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Fish Allergenicity Ladder and Parvalbumin Epitopes for Predicting Clinical Cross-reactivity and Reintroduction
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Background: IgE-mediated fish allergy has long been considered
an umbrella term due to the high cross-reactivity of parvalbumin, the
major fish allergen. Yet, clinical tolerance to certain fish highlights
allergenicity differences. In this study, we sought to construct a fish
allergenicity ladder and identify fish parvalbumin epitopes to improve
the diagnosis of fish allergy. Methods: Reported clinical
history and the serum-specific IgE (sIgE) responses of 200 fish allergic
patients were collected and analyzed, while the relative parvalbumin
content in different fish were measured for the construction of fish
allergenicity ladder. Double-blind placebo-controlled food challenge
(DBPCFC) and open challenge against salmon, grass carp and grouper were
performed in 58 selected patients for validation of the ladder. Epitope
mapping was performed by peptide array against parvalbumins of salmon
(both β-1 and β-2), cod, grouper, and grass carp with sera from fish
allergic (n=11), partial fish tolerant (n=12), and complete fish
tolerant (n=5) patients diagnosed based on oral food challenge outcome.
Results: The distribution pattern of clinical, sIgE and
molecular data and their strong positive correlation led to the
construction of a 4-step fish allergenicity ladder comprising: step 1 of
the least allergenic fishes (tuna, halibut, salmon), steps 2 (cod) and 3
(herring and grouper) of moderately allergenic fishes to step 4 of
highly allergenic fishes (catfish, grass carp and tilapia). Epitope
mapping revealed one epitope from grouper parvalbumin (AA64-78) for
diagnosing general fish allergy and one epitopic region from salmon
parvalbumin (AA19-33) as biomarker of specific fish tolerance. Only
epitope-specific IgE differentiated these patients but not sIgE to fish
extract or parvalbumin. Conclusion: The fish ladder and
epitopes discovery can precisely differentiate fish-allergic and
tolerant subjects and guide fish reintroduction by stepping up the
ladder, which innovate fish allergy care in the next millennium.
Wiley
Christine Yee Yan Wai
Nicki Y.H. Leung
Agnes Sze Yin Leung
Man Fung Tang
Asa Marknell-DeWitt
Jaime Rosa Duque
Gilbert Chua
Yat S. Yau
Wai Hung Chan
Po K. Ho
Mike Kwan YW
Qun U. Lee
Joshua S.C. Wong
Ivan C.S. Lam
James W.C.H. Cheng
David C.K. Luk
Zhongyi Liu
Noelle Anne Ngai
Oi M. Chan
Patrick S C Leung
Gary Wong
Ting Fan Leung
Title: Fish Allergenicity Ladder and Parvalbumin Epitopes for Predicting Clinical Cross-reactivity and Reintroduction
Description:
not-yet-known
not-yet-known
not-yet-known
unknown
Background: IgE-mediated fish allergy has long been considered
an umbrella term due to the high cross-reactivity of parvalbumin, the
major fish allergen.
Yet, clinical tolerance to certain fish highlights
allergenicity differences.
In this study, we sought to construct a fish
allergenicity ladder and identify fish parvalbumin epitopes to improve
the diagnosis of fish allergy.
Methods: Reported clinical
history and the serum-specific IgE (sIgE) responses of 200 fish allergic
patients were collected and analyzed, while the relative parvalbumin
content in different fish were measured for the construction of fish
allergenicity ladder.
Double-blind placebo-controlled food challenge
(DBPCFC) and open challenge against salmon, grass carp and grouper were
performed in 58 selected patients for validation of the ladder.
Epitope
mapping was performed by peptide array against parvalbumins of salmon
(both β-1 and β-2), cod, grouper, and grass carp with sera from fish
allergic (n=11), partial fish tolerant (n=12), and complete fish
tolerant (n=5) patients diagnosed based on oral food challenge outcome.
Results: The distribution pattern of clinical, sIgE and
molecular data and their strong positive correlation led to the
construction of a 4-step fish allergenicity ladder comprising: step 1 of
the least allergenic fishes (tuna, halibut, salmon), steps 2 (cod) and 3
(herring and grouper) of moderately allergenic fishes to step 4 of
highly allergenic fishes (catfish, grass carp and tilapia).
Epitope
mapping revealed one epitope from grouper parvalbumin (AA64-78) for
diagnosing general fish allergy and one epitopic region from salmon
parvalbumin (AA19-33) as biomarker of specific fish tolerance.
Only
epitope-specific IgE differentiated these patients but not sIgE to fish
extract or parvalbumin.
Conclusion: The fish ladder and
epitopes discovery can precisely differentiate fish-allergic and
tolerant subjects and guide fish reintroduction by stepping up the
ladder, which innovate fish allergy care in the next millennium.
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