Original Article

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Blood Res 2018; 53(4):

Published online December 31, 2018

https://doi.org/10.5045/br.2018.53.4.299

© The Korean Society of Hematology

Neutrophil oxidative burst as a diagnostic indicator of IgG-mediated anaphylaxis

Dong Il Won1*, Sujeong Kim2, and Eun Hee Lee3

1Department of Clinical Pathology, School of Medicine, Kyungpook National University, Daegu, Korea.

2Division of Allergy and Infectious Diseases, Department of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Korea.

3Green Cross Reference Laboratory, Yongin, Korea.

Correspondence to : Correspondence to Dong Il Won, M.D., Ph.D. Department of Clinical Pathology, Kyungpook National University School of Medicine, 130 Dongdeok-ro, Jung-gu, Daegu 41944, Korea. wondi@knu.ac.kr

Received: June 24, 2018; Revised: July 26, 2018; Accepted: July 30, 2018

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

IgG-mediated anaphylaxis occurs after infusion of certain monoclonal antibody-based therapeutics. New in vitro tests are urgently needed to diagnose such reactions. We investigated whether allergens trigger neutrophil oxidative burst (OB) and if neutrophil OB occurs due to allergen-specific IgG (sIgG).

Methods

Neutrophil OB was measured by dihydrorhodamine 123 flow cytometry using a leukocyte suspension spiked with a very small patch of the allergen crude extract, Dermatophagoides farinae (Der f). The mean fluorescence intensity ratio of stimulated to unstimulated samples was calculated as the neutrophil oxidative index (NOI).

Results

The Der f-specific NOI (Der f-sNOI) showed a time-dependent increase after Der f extract addition. At 15 min activation, higher Der f-sIgG levels were associated with lower Der f-sNOI values in 31 subjects (P<0.05). This inverse relationship occurs due to the initial blocking effect of free Der f-sIgG. Additionally, neutrophil OB was nearly absent (Der f-sNOI of −1) in two cases: a subject with undetectable Der f-sIgG levels and washed leukocyte suspensions deprived of Der f-sIgG.

Conclusion

Allergens can trigger neutrophil OB via preexisting allergen-sIgG. Neutrophil OB can be easily measured in a leukocyte suspension spiked with the allergen. This assay can be used to diagnose IgG-mediated anaphylaxis.

Keywords Neutrophils, Oxidative burst, Anaphylaxis, Immunoglobulin G, Dihydrorhodamine 123

Article

Original Article

Blood Res 2018; 53(4): 299-306

Published online December 31, 2018 https://doi.org/10.5045/br.2018.53.4.299

Copyright © The Korean Society of Hematology.

Neutrophil oxidative burst as a diagnostic indicator of IgG-mediated anaphylaxis

Dong Il Won1*, Sujeong Kim2, and Eun Hee Lee3

1Department of Clinical Pathology, School of Medicine, Kyungpook National University, Daegu, Korea.

2Division of Allergy and Infectious Diseases, Department of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Korea.

3Green Cross Reference Laboratory, Yongin, Korea.

Correspondence to:Correspondence to Dong Il Won, M.D., Ph.D. Department of Clinical Pathology, Kyungpook National University School of Medicine, 130 Dongdeok-ro, Jung-gu, Daegu 41944, Korea. wondi@knu.ac.kr

Received: June 24, 2018; Revised: July 26, 2018; Accepted: July 30, 2018

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

IgG-mediated anaphylaxis occurs after infusion of certain monoclonal antibody-based therapeutics. New in vitro tests are urgently needed to diagnose such reactions. We investigated whether allergens trigger neutrophil oxidative burst (OB) and if neutrophil OB occurs due to allergen-specific IgG (sIgG).

Methods

Neutrophil OB was measured by dihydrorhodamine 123 flow cytometry using a leukocyte suspension spiked with a very small patch of the allergen crude extract, Dermatophagoides farinae (Der f). The mean fluorescence intensity ratio of stimulated to unstimulated samples was calculated as the neutrophil oxidative index (NOI).

Results

The Der f-specific NOI (Der f-sNOI) showed a time-dependent increase after Der f extract addition. At 15 min activation, higher Der f-sIgG levels were associated with lower Der f-sNOI values in 31 subjects (P<0.05). This inverse relationship occurs due to the initial blocking effect of free Der f-sIgG. Additionally, neutrophil OB was nearly absent (Der f-sNOI of −1) in two cases: a subject with undetectable Der f-sIgG levels and washed leukocyte suspensions deprived of Der f-sIgG.

Conclusion

Allergens can trigger neutrophil OB via preexisting allergen-sIgG. Neutrophil OB can be easily measured in a leukocyte suspension spiked with the allergen. This assay can be used to diagnose IgG-mediated anaphylaxis.

Keywords: Neutrophils, Oxidative burst, Anaphylaxis, Immunoglobulin G, Dihydrorhodamine 123

Fig 1.

Figure 1.

Flow cytometry data acquisition and analysis for oxidative burst in response to Der f extract. Calculations of NOI and ΔFSC are described in the Materials and Methods section.

Abbreviations: Der f, Dermatophagoides farinae; FSC, forward scatter; MFI, mean fluorescence intensity; NOI, neutrophil oxidative index; SSC, side scatter.

Blood Research 2018; 53: 299-306https://doi.org/10.5045/br.2018.53.4.299

Fig 2.

Figure 2.

Time course experiments showing effects of activation period on neutrophil reaction against Der f extract. Measurements were performed from 0 min (just prior to addition) to 40 min after adding Der f extract in 10 min intervals (total of five times). The typical results of four separate experiments are shown. (A) Raw data of FSC and MFI values. The difference between stimulated values and unstimulated values was significant (P<0.05) starting at 10 min activation for both FSC and MFI. Asterisks indicate significant stimulated values. (B) Calculated indices (ΔFSC and NOI). The linearity of Der f-sNOI values according to the activation time was significant (P<0.01, asterisk), which was not observed for the ΔFSC values.

Abbreviations: Der f, Dermatophagoides farinae; FSC, forward scatter; MFI, mean fluorescence intensity; NOI, neutrophil oxidative index; SSC, side scatter.

Blood Research 2018; 53: 299-306https://doi.org/10.5045/br.2018.53.4.299

Fig 3.

Figure 3.

Correlation between Der f-sNOI vs. ΔFSC measured at 15 min activation in the 31 enrolled subjects. Correlation between Der f-sNOI and ΔFSC measured at 15 min after activation in the 31 enrolled subjects. ΔFSC was significantly correlated with Der f-sNOI (P<0.00005).

Blood Research 2018; 53: 299-306https://doi.org/10.5045/br.2018.53.4.299

Fig 4.

Figure 4.

Blood levels of Der f-sIgG (total) in 31 subjects and their correlation with (A) subject age (P<0.05); (B) Der f-sIgE level; and (C) Der f-sIgG4 level. In the panel C, IgG4 levels of five subjects with less than the limit of detection (0.1 µg/mL) were assumed to be 0.05 µg/mL for convenience. The red and blue arrows indicate extreme cases of Der f-sIgG levels (highest and lowest, respectively). In panel A, the case with the lowest (undetectable) Der f-sIgG levels (73-year-old woman, potential non-responder against Der f) was excluded from the regression analysis.

Blood Research 2018; 53: 299-306https://doi.org/10.5045/br.2018.53.4.299

Fig 5.

Figure 5.

Der f-sNOI and Der f-sΔFSC according to the Der f-sIgG level. The relationship between Der f-sIgG levels and (A) NOI; (B) 1/NOI (P<0.05); and (C) ΔFSC (P=0.201). The red and blue arrows indicate extreme cases of Der f-sIgG levels (highest and lowest, respectively). In panel B, the case with the lowest (undetectable) Der f-sIgG levels (73-year-old woman, potential non-responder against Der f) was excluded from the regression analysis.

Blood Research 2018; 53: 299-306https://doi.org/10.5045/br.2018.53.4.299

Fig 6.

Figure 6.

Der f-sNOI and its relationship with (A) Der f-sIgG4; (B) Der f-sBAT; (C) Der f-sIgE; and (D) subject's age (P=0.157). No significant relationships were found. The red and blue arrows indicate extreme cases of Der f-sIgG levels (highest and lowest, respectively).

Abbreviations: BAT, basophil activation test; Der f, Dermatophagoides farinae; NOI, neutrophil oxidative index.

Blood Research 2018; 53: 299-306https://doi.org/10.5045/br.2018.53.4.299
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