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Allergen Encyclopedia
Table of Contents

Component

i216 Api m 5

i216 Api m 5 Scientific Information

Type:

Component

Name; WHO/IUIS:

Api m 5

Biological function:

Serine-peptidase, cleaves N-terminal dipeptides; conversion of promelittin into melittin

Allergen code:

i216

Molecular Weight:

100 kDa

Source Material:

Recombinant protein

Other Names :

Honey bee/Apis mellifera venom dipeptidyl peptidase IV

Summary  

Api m 5, a glycoprotein of the venom dipeptidyl peptidase IV (DPPIV) family, is a major allergen of Apis mellifera (honeybee) venom (HBV). It exhibits cross-reactivity with homologous Vespid venom DPPIV allergens. 

Epidemiology

Worldwide distribution

Api m 5 sensitization has a prevalence of 16% to 70% among HBV-allergic populations (reviewed in [1]). Thus, Api m 5 is considered a major allergen in HBV-allergic patients.

Environmental characteristics

Source and tissue

Api m 5 is secreted into the venom sac of Apis mellifera, where it contributes less than 1% of venom dry weight [2]. 

Risk factors

Sensitization to Api m 5 occurs through injection (bee sting). 

Clinical relevance

Cross-reactive molecules

Api m 5 belongs to the DPPIV family of allergens, which is widespread among Hymenoptera and contributes to cross-reactivity between these venoms [1, 2]. 

Disease severity

Various patterns of sensitization to HBV allergens have been described, but no clinical correlate of severity has been identified so far [1].

Molecular aspects

Biochemistry

Api m 5, also known as venom DPPIV, is a secreted glycoprotein with a molecular weight of 100 kDa (775 aminoacids), N-glycosylated side chains and disulfide bonds [1, 3, 4]. It cleaves N-terminal dipeptides, one of its substrates being promelittin thus generating the active melittin molecule [1].

Isoforms, epitopes, antibodies

As of July 5, 2023, a unique isoallergen, Api m 5.0101, has been included in the World Health Organization (WHO) and International Union of Immunological Societies (IUIS) Allergen Nomenclature [5]. 

Cross-reactivity due to structural similarity

Api m 5 and its Vespid counterparts such as Ves v 3 and Pol d 3 exhibit clinically relevant cross-reactivity [1].

Diagnostic relevance

Cross-reactivity between HBV and Vespid venoms

Cross-reactivity between Api m 5 and its homologous Vespid DPPIV allergens contribute to the double-positivity to HBV and Vespid venom whole extracts [1, 6].

Disease Severity

In Hymenoptera IgE testing, the quantitative result of specific IgE to a molecular allergen or whole venom extract is neither predictive of, nor correlated to the severity of the reaction [1]. 

Sensitivity of in vitro assays

The prevalence of sensitization to individual HBV allergens, including Api m 5, in HBV-allergic patients varies depending on multiple factors such as geography, patient inclusion criteria, single or double positivity to HBV and Vespid venoms, underlying sensitization profile, use of a recombinant allergen versus a natural purified allergen, and the assay format [1, 7, 8]. Thus, the diagnostic sensitivity of specific IgE to rApi m 5 ranges from 16 to 70% in HBV-allergic patients [1].  Using a panel of HBV allergens including rApi m 5 besides available HBV marker allergens Api m 1, Api m 3, and Api m 10 improves the rate of confirmation of genuine HBV sensitization [1, 7, 8]. 

Api m 5 sensitization can be detected with commercially available singleplex methods.

Diagnostic specificity

The diagnostic specificity of IgE to rApi m 5 in HBV-allergic patients was reported as 100% when compared to HBV-negative controls [7]. Detectable rApi  5-specific IgE were found in 3/40 (7.5%) cases of Vespid venom allergic patients without HBV allergy, and in 2/6 (30%) of nonallergic controls sensitized to HBV extract [8]. 

 

Compiled by:

Author: Prof. Joana Vitte

Reviewer: Dr. Merima Mehic Chaveton

References

1. Dramburg S, Hilger C, Santos AF, de Las Vecillas L, Aalberse RC, Acevedo N, et al. EAACI Molecular Allergology User's Guide 2.0. Pediatr Allergy Immunol. 2023;34 Suppl 28:e13854.

2. Spillner E, Blank S, Jakob T. Hymenoptera allergens: from venom to "venome". Front Immunol. 2014;5:77.

3. UniProt. UniProt B2D0J4 for Api m 5 2023 [Available from: https://www.uniprot.org/uniprotkb/B2D0J4/entry.

4. Blank S, Seismann H, Bockisch B, Braren I, Cifuentes L, McIntyre M, et al. Identification, recombinant expression, and characterization of the 100 kDa high molecular weight Hymenoptera venom allergens Api m 5 and Ves v 3. J Immunol. 2010;184(9):5403-13. 

5. IUIS/WHO. IUIS/WHO Apis mellifera 2023 [Available from: http://allergen.org/search.php?allergenname=&allergensource=apis+mellifera&TaxSource=&TaxOrder=&foodallerg=all&bioname=.

6. Jovanovic D, Peric-Popadic A, Djuric V, Stojanovic M, Lekic B, Milicevic O, et al. Molecular diagnostics and inhibition of cross-reactive carbohydrate determinants in Hymenoptera venom allergy. Clin Transl Allergy. 2023;13(3):e12230.

7. Vachova M, Panzner P, Kopac P, Bidovec Stojkovic U, Korosec P. Routine clinical utility of honeybee venom allergen components. J Allergy Clin Immunol Pract. 2018;6(6):2121-3 e1.

8. Kohler J, Blank S, Muller S, Bantleon F, Frick M, Huss-Marp J, et al. Component resolution reveals additional major allergens in patients with honeybee venom allergy. J Allergy Clin Immunol. 2014;133(5):1383-9, 9 e1-6.