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Chemokines during anaphylaxis: the importance of CCL2 and CCL2-dependent chemotactic activity for basophils

Abstract

Background

The role of chemokines in anaphylaxis is unclear.

Methods

We prospectively recruited 49 patients presenting to the emergency department with an acute episode of anaphylaxis and 28 healthy subjects. We measured serum levels of the chemokines CCL2, CCL5, CCL7, CCL8, CCL11, CCL13, CCL17, CCL21, CCL22, CCL24, and CCL26, tryptase, the absolute number of circulating basophils, monocytes, lymphocytes, and PMNs, and whole blood FCER1A, CPA3 and HDC gene expression at two time points: during the anaphylactic episode and in convalescent samples collected approximately 3 months later. We then investigated the in vitro chemotactic activity of chemokines induced during anaphylaxis for the in vitro migration of the corresponding cells.

Results

Only CCL2 chemokine levels were significantly increased in anaphylaxis samples (median 514 pg/ml) compared to convalescent samples (284 pg/ml, P < 0.0001) and healthy subjects (279 pg/ml, P < 0.0001); there was no significant difference in any of the other chemokines. There was a significant positive correlation between the rates of increase of serum CCL2 (median [range]: 106.0% [− 44.7% to 557.4%]) and tryptase (133.8% [− 6.6% to 893.4%]; r = 0.68, P < 0.0001) and between the acute concentration of serum CCL2 and the acute concentration of serum tryptase (r = 0.77, P < 0.0001). The number of circulating basophils, but not other blood cells, significantly decreased during anaphylaxis (median 5.0 vs. 19.1 cells/µl in convalescent samples; P < 0.0001); a decrease in whole-blood gene expression of basophil markers (P ≤ 0.0018) confirmed these changes. Anaphylactic serum enhances the in vitro migration of basophils via CCL2-dependent chemotactic activity; in contrast, no CCL2-dependent chemotactic activity was observed for convalescent samples.

Conclusions

Our findings imply an important and specific role for CCL2-mediated chemotactic activity in the pathophysiology of human anaphylaxis.

Background

Anaphylaxis is a potentially life-threatening, rapidly progressing systemic hypersensitivity reaction, often following exposure to a small amount of allergen, including insect venom, foods, and medications [1]. The major immunopathogenesis and pathophysiological mechanisms of anaphylaxis involve IgE antibodies, effector mast cells, basophils and the mediators histamine, platelet-activating factor, and cysteinyl leukotrienes [2,3,4]. However, anaphylaxis also induces changes in other mediators, including tryptase [5,6,7], prostaglandins [8], cytokines [6, 9], and chemokines [7]. A recent study demonstrated an increase in CCL2 (C-C Motif Chemokine Ligand 2) levels during human anaphylaxis [7], with no changes demonstrated for the chemokines CCL5 [7] and CCL11 [6, 7]. The chemokines CCL2, CCL5, and CCL11 are involved in basophil migration, with the CCR2 ligand CCL2 and the CCR3 ligand CCL11 eliciting the most potent migratory responses [10]. Chemokines that diffuse out from the site of release and form a concentration gradient to which leukocytes respond and migrate might be involved in the recruitment of basophils [4] or other potential effector cells of anaphylaxis, including monocytes/macrophages [11], neutrophils [12, 13], and platelets [14], to the inflamed tissue sites.

In addition to CCL2 [7], several other chemokines might be involved in different allergic diseases. For monocyte chemoattractant proteins (MCPs), an increase in CCL7 levels in allergic conjunctivitis [15], an increase in CCL8 levels in chronic/eosinophilic atopic dermatitis [16], and an increase in CCL13 levels in allergic rhinitis [17] were demonstrated. For eotaxin chemokines, CCL11 and CCL24 levels were increased in asthma and allergic rhinitis [18], and CCL26 levels were increased in allergic rhinitis [17] and atopic skin inflammation [19]. CCL5, CCL17, CCL21, and CCL22 were also reported to be involved in asthma, atopic dermatitis, allergic rhinitis and drug hypersensitivity syndrome [20,21,22,23,24,25].

Given that different chemokines might be important in allergic diseases, we performed a series of interlinked studies to better understand the role of chemokines and their chemotactic activity in anaphylaxis. In a prospective study during and after anaphylaxis caused by Hymenoptera venom, medication, food, or other (idiopathic), we investigated the serum concentration of a large panel of different chemokines (CCL2, CCL5, CCL7, CCL8, CCL11, CCL13, CCL17, CCL21, CCL22, CCL24, and CCL26), which were previously described in allergic diseases [6, 7, 15,16,17,18,19,20,21,22,23,24,25]. In whole blood samples, we measured the absolute numbers of circulating basophils, monocytes, lymphocytes, and polymorphonuclear leukocytes (PMNs) and the gene expression of the basophil markers FCER1A, carboxypeptidase A3 (CPA3) and L-histidine decarboxylase (HDC). We then proceeded to analyse the chemotactic activity of chemokines that are induced during anaphylaxis in the controlled setting of a cellular in vitro migration assay.

Methods

Study participants

We prospectively recruited 49 patients (24 females; age, 19–82 years; Table 1) presenting to the Emergency Department of University Hospital Golnik, Slovenia, with an acute episode of anaphylaxis (January 2017 to October 2019). The reaction was caused by an insect sting in 26 patients, by medication in 14 patients, by food in 5 patients and by other triggers in 4 patients (idiopathic in 2 patients and infection in 2 patients); 21 experienced Mueller [26] grade IV, 16 experienced grade III, 6 experienced grade II, and 6 experienced grade I reactions (Table 1). We collected blood samples during the reaction (at presentation to the emergency department; in all patients we routinely measured acute serum tryptase, Table 1) and convalescent samples after the anaphylactic episode. None of those patients were included in our previous study of anaphylaxis [7]. The median time from the onset of symptoms to sample collection was 100 min (range 30 to 240 min); convalescent samples were collected a median of 80 days after the anaphylactic episode (Table 1). In 30 patients, we measured serum chemokines and tryptase, and in 26 patients, we measured blood absolute cell counts and gene expression (of those 41 patients, 15 were in both subgroups); for comparison, we recruited 20 healthy subjects (13 females; age, 20–76 years) (Additional file 1: Table S1). The serum of 8 anaphylactic patients and isolated basophils of 8 healthy subjects (4 females; age, 25–44 years) were used for in vitro migration experiments (Additional file 1: Table S1).

Table 1 Characteristics of the patients

Ethical approval was obtained from the Slovenian National Medical Ethics Committee. All subjects provided written informed consent.

Serum chemokines and tryptase, absolute cell counts, and gene expression

We measured serum concentrations of the MCP chemokines CCL2/MCP-1, CCL7/MCP-3, CCL8/MCP-2, and CCL13/MCP-4; the eotaxin chemokines CCL11/Eotaxin, CCL24/Eotaxin-2 and CCL26/Eotaxin-3; and the chemokines CCL5/Rantes, CCL17/TARC, CCL21/SLC and CCL22/MDC using ELISAs according to the manufacturers’ instructions (Quantikine R&D Systems, Minneapolis, MN, USA; Abnova, Taipei, Taiwan; and Biolegend, San Diego, California, CA, USA). We measured serum tryptase (ImmunoCAP, Thermo Fisher, Uppsala, Sweden), and concentrations that exceeded 11.4 µg/l were considered increased. Enumeration of circulating basophils (CD123+HLA-DR− cells), monocytes, lymphocytes, and PMNs in fresh whole blood was performed via flow cytometry as previously described [7, 27]. FCER1A, CPA3, and HDC gene expression was analysed in whole blood samples (PAXgene, PreAnalytiX, Hombrechtikon, Switzerland) as previously described [7, 27]. Detailed methods are provided in Additional file 1.

Cell separation and in vitro migration assays

CCR2 surface expression on basophils of healthy donors was determined by anti-CCR2 mAb (CD192; Miltenyi Biotec, Bergisch Gladbach, Germany) staining, and basophils were isolated from peripheral whole blood by negative immunomagnetic selection (Miltenyi Biotec, Bergisch Gladbach, Germany) and exactly quantified by absolute flow cytometry basophil counts as previously described (CD123+HLA-DR− cells and microbeads) [7, 27]. For the migration assay, we used modified Boyden chamber and polycarbonate membrane cell culture inserts (Corning Inc., New York, USA). A total of 20,000 basophils were added to the upper wells, and the samples to be tested were placed in the lower wells. After incubation for 30 to 150 min at 37 °C, we collected the cells that had migrated to the lower wells and quantified them by absolute basophil counts [7, 27]. Basophil migration was calculated by using the following equation:

$$ {\text{Basophil}}\;{\text{migration}}\left( \% \right) = \left( {{\text{absolute}}\;{\text{number}}\;{\text{of}}\;{\text{migrated}}\;{\text{basophils}}/{\text{absolute}}\;{\text{number}}\;{\text{of}}\;{\text{seeded}}\;{\text{basophils}}} \right) \times 100. $$

For control experiments, we used recombinant CCL2 (Thermo Fisher Scientific, Massachusetts, USA). To block CCL2, we used anti-CCL2 neutralizing antibodies (Sigma-Aldrich, Missouri, USA). All experiments were independently performed in triplicate. Detailed methods are described in Additional file 1.

Statistical analysis

The distribution of the data was assessed using the D’Agostino test. As the majority of the data were nonparametric, we used the Wilcoxon or Mann–Whitney test. P values were Bonferroni-corrected for the complete set of 19 variables, and a P-value < 0.0026 was accepted as significant. For the cellular in vitro migration assay, all experiments were independently performed in triplicate, and the results were compared with a t-test; a P-value < 0.05 was accepted as significant. To quantify associations between variables, we used Spearman or Pearson correlation. All analyses were performed using GraphPad Prism (GraphPad Software, La Jolla, CA, USA).

Results

The chemokine CCL2, but not other chemokines, is significantly increased during anaphylactic episodes

MCP chemokines CCL2/MCP-1, CCL7/MCP-3, CCL8/MCP-2, and CCL13/MCP-4

CCL2 concentrations measured during the anaphylactic episode (median 514 pg/ml) were significantly higher than those measured in convalescent serum samples collected later (median 80 days; 284 pg/ml; P < 0.0001; Fig. 1 and Table 2). This marked increase (median 106.0%; range: − 44.7% to 557.4%) was evident in 28/30 patients (Fig. 2). Serum CCL2 levels during the acute episode were also significantly higher than those observed in healthy subjects (median 279 pg/ml, P < 0.0001); however, CCL2 levels in convalescent samples showed no difference in comparison to CCL2 levels in healthy subjects (Fig. 1 and Table 2). Other MCP chemokines, including CCL7 (median 8.9, 8.5 and 8.1 pg/ml), CCL8 (73, 69 and 70 pg/ml) and CCL13 (113, 104 and 123 pg/ml), showed no differences during anaphylaxis or later compared to healthy subjects (Fig. 1 and Table 2).

Fig. 1
figure1

Serum CCL2, CCL5, CCL7, CCL8, CCL11, CCL13, CCL17, CCL21, CCL22, CCL24, CCL26, and tryptase levels in 30 patients during an acute anaphylactic episode and in convalescent samples collected later

Table 2 Laboratory data of anaphylactic patients and healthy subjects
Fig. 2
figure2

Comparison and correlation between serum CCL2 and tryptase levels in 30 patients with acute anaphylactic episodes

Eotaxin chemokines CCL11/eotaxin, CCL24/eotaxin-2 and CCL26/eotaxin-3

There were no differences in CCL11 (median 200, 211 and 160 pg/ml), CCL24 (1124, 946 and 1159 pg/ml) and CCL26 (1903, 1898 and 1877 pg/ml) between the acute and convalescent time points and the healthy subjects (Fig. 1 and Table 2).

Chemokines CCL5/Rantes, CCL17/TARC, CCL21/SLC and CCL22/MDC

There were no differences in CCL5 (median 40.9, 41.8 and 47.0 ng/ml), CCL17 (342, 303 and 344 pg/ml), CCL21 (1179, 1099 and 938 pg/ml) and CCL22 (666, 717 and 766 pg/ml) between the acute and convalescent time points and the healthy subjects (Fig. 1 and Table 2).

Increase in serum CCL2 levels highly correlates with an increase in serum tryptase

The median concentration of serum tryptase was significantly higher during the anaphylactic episode (12.9 µg/l) than later or in healthy subjects (5.4 and 3.3 µg/l, respectively; P ≤ 0.0005; Fig. 1 and Table 2). The median rate of increase of serum tryptase was 133.8% (range: − 6.6% to 893.4%; increase in 28/30 patients), which was comparable to the increase in serum CCL2 levels (Fig. 2). There was a significant positive correlation between the rates of increase of serum CCL2 and tryptase (r = 0.68, P < 0.0001) and between the acute concentration of serum CCL2 and the acute concentration of serum tryptase (r = 0.77, P < 0.0001; Fig. 2).

Anaphylactic episodes involve a substantial reduction in circulating basophils

Basophils, monocytes, lymphocytes, and PMNs

The absolute number of circulating basophils was significantly lower during the anaphylactic episode (median 5.0 cells/µl) than in convalescent blood samples collected later (19.1 cells/µl, P < 0.0001; Fig. 3 and Table 2). This decrease (median 65.6%, range 30.0–98.6%) was evident in all patients. There were no significant differences in the monocyte (median 396 and 441 cells/µl), lymphocyte (1378 and 1461 cells/µl), and PMN (3881 and 2875 cells/µl) absolute cell counts during the acute episode compared to convalescent blood samples collected later (Fig. 3).

Fig. 3
figure3

Absolute basophil, monocyte, lymphocyte and PMN counts and whole blood FCER1A, CPA3, and HDC gene expression in 26 patients during the acute anaphylactic episode and in convalescent samples collected later. PMNs polymorphonuclear leukocytes, FCER1A α subunit of the high-affinity IgE receptor, CPA3 carboxypeptidase A3, HDC histidine decarboxylase

Gene expression of basophil markers

We observed significantly lower whole blood gene expression of FCER1A, CPA3, and HDC during the anaphylactic episode than in convalescent samples (respectively; P ≤ 0.0018; Fig. 3 and Table 2). Acute whole blood gene expression of FCER1A, CPA3, and HDC significantly correlated with the acute absolute number of circulating basophils (r = 0.53, 0.79 and 0.81, respectively; P ≤ 0.005; Additional file 1: Fig. S1).

Anaphylactic serum enhances the in vitro migration of basophils via CCL2-dependent chemotactic activity

A basophil migration assay was performed using MACS-separated human basophils and a modified Boyden chamber, with quantification by absolute flow cytometry basophil counts. Basophils from all healthy donors showed high surface expression of CCR2 (Table 2). All experiments were performed independently in triplicate (detailed information is provided in Additional file 1).

Basophil migration induced by HBSS and rCCL2

As shown in Fig. 4a, during a 150-min incubation time with Hank’s balanced salt solution (HBSS), only a small number of basophils (mean, SD), 0.8 ± 0.7%) transmigrated across the polycarbonate membrane. Basophil migration was significantly enhanced by the presence of 10 nM rCCL2 and 50 nM rCCL2 (8.1 ± 4.0% and 14.0 ± 8.1%; 150 min of incubation); however, after blocking with anti-CCL2 mAbs, rCCL2-induced migration was almost completely inhibited (0.8 ± 0.6%, P = 0.036 and 0.8 ± 0.1%, P = 0.047, blocking at 10 nM and 50 nM of rCCL2, respectively).

Fig. 4
figure4

ac Effects of CCL2 and acute and convalescent serum from patients with an anaphylactic episode on basophil in vitro migration. Basophil migration after 150 min of incubation: a in the presence of rCCL2 in the lower wells and after CCL2 blocking and b in the presence of acute or convalescent serum in the lower wells and after CCL2 blocking. c Time course of basophil migration (after 30, 60, 90, 120, and 150 min of incubation) in the presence of acute and convalescent serum in the lower wells. All experiments were independently performed in triplicate, with a basophils from 5 healthy donors; b basophils from the same 5 healthy donors and serum samples from 5 patients and c basophils from 3 healthy donors and serum samples from 3 patients (details in Additional file 1: Table S1). HBSS Hank’s balanced salt solution

Basophil migration induced by anaphylactic and convalescent serum

We compared the effects of acute serum collected during the anaphylactic episode and convalescent serum collected later (Table 2) on basophil migration. After 150 min of incubation, the number of transmigrated basophils was significantly higher (twofold) in the presence of acute serum in the lower wells than in the presence of convalescent serum in the lower wells (mean, SD: 54.0 ± 19.3% vs. 28.3 ± 11.7%, respectively; P = 0.01) (Fig. 4b). The number of transmigrated cells increased linearly until 150 min of incubation and then plateaued (Fig. 4c). A neutralizing antibody against CCL2 significantly blocked basophil transmigration induced by anaphylactic serum (37.7 ± 20.8% vs. 26.1 ± 19.7%; P = 0.001). However, a neutralizing antibody against CCL2 did not show any blocking effect on the chemotactic response induced by convalescent serum (32.5 ± 12.5% vs. 30.7 ± 18.3%) (Fig. 4b).

Discussion

Our study demonstrated that there is a selective and significant increase in serum CCL2 chemokine levels during anaphylactic reactions. No significant changes were observed for other chemokines, which were previously implicated in different allergic diseases or during allergic inflammation [15,16,17,18,19,20,21,22,23,24,25]. Thus, the chemokine patterns of CCL5, CCL7, CCL8, CCL11, CCL13, CCL17, CCL21, CCL22, CCL24, and CCL26 might be of limited importance for anaphylaxis. While activation of the pathways associated with multiple inflammatory cytokines, including IL-2, IL-6, IL-10, and TNFRI, were observed during anaphylaxis [6, 9], the selective CCL2 chemokine cascade might be important for chemotactic activity during anaphylactic reactions. It was recently reported that the CCL2-FcεRI-histone deacetylase 3 signalling axis mediates passive anaphylaxis by increasing the expression of CCL2 in mast cells [28, 29]. After allergen stimulation, histone deacetylase 3 binds to FcεRI, and histone deacetylase 3 increases the expression of SP1 and C-Jun, which bind to the promoter sequences of CCL2 to increase the expression of CCL2 [28, 29]. Conversely, in the absence of allergen stimulation, histone deacetylase 3 binds to the promoter sequences of CCL2 to suppress the expression of CCL2 [28].

Our study design and the median time between symptom onset and sample collection were highly comparable with those of previous studies of anaphylaxis [3, 6, 7, 9, 30]. This suggests that this is an unbiased comparison, including the confirmation that the chemokines CCL5 and CCL11, which may affect other important effector cells of allergic inflammation such as eosinophils, are not induced during anaphylaxis [6, 7]. The nature of the management of anaphylaxis (including administration of high-dose corticosteroids) makes it difficult to exclude the potential confounding effects of treatment. However, it was previously demonstrated that serum CCL2, CCL5, and CCL11 levels are not affected by corticosteroid treatment [7]. Nevertheless, corticosteroid treatment or the time between symptom onset and sample collection may have affected the levels of the other measured chemokines.

In the present study, we could not determine the cellular sources of CCL2 during anaphylaxis. However, we showed a highly significant positive correlation between elevated blood levels of acute CCL2 and tryptase and strong similarities between the percentage increases of CCL2 and tryptase from convalescent serum samples. Tryptase is largely mast cell-derived, and mature β-tryptase is stored in mast cell granules and released upon mast cell activation during acute anaphylaxis [2, 5,6,7]. Therefore, it is tempting to speculate that the blood CCL2 increase that occurs during anaphylaxis is IgE related and mainly mast cell derived. In vitro activation of human mast cells by anti-IgE induces secretion of CCL2 after 30 min of stimulation, and this increase is observed earlier than TNF-α, IL-13, or GM-CSF mast cell secretion, peaking 90 min after anti-IgE stimulation [31]. Furthermore, mast cell CCL2 secretion is induced at low allergen concentrations or in the context of low receptor occupancy with IgE [32], and due to the short time frame within which the increase in serum CCL2 was observed in the current and previous studies [7], rapid induction of CCL2 production by the allergen-IgE axis might be feasible. Nevertheless, CCL2 is produced by a variety of cell types, including endothelial cells and smooth muscle cells [33], astrocytes as a major source of CCL2 during central nervous system inflammation [34] and cancer and stromal cells as a major source of CCL2 in tumour microenvironments [35]; thus, the cellular sources of CCL2 during anaphylaxis are currently unknown. Additional and substantially studies of mast cell CCL2 expression and secretion are required to confirm this speculation.

The results of experimental allergen challenge in the nose, airways, and skin have demonstrated that there is an influx of basophils to inflammatory sites several hours after allergen exposure [36,37,38,39]. Furthermore, it was recently demonstrated that airway allergen challenge induces TLR-dependent CCL2 production in the lungs and that circulating basophils are recruited to the lungs by CCL2-mediated transendothelial migration and a chemotactic gradient [40]. Our study demonstrated significantly enhanced CCL2-mediated chemotactic activity of anaphylactic serum for the migration of isolated basophils. Conversely, no CCL2-mediated basophil chemotactic activity was observed for the convalescent serum collected later after the reaction. The CCL2-mediated basophil chemotactic activity of anaphylactic serum and the reduction in circulating basophils during anaphylaxis, coupled with the previous finding that basophils are the granulocytes most resistant to apoptosis [41], suggest that anaphylaxis induces rapid CCL2-mediated basophil migration rather than elimination by apoptosis. Moreover, anaphylaxis-related basophil migration appears to be selective because no significant changes were observed for monocytes, lymphocytes, PMNs, or chemokines that may affect other effector cells, and the decreased gene expression of basophil markers FCER1A, CPA3 and HDC corroborates the flow cytometry data. Therefore, it is tempting to speculate that CCL2 might be mast cell derived and that circulating basophils influx to the sites where the activation and degranulation of mast cells occur, thereby contributing to the clinical presentation of the sites of allergic reaction. This is consistent with clinical observations of different severities and end-organ patterns of anaphylaxis, which suggest that local rather than generalized mast cell and/or basophil degranulation may predominate in some individuals [41]. However, a substantially broader assessment is needed to explore and confirm CCL2-mediated cellular crosstalk during acute allergic reactions.

Although CCL2 displays major chemotactic activity for monocytes and interferes with the egress of monocytes from the bone marrow to the circulation during homeostasis and inflammation [42], no changes in circulating monocytes were observed during anaphylaxis. However, studies in mice have shown that depletion of monocytes/macrophages can reduce anaphylaxis in both IgG-mediated passive models and active models [2, 11].

Conclusion

In conclusion, our data suggest that during anaphylaxis, an increase in the chemokine CCL2 occurs, which correlates with CCL2-mediated chemotactic activity in basophils and substantial migration of circulating basophils. Our findings imply an important and specific role for CCL2 in the pathophysiology of human anaphylaxis.

Availability of data and materials

Raw data were generated at the University Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia. Derived data supporting the findings of this study are available from the corresponding author upon reasonable request.

Abbreviations

CCL:

C-C Motif Chemokine Ligand

CCR:

C-C motif chemokine receptor

CPA:

Carboxypeptidase A3

FCER1A:

α subunit of the high-affinity IgE receptor

HBSS:

Hank’s balanced salt solution

HDC:

l-Histidine decarboxylase

MCP:

Monocyte chemoattractant protein

MDC:

Macrophage-Derived Chemokine

PMNs:

Polymorphonuclear leukocytes

SLC:

Secondary Lymphoid Tissue Chemokine

TARC:

Thymus and Activation Regulated Chemokine

References

  1. 1.

    Muraro A, Roberts G, Worm M, Bilò MB, Brockow K, Fernández Rivas M, et al. Anaphylaxis: guidelines from the European Academy of Allergy and Clinical Immunology. Allergy Eur J Allergy Clin Immunol. 2014;69(8):1026–45.

    CAS  Article  Google Scholar 

  2. 2.

    Reber LL, Hernandez JD, Galli SJ. The pathophysiology of anaphylaxis. J Allergy Clin Immunol. 2017;140:335–48.

    CAS  Article  Google Scholar 

  3. 3.

    Vadas P, Gold M, Perelman B, Liss GM, Lack G, Blyth T, et al. Platelet-activating factor, PAF acetylhydrolase, and severe anaphylaxis. N Engl J Med. 2008;358:28–35.

    CAS  Article  Google Scholar 

  4. 4.

    Korošec P, Gibbs BF, Rijavec M, Custovic A, Turner PJ. Important and specific role for basophils in acute allergic reactions. Clin Exp Allergy. 2018;48(5):502–12.

    Article  Google Scholar 

  5. 5.

    Schwartz LB. Diagnostic value of tryptase in anaphylaxis and mastocytosis. Immunol Allergy Clin North Am. 2006;26(3):451–63.

    Article  Google Scholar 

  6. 6.

    Brown SGA, Stone SF, Fatovich DM, Burrows SA, Holdgate A, Celenza A, et al. Anaphylaxis: clinical patterns, mediator release, and severity. J Allergy Clin Immunol. 2013;132:1141–9.

    CAS  Article  Google Scholar 

  7. 7.

    Korosec P, Turner PJ, Silar M, Kopac P, Kosnik M, Gibbs BF, et al. Basophils, high-affinity IgE receptors, and CCL2 in human anaphylaxis. J Allergy Clin Immunol. 2017;140:750–8.

    CAS  Article  Google Scholar 

  8. 8.

    Ono E, Taniguchi M, Mita H, Fukutomi Y, Higashi N, Miyazaki E, et al. Increased production of cysteinyl leukotrienes and prostaglandin D2 during human anaphylaxis. Clin Exp Allergy. 2009;39(1):72–80.

    CAS  Article  Google Scholar 

  9. 9.

    Stone SF, Cotterell C, Isbister GK, Holdgate A, Brown SGA. Elevated serum cytokines during human anaphylaxis: identification of potential mediators of acute allergic reactions. J Allergy Clin Immunol. 2009;124:786.e4–792.e4.

    Article  Google Scholar 

  10. 10.

    Iikura M, Ebisawa M, Yamaguchi M, Tachimoto H, Ohta K, Yamamoto K, et al. Transendothelial migration of human basophils. J Immunol. 2004;173:5189–95.

    CAS  Article  Google Scholar 

  11. 11.

    Balbino B, Sibilano R, Starkl P, Marichal T, Gaudenzio N, Karasuyama H, et al. Pathways of immediate hypothermia and leukocyte infiltration in an adjuvant-free mouse model of anaphylaxis. J Allergy Clin Immunol. 2017;139:584.e10–596.e10.

    Article  Google Scholar 

  12. 12.

    Jönsson F, Mancardi DA, Albanesi M, Bruhns P. Neutrophils in local and systemic antibody-dependent inflammatory and anaphylactic reactions. J Leukoc Biol. 2013;94:643–56. https://doi.org/10.1189/jlb.1212623.

    CAS  Article  PubMed  Google Scholar 

  13. 13.

    Francis A, Bosio E, Stone SF, Fatovich DM, Arendts G, Nagree Y, et al. Neutrophil activation during acute human anaphylaxis: analysis of MPO and sCD62L. Clin Exp Allergy. 2017;47:361–70.

    CAS  Article  Google Scholar 

  14. 14.

    Kasperska-Zajaç A, Rogala B. Platelet function in anaphylaxis. J Investig Allergol Clin Immunol. 2006;16:1–4.

    PubMed  Google Scholar 

  15. 15.

    Kuo C-H, Collins AM, Boettner DR, Yang Y, Ono SJ. Role of CCL7 in type I hypersensitivity reactions in murine experimental allergic conjunctivitis. J Immunol. 2017;198:645–56.

    CAS  Article  Google Scholar 

  16. 16.

    Debes GF, Diehl MC. CCL8 and skin T cells-an allergic attraction. Nat Immunol. 2011;12:111–2.

    CAS  Article  Google Scholar 

  17. 17.

    Baumann R, Rabaszowski M, Stenin I, Tilgner L, Scheckenbach K, Wiltfang J, et al. Comparison of the nasal release of IL-4, IL-10, IL-17, CCL13/MCP-4, and CCL26/eotaxin-3 in allergic rhinitis during season and after allergen challenge. Am J Rhinol Allergy. 2013;27:266–72.

    Article  Google Scholar 

  18. 18.

    Luster AD. Antichemokine immunotherapy for allergic diseases. Curr Opin Allergy Clin Immunol. 2001;1:561–7.

    CAS  Article  Google Scholar 

  19. 19.

    Gaspar K, Kukova G, Bunemann E, Buhren BA, Sonkoly E, Szollosi AG, et al. The chemokine receptor CCR3 participates in tissue remodeling during atopic skin inflammation. J Dermatol Sci. 2013;71:12–21.

    CAS  Article  Google Scholar 

  20. 20.

    Esaki H, Takeuchi S, Furusyo N, Yamamura K, Hayashida S, Tsuji G, et al. Levels of immunoglobulin E specific to the major food allergen and chemokine (C-C motif) ligand (CCL)17/thymus and activation regulated chemokine and CCL22/macrophage-derived chemokine in infantile atopic dermatitis on Ishigaki Island. J Dermatol. 2016;43:1278–82.

    CAS  Article  Google Scholar 

  21. 21.

    Ahrens B, Schulz G, Bellach J, Niggemann B, Beyer K. Chemokine levels in serum of children with atopic dermatitis with regard to severity and sensitization status. Pediatr Allergy Immunol. 2015;26:634–40.

    Article  Google Scholar 

  22. 22.

    Hulshof L, Overbeek SA, Wyllie AL, Chu MLJN, Bogaert D, de Jager W, et al. Exploring immune development in infants with moderate to severe atopic dermatitis. Front Immunol. 2018;9:630.

    Article  Google Scholar 

  23. 23.

    Watanabe H. Review article recent advances in drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic symptoms. J Immunol Res. 2018. https://doi.org/10.1155/2018/5163129.

    Article  PubMed  PubMed Central  Google Scholar 

  24. 24.

    Eberhard Y, Ortiz S, Lascano AR, Kuznitzky R, Serra HM. Up-regulation of the chemokine CCL21 in the skin of subjects exposed to irritants. BMC Immunol. 2004;8:1–8.

    Google Scholar 

  25. 25.

    He H, Li R, Choi S, Zhou L, Pavel A, Estrada YD, et al. Increased cardiovascular and atherosclerosis markers in blood of older patients with atopic dermatitis. Ann Allergy Asthma Immunol. 2020;124:70–8.

    CAS  Article  Google Scholar 

  26. 26.

    Mueller UR. Insect sting allergy: clinical picture, diagnosis and treatment. New York: Gustav Fischer; 1990.

    Google Scholar 

  27. 27.

    Čelesnik N, Vesel T, Rijavec M, Šilar M, Eržen R, Košnik M, et al. Short-term venom immunotherapy induces desensitization of FcεRI-mediated basophil response. Allergy Eur J Allergy Clin Immunol. 2012;67:1594–600.

    Google Scholar 

  28. 28.

    Kim Y, Kim K, Park D, Lee E, Lee H, Lee YS, et al. Histone deacetylase 3 mediates allergic skin inflammation by regulating expression of MCP1 protein. J Biol Chem. 2012;287(31):25844–59.

    CAS  Article  Google Scholar 

  29. 29.

    Kim M, Kwon Y, Jung HS, Kim Y, Jeoung D. FcεRI-HDAC3-MCP1 signaling axis promotes passive anaphylaxis mediated by cellular interactions. Int J Mol Sci. 2019;20(19):4964.

    CAS  Article  Google Scholar 

  30. 30.

    Lin RY, Schwartz LB, Curry A, Pesola GR, Knight RJ, Lee HS, et al. Histamine and tryptase levels in patients with acute allergic reactions: an emergency department-based study. J Allergy Clin Immunol. 2000;106:65–71.

    CAS  Article  Google Scholar 

  31. 31.

    Gaudenzio N, Sibilano R, Marichal T, Starkl P, Reber LL, Cenac N, et al. Different activation signals induce distinct mast cell degranulation strategies. J Clin Invest. 2016;126(10):3981–98.

    Article  Google Scholar 

  32. 32.

    Gonzalez-Espinosa C, Odom S, Olivera A, Hobson JP, Martinez MEC, Oliveira-dos-Santos A, et al. Preferential signaling and induction of allergy-promoting lymphokines upon weak stimulation of the high affinity IgE receptor on mast cells. J Exp Med. 2003;197(11):1453–65.

    CAS  Article  Google Scholar 

  33. 33.

    Melgarejo E, Medina MÁ, Sánchez-Jiménez F, Urdiales JL. Monocyte chemoattractant protein-1: a key mediator in inflammatory processes. Int J Biochem Cell Biol. 2009;41(5):998–1001.

    CAS  Article  Google Scholar 

  34. 34.

    Yao Y, Tsirka SE. Monocyte chemoattractant protein-1 and the blood–brain barrier. Cell Mol Life Sci. 2014;71(4):683–97.

    CAS  Article  Google Scholar 

  35. 35.

    Yoshimura T. The production of monocyte chemoattractant protein-1 (MCP-1)/CCL2 in tumor microenvironments. Cytokine. 2017;98:71–8.

    CAS  Article  Google Scholar 

  36. 36.

    Iliopoulos O, Baroody FM, Naclerio RM, Bochner BS, Kagey-Sobotka A, Lichtenstein LM. Histamine-containing cells obtained from the nose hours after antigen challenge have functional and phenotypic characteristics of basophils. J Immunol. 1992;148:2223–8.

    CAS  PubMed  Google Scholar 

  37. 37.

    Guo CB, Liu MC, Galli SJ, Bochner BS, Kagey-Sobotka A, Lichtenstein LM. Identification of IgE-bearing cells in the late-phase response to antigen in the lung as basophils. Am J Respir Cell Mol Biol. 1994;10:384–90.

    CAS  Article  Google Scholar 

  38. 38.

    Irani AM, Huang C, Xia HZ, Kepley C, Nafie A, Fouda ED, et al. Immunohistochemical detection of human basophils in late-phase skin reactions. J Allergy Clin Immunol. 1998;101:354–62.

    CAS  Article  Google Scholar 

  39. 39.

    Gauvreau GM, Lee JM, Watson RM, Irani AM, Schwartz LB, O’Byrne PM. Increased numbers of both airway basophils and mast cells in sputum after allergen inhalation challenge of atopic asthmatics. Am J Respir Crit Care Med. 2000;161:1473–8.

    CAS  Article  Google Scholar 

  40. 40.

    Lv J, Yu Q, Lv J, Di C, Lin X, Su W, et al. Airway epithelial TSLP production of TLR2 drives type 2 immunity in allergic airway inflammation. Eur J Immunol. 2018;48(11):1838–50.

    CAS  Article  Google Scholar 

  41. 41.

    Simons FER, Frew AJ, Ansotegui IJ, Bochner BS, Golden DBK, Finkelman FD, et al. Risk assessment in anaphylaxis: current and future approaches. J Allergy Clin Immunol. 2007;120:S2–24.

    CAS  Article  Google Scholar 

  42. 42.

    Serbina NV, Pamer EG. Monocyte emigration from bone marrow during bacterial infection requires signals mediated by chemokine receptor CCR2. Nat Immunol. 2006;7(3):311–7.

    CAS  Article  Google Scholar 

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Acknowledgements

Not applicable.

Funding

The research was supported by the Slovenian Research Agency (Grant Nos. P3-0360 and 39238).

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Authors

Contributions

PKorosec, RV and AK designed the study. PKopac and RE evaluated the patients and revised the manuscript. RV, MRihar, AK, MRijavec, and UBS performed laboratory tests and experiments and revised the manuscript. PKorosec and RV wrote the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Peter Korosec.

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The study was approved by the Slovenian National Medical Ethics Committee (0120-295/2017/3). All subjects gave written informed consent to participate in the study.

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The authors declare that they have no competing interests.

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Supplementary information

Additional file 1.

Additional methods and results. Table S1. Detailed information on the number of participants for whom we assessed different laboratory parameters. Additional results. Figure S1. Correlation between absolute basophil counts and whole-blood FCER1A, CPA3, and HDC gene expression in 26 anaphylactic patients

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Vantur, R., Rihar, M., Koren, A. et al. Chemokines during anaphylaxis: the importance of CCL2 and CCL2-dependent chemotactic activity for basophils. Clin Transl Allergy 10, 63 (2020). https://doi.org/10.1186/s13601-020-00367-2

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Keywords

  • Anaphylaxis
  • Chemokines
  • CCL2
  • Tryptase
  • Basophils
  • Chemotaxis
  • Migration