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Protection in lambs vaccinated with Haemonchus contortus antigens is age related, and correlates with IgE rather than IgG1 antibody
Author(s) -
Kooyman,
Schallig,
van Leeuwen,
Mackellar,
Huntley,
Cornelissen,
Vervelde
Publication year - 2000
Publication title -
parasite immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.795
H-Index - 75
eISSN - 1365-3024
pISSN - 0141-9838
DOI - 10.1046/j.1365-3024.2000.00265.x
Subject(s) - biology , immunology , haemonchus contortus , vaccination , immunoglobulin e , eosinophilia , antibody , physiology , helminths
Protection by vaccination with excretory–secretory products (ES) from Haemonchus contortus , containing predominantly proteins of 15 and 24 kDa, against an experimental challenge infection depends on the age of the sheep. Vaccinated sheep 9, 6 or 3 months of age were protected for 83%, 77% and −34%, respectively. There was a significant difference in ES‐specific serum IgE response but not in IgG1 response, after the last vaccination between the different age groups. In the protected 9‐month‐old animals, there was an increase up to 18 times the prevaccination levels, while the increase in the unprotected 3‐month‐old animals was at most 1.4 times. The 6‐month‐old animals showed an intermediate increase of approximately six times the prevaccination level. There was no correlation within the 9‐month‐old sheep between ES‐specific IgE levels and protection, measured as worm burden. However, when the different age groups were combined, there was a positive correlation (r = 0.38) between protection and ES‐specific IgE levels 1 week after the vaccination. At the end of the experiment, peripheral blood eosinophils and mast cell counts in abomasal tissue were also significantly higher in the vaccinated and challenged 9‐month‐old sheep than in the vaccinated and challenged 3‐month‐old or than in the 9‐month‐old sheep with challenge, but without vaccination. Increased serum IgE levels, eosinophilia and mucosal mast cell hyperplasia are the hallmarks of a Th2 response and were all demonstrated in protected, older sheep, but not in unprotected, younger sheep .