoms from the GI tract were present among all NAA, but only in 10% (n = 3) of the AA group (Additional file 1: Table E1). NAA did not report any anaphylaxis or symptoms from the upper airways and oral cavity, but had higher prevalence of milk-induced other symptoms compared with AA. NAA had lower total IgG antibody concentrations to α-lactalbumin and β-lactoglobulin, and lower IgG4 to α-lactalbumin than AA (Table 2). Furthermore, NAA had lower IgA antibody concentration and a trend for lower IgG to casein than NAC. In the larger group with non-atopic asthma (n = 82, see Fig. 1), subjects with any perceived food symptoms (n = 30) scored worse on ACT and mAQLQ when compared to subjects without food symptoms, whereas no other differences in the studied inflammatory or clinical outcomes were observed between these two groups (Additional file 1: Table E2).
Table 1

Characterization of the three groups included in the study. Comparison of the non-atopic asthmatics (NAA) to non-atopic controls (NAC) and atopic asthmatics (AA)

 

NAA (n = 24)

NAC (n = 24)

AA (n = 29)

p value NAA-NAC

p value NAA-AA

Females (%)

60

54.1

48.2

0.687

0.398

Age (years)

18.5 ± 5.90

19.5 ± 5.98

18.4 ± 5.80

0.526

0.946

Height (cm)

163 ± 13.6

172 ± 11.5

166 ± 14.3

0.021

0.553

Weight (kg)

59.3 ± 15.9

65.9 ± 16.2

61.6 ± 19.3

0.161

0.646

FeNO (ppb)

9.78 (8.15, 11.7)

10.5 (9.01, 12.3)

29.2 (19.4, 44.2)

0.534

< .001

B-Eos

0.118 (0.088, 0.159)

0.086 (0.067, 0.110)

0.357 (0.257, 0.498)

0.097

< .001

B-Neu

3.23 (2.68, 3.90)

3.13 (2.65, 3.70)

3.26 (2.85, 3.72)

0.796

0.941

Phadiatop

0.053 (0.041, 0.069)

0.046 (0.037, 0.057)

22.8 (12.5, 41.6)

0.349

< .001

fx5

0.054 (0.038, 0.073)

0.053 (0.038, 0.073)

2.77 (0.963, 7.98)

0.627

< .001

Total IgE

22.8 (14.1, 36.6)

15.6 (8.81, 27.7)

458 (334, 628)

0.300

< .001

S-ECP

9.76 (7.62, 12.5)

8.33 (6.02, 11.5)

20.0 (14.9, 26.9)

0.423

< .001

P-CRP

0.510 (0.267,0.973)

0.522 (0.288, 0.945)

0.551 (0.327, 0.928)

0.956

0.846

S-HNL

75.2 (63.0, 89.7)

73.4 (62.7, 86.0)

72.1 (63.6, 81.8)

0.835

0.684

Smoking (%)

0

8.33

6.89

0.146

0.187

ICS (µg)

438 (312, 615)

395 (307, 509)

0.876

LTRA (%)

24.0

20.7

0.999

ACT

18.8 ± 4.51

20.0 ± 2.89

0.140

mAQLQ

5.17 ± 1.20

5.74 ± 0.821

0.045

FEV1 (%)

92.7 ± 12.5

98.0 ± 13.5

91.1 ± 16.3

0.156

0.701

FEV1 < 80 (%)

16.0

4.17

24.1

0.178

0.468

FEV1/FVC

82.6 (79.5, 85.8)

87.7 (85.4, 90.1)

80.5 (76.8, 84.2)

0.011

0.402

PD20 (mg)

0.677 (0.297, 1.54)

4.56 (3.25, 6.41)

0.393 (0.130, 1.19)

< .001

0.422

Recent asthma attacks

56.0

48.2

0.320

Mean ± SD, Geometric mean (95% CI). IgE concentrations in kUA/L, white blood cells in × 109/L, P-CRP in mg/L, and S-ECP and S-HNL in µg/L

Table 2

IgG and IgA antibody concentrations (mg/L) in the included study groups. Comparisons of non-atopic asthmatics (NAA) with non-atopic controls (NAC) and atopic asthmatics (AA)

 

NAA (n = 24)

NAC (n = 24)

AA (n = 29)

p value NAA-NAC

p value NAA-AA

IgG α-LA

1.11 (0.724, 1.72)

1.46 (0.942, 2.27)

3.87 (2.26, 6.63)

0.379

0.001

IgG β-LG

2.43 (1.42, 4.14)

2.50 (1.38, 4.52)

7.31 (4.24, 12.6)

0.975

0.017

IgG casein

7.07 (5.07, 9.86)

10.3 (7.24, 14.7)

9.97 (7.43, 13.3)

0.085

0.078

IgG4 α-LA

0.200 (0.086, 0.461)

0.123 (0.047, 0.318)

0.975 (0.405, 2.34)

0.968

0.002

IgG4 β-LG

0.805 (0.330, 1.96)

0.499 (0.186, 1.33)

2.77 (1.47, 5.22)

0.529

0.052

IgG4 casein

1.20 (0.698, 2.08)

1.18 (0.669, 2.09)

1.55 (0.974, 2.48)

0.826

0.497

IgA α-LA

0.520 (0.479, 0.565)

0.500 (0.500, 0.500)

0.522 (0.477, 0.570)

0.327

0.936

IgA β-LG

0.520 (0.479, 0.564)

0.540 (0.483, 0.603)

0.566 (0.500, 0.641)

0.531

0.234

IgA casein

0.819 (0.581, 1.15)

1.37 (0.978, 1.94)

0.921 (0.681, 1.24)

0.014

0.471

α-LA = α-lactalbumin, β-LG = β-lactoglobulin. Geometric mean (95% CI)

Exploratory proteomic analysis and correlation between inflammatory markers

For 79 out of 92 proteins (86%) in the Proseek panel, at least 50% of the observations were above the detection limit, and these were included in further analyses (see Additional file 1: Table E3). Three proteins showed significant group differences in an ANOVA adjusted for confounders (crude p value < 0.05): MMP-1, FGF5, and IL-10. After correction for multiple testing, MMP-1 was the only protein that maintained a trend (p = 0.10). Based on this, we performed correlation analyses between MMP-1 and all other inflammation markers in the NAA group: MMP-1 correlated significantly with FeNO, CRP, IL-8, IL-20, and CXCL9 (Table 3). When repeating the correlation analysis for these proteins in AA and NAC, MMP-1 was found to correlate with CRP and IL-20 in AA and with CRP in NAC. IL-6 correlated with CRP in NAA (rho = 0.422, p = 0.035), but IL-6 did not correlate with MMP-1 in this group (rho = 0.055, p = 0.792). Furthermore, in NAA, CXCL9 correlated significantly with FeNO (Additional file 1: Table E4). MMP-1 was higher in NAA compared with both NAC and AA (Fig. 2), and IL-8 was found to be higher in NAA than in NAC, whereas CXCL9 was significantly lower in NAA than AA (Table 4).
Table 3

Correlations (rho) between MMP-1 and different inflammatory markers in the included study groups

MMP-1

FeNO

CRP

IL-8

IL-20

CXCL9

NAA

0.509*

0.478*

0.553*

0.407*

0.457*

NAC

− 0.337

0.541*

0.077

− 0.066

0.095

AA

− 0.035

0.465*

0.314(*)

0.387*

0.045

*p < 0.05, (*)p < 0.10

Fig. 2
Fig. 2

Plasma levels of MMP-1 in the included study groups. Geometric mean (95% CI)

Table 4

Group comparisons for the proteins significantly correlating with MMP-1 (concentrations in NPX)

 

NAA (n = 24)

NAC (n = 24)

AA (n = 29)

p value NAA-NAC

p value NAA-AA

IL-8

5.13 (4.98, 5.28)

4.84 (4.65, 5.04)

5.00 (4.87, 5.13)

0.032

0.160

IL-20

0.255 (0.180, 0.363)

0.262 (0.182, 0.378)

0.259 (0.185, 0.363)

0.706

0.739

CXCL9

5.64 (5.41, 5.87)

5.72 (5.51, 5.94)

6.03 (5.78, 6.30)

0.660

0.039

Geometric mean (95% CI)

Correlations between potential biomarkers and clinical outcomes

In NAA, S-HNL correlated negatively with PD20 (Table 5). Furthermore, significant negative correlations were noted between CRP, and ACT and mAQLQ scores, respectively. There were also trends for significant negative correlations between the ACT score, and MMP-1 and IL-8, respectively, as well as between mAQLQ and B-Neu. No associations between type 2 biomarkers and clinical outcomes were found in the NAA group. In AA, the type 2 biomarkers FeNO, B-Eos, and S-ECP all correlated negatively with PD20, and total IgE correlated negatively with FEV1 (Table 6). MMP-1 showed a weak but significant negative correlation with ACT score, whereas CRP correlated positively with PD20, and B-Neu showed a similar trend in this group.
Table 5

Correlations (rho) between clinical outcomes and inflammatory markers in NAA

NAA

ACT

mAQLQ

PD20

FEV1

FEV1/FVC

P-CRP

− 0.402*

− 0.439*

− 0.299

− 0.294

− 0.043

S-HNL

0.144

− 0.030

− 0.048*

0.243

0.238

B-Neu

− 0.323

− 0.387(*)

− 0.126

0.042

0.138

B-Eos

0.268

0.003

− 0.333

0.192

− 0.095

S-ECP

0.030*

0.175

− 0.332

0.294

0.078

Total IgE

0.008

0.216

0.075

0.420

0.189

MMP-1

− 0.359(*)

− 0.320

− 0.030

− 0.020

0.255

IL-8

− 0.358(*)

− 0.266

0.079

− 0.122

− 0.152

IL-20

− 0.131

− 0.089

0.336

− 0.047

0.525

CXCL9

0.059

− 0.054

− 0.183

0.009

− 0.151

FeNO

− 0.081

− 0.003

− 0.152

0.072

− 0.108

*p < 0.05, ** p < 0.01, (*)p < 0.10

Table 6

Correlations (rho) between clinical outcomes and inflammatory biomarkers in AA

AA

ACT

mAQLQ

PD20

FEV1

FEV1/FVC

P-CRP

− 0.089

− 0.018

0.421*

0.142

− 0.038

S-HNL

− 0.075

− 0.142

0.213

0.226

− 0.134

B-Neu

− 0.051

0.100

0.365(*)

0.163

0.096

B-Eos

− 0.217

− 0.103

− 0.788**

− 0.186

− 0.213

S-ECP

− 0.083

− 0.219

− 0.662**

− 0.163

− 0.157

Total IgE

− 0.046

0.357

− 0.134

− 0.651*

0.236

MMP-1

− 0.038*

− 0.225

0.184

0.162

− 0.100

IL-8

− 0.207

0.150

− 0.064

− 0.068

0.015

IL-20

− 0.116

− 0.233

0.057

0.158

0.139

CXCL9

0.128

0.435

− 0.343

0.006

− 0.165

FeNO

− 0.049

− 0.011

− 0.725**

− 0.052

− 0.291

*p < 0.05, **p < 0.01, (*)p < 0.10

Discussion

The main finding of this study was that in non-atopic asthmatics with perceived cow’s milk hypersensitivity, despite being free from type 2 inflammation, we observed airway hyper-responsiveness, reduced FEV1/FVC ratio, and lower asthma-related quality of life than in those with atopic asthma. Furthermore, in this group, airway responsiveness, asthma control, and asthma-related quality of life all associated with signs of non-type 2 inflammation, such as blood neutrophil count, CRP, HNL, IL-8, and MMP-1. MMP-1 was the biomarker best distinguishing this group of non-atopic asthmatics from both controls and atopic asthmatics.

In non-atopic asthmatics reporting hypersensitivity reactions to cow’s milk, correlations between type 2 biomarkers and clinical outcomes were absent. Instead, correlations were observed between HNL and methacholine responsiveness, and between CRP and both mAQLQ and ACT; such correlations were absent in the atopic group, indicating an immunological background distinct from the type 2 spectrum. HNL and CRP have mainly been used as diagnostic tools for distinguishing bacterial from viral infections [23, 24]. However, a few studies have associated HNL and CRP to airway inflammation and to the prediction of asthma status [2527], but these markers seem to be resistant to corticosteroid treatment [28]. Several studies have emphasized the role of neutrophilic inflammation in corticosteroid-resistant asthma involving IL-8 as a potent mediator [2931]. Since corticosteroids may even promote neutrophil survival [32], attempts targeting neutrophilic inflammation have been made, but with only minor clinical effects, and validated biomarkers are lacking at the moment [1, 33]. Our results revealed airway hyper-responsiveness and systemic inflammation in non-atopic subjects with ongoing asthma medication, indicating the need for new therapeutic strategies.

In contrast, the atopic asthmatics showed higher levels of all type 2 biomarkers (FeNO, B-Eos, S-ECP, and IgE) than non-atopic asthmatics. Furthermore, the degree of type 2 inflammation correlated with clinical outcomes. For example, FeNO, B-Eos, and S-ECP correlated with methacholine responsiveness. Interestingly, MMP-1 was found to correlate negatively with ACT score, but not with type 2 biomarkers, in this group of atopic asthmatics. Furthermore, CRP and blood neutrophil count associated positively with methacholine reactivity, indicating a down-regulation of innate mechanisms by type 2 inflammation.

Studies have suggested that some biomarkers are implicated in both type 2 and non-type 2 inflammatory pathways, making the distinction more complicated. For example, matrix metalloproteinases (MMPs) are endopeptidases that are involved in the pathophysiology of airway inflammation in allergic asthma, but they may also be involved in monocyte recruitment to inflammatory sites [34, 35]. Furthermore, MMPs has been implicated in the pathophysiology of intestinal inflammation by promoting neutrophil recruitment in the intestinal wall and activating T cells, leading to gastrointestinal damage [36]. Interestingly, it was recently shown that plasma MMP-1 was reduced after the introduction of exclusive enteral nutrition in patients with juvenile idiopathic arthritis, another disease where the involvement of the GI tract has been suggested [37]. A novel finding of the present study was that MMP-1 was the biomarker most significantly elevated in non-atopic subjects as compared with in either atopic asthmatics or non-atopic controls. According to other studies, MMP-1 expression is believed to be stimulated by type 2 cytokines and thereby contributes to airway hyper-responsiveness in allergen-induced asthma [38, 39]. Moreover, the possible activation of MMP-1 by mast cell tryptase could result in airway hyper-responsiveness and airway narrowing [40]. Interestingly, in the non-atopic asthma group, FeNO, MMP-1, and CXCL9 all inter-correlated, whereas this was not seen in atopic asthmatics. CXCL9, a chemoattractant for T lymphocytes, involving elements of mixed type 2 and non-type 2 bronchial inflammation in asthma, is upregulated by IFN-γ, a Th1 cytokine [4143]. In addition, it has previously been suggested that basal NO formation in the respiratory epithelium is dependent on homeostatic IFN-γ [44]. However, an IFN-γ-mediated basal regulation of airway NO formation may not be easily detected in atopic asthmatics, where IL-4/IL-13-driven NO formation will dominate [44]. Thus, we suggest that the association between FeNO and plasma CXCL9, and possibly MMP-1, depends on the expression of IFN-γ. No significant correlations between these biomarkers and IFN-γ were noted in this study, but this could be due to many observations being below the detection limit for IFN-γ (close to 50%). Furthermore, we could show that MMP-1 correlated with CRP, but not IL-6, in non-atopic asthmatics, whereas IL-6 and CRP correlated with each other as expected [45]. This may indicate that the association between MMP-1 and CRP relies on IL-1β and/or tumour necrosis factor (TNF), both of which are also involved in CRP induction. However, this could not be confirmed in the present study since IL-1β was not part of the Proseek panel, and TNF was below the detection limit in more than 50% of the observations. However, as a support to this hypothesis, IL-20, which is known to be induced by IL-1β and TNF [46], correlated with MMP-1 in non-atopic asthmatics in the present study. IL-20 has also been suggested to be involved in airway remodelling in asthma [47]. The fact that MMP-1 correlated with quite diverse inflammation markers including FeNO, IL-8, CRP etc., implicates multiple cellular origin of this proteinase.

An interesting feature in the non-atopic group with perceived milk hypersensitivity was the poorer asthma-related quality of life as compared with the atopic asthma group. We have previously published this in non-atopic subjects reporting any food hypersensitivity [6], and could now confirm this finding in the more homogenous subgroup specifically reporting milk hypersensitivity. The present results further strengthen the earlier observations, since we managed to objectively confirm the presence of airway disease including airway hyper-responsiveness and reduced FEV1/FVC ratio. We have recently reported data showing weak type 2 inflammatory signals in young asthmatics with IgE antibody concentrations below 0.35 kUA/L, suggesting a cut-off of 0.10 kUA/L for ruling out the presence of such inflammation [4]. In the present study, 58% of the subjects that reported hypersensitivity to cow’s milk had undetectable IgE antibody concentrations (< 0.10 kUA/L). When the subgroup with detectable IgE (0.10–0.34 kUA/L) was compared with the subjects with undetectable IgE, no differences in clinical or inflammatory indices were noted. We assume that the distribution of IgE levels in this particular group of asthmatics is similar to that in the normal population, but that the low IgE antibody concentrations do not reflect mechanisms driving the asthma disease, just as they do not in healthy controls.

Non-IgE-mediated cow’s milk hypersensitivity characterized the studied group. We also examined IgG and IgA antibodies against different cow’s milk proteins, but no elevated levels were found in the non-atopic asthmatics. Instead, lower antibody levels against casein were seen than in controls, which could be the consequence of lower consumption of milk due to the perceived symptoms.

A strength of the present study was the recruitment of young asthmatics from both primary and secondary care units. Three approximately equal-sized subgroups that were age- and sex-matched were created and both non-atopic healthy controls and atopic asthmatics were used for comparisons. However, this could also be considered a limitation due to the relatively small number of subjects in each group, even though the subjects that were hypersensitive to cow’s milk were taken from a large sample of asthmatics (n = 408). Another limitation of this study may be that the cow’s milk hypersensitivity was self-reported and not confirmed in provocation tests. One should be aware of the similarity of the symptoms between non-IgE-mediated cow’s milk hypersensitivity and other gastrointestinal disturbances, such as lactose intolerance, gastrointestinal infections, or irritable bowel syndrome. However, very few subjects reported gastrointestinal disorders other than perceived food hypersensitivity in the interviews.

In conclusion, we found that non-atopic subjects with cow’s milk hypersensitivity constituted almost 6% of a representative sample of young asthmatics. These asthmatics were characterized by airway hyper-responsiveness, reduced lung function, and poor asthma-related quality of life. Biomarkers, including those not extensively investigated previously, showed clear signs of clinically relevant non-type 2 inflammation. Future studies may help us understand how these biomarkers might direct towards more appropriate treatment of young subjects with non-atopic asthma.

Abbreviations

AA: 

atopic asthmatics

ACT: 

Asthma Control Test

ATS: 

American Thoracic Society

B-Eos: 

blood eosinophil

B-Neu: 

blood neutrophil

CXCL: 

C-X-C motif chemokine ligand

FeNO: 

fraction of exhaled nitric oxide

FEV1

forced expiratory volume in 1 s

FGF: 

fibroblast growth factor

ICS: 

inhaled corticosteroid

IFN-γ: 

interferon gamma

IgE: 

immunoglobulin E

IL: 

interleukin

α-LA: 

α-lactalbumin

β-LG: 

β-lactoglobulin

LTRA: 

leukotriene-receptor antagonist

mAQLQ: 

mini Asthma Quality of Life Questionnaire

MMP: 

matrix metalloproteinase

NAA: 

non-atopic asthmatics

NAC: 

non-atopic controls

NPX: 

normalized protein expression

PD20

provocative dose causing a fall in FEV1 by 20%

PEA: 

Proximity Extension Assay

P-CRP: 

plasma C-reactive protein

ppb: 

parts per billion

S-ECP: 

serum eosinophilic cationic protein

S-HNL: 

serum human neutrophil lipocalin

Th: 

T helper

Declarations

Author’s contributions

NT in cooperation with AM have performed the data analysis. NT wrote the manuscript. KA, LN and AM have designed the study and developed the methodology. All the authors read and approved the final version of the manuscript.

Acknowledgements

We thank Emil Nilsson, data scientist for his valuable contribution in the proteomics analysis.

Competing interests

Niclas Rydell is an employee of Thermo Fisher Scientific, and Kjell Alving has received research material from the same company.

Availability of data and materials

Not applicable.

Consent for publication

Not applicable.

Ethics approval and consent to participate

The Uppsala Regional Ethical Review Board approved the study (Registration Number 2009/349) and all subjects and their legal guardians, when appropriate, gave written informed consent.

Funding

The MIDAS study was performed within an industry-academy collaborationframework initiated by the Swedish Government Agency for Innovation Systems (VINNOVA, SAMBIO program), where Aerocrine AB (producer of exhaled NO devices) and Thermo Fisher Scientific, ImmunoDiagnostics (producer of allergy tests) were partners and co-financed the program. Further funding was received from Gillberg’s Foundation, Bror Hjerpstedt’s Foundation, Hesselman’s Foundation, the Swedish Foundation for Strategic Research, the Swedish Heart and Lung Foundation, and the Swedish Asthma and Allergy Association’s Research Foundation.

Publisher’s Note

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Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Women’s and Children’s Health, Uppsala University Hospital, Uppsala University, 751 85 Uppsala, Sweden
(2)
Department of Medical Sciences, Clinical Physiology, Uppsala University, Uppsala, Sweden
(3)
Thermo Fisher Scientific, ImmunoDiagnostics, Uppsala, Sweden

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