Immune response of cattle immunized with a conjugate of the glycolipid glucose monomycolate and protein
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Date
Authors
Nguyen, Thi Kim Anh
Wieland, Willemien
Santema, Wiebren J.
Hoeboer, Jeroen
Van Eden, Willem
Rutten, Victor P.M.G.
Koets, Ad P.
Van Rhijn, Ildiko
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Abstract
Strong anti glycolipid IgG responses can occur in humans and animals, but contrary to anti protein responses and anti
glycoprotein responses, the exact mechanism of induction is unknown. We have previously shown that experimental
immunization with the glycolipid glucose monomycolate (GMM) causes the development of specific T cell responses, but
not of anti GMM antibodies. However, cattle naturally infected with Mycobacterium avium ssp. paratuberculosis produce high
levels of anti GMM IgG. In the present study, we tested whether vaccination with GMM conjugated to a protein mimics
natural infection in its capacity to induce the production of antibodies against GMM. Cattle were immunized (n = 5 per group)
with GMM conjugated to a protein, or GMM and protein non-conjugated and administered at contralateral locations, or
carrier only. Although immunization with the GMM-protein conjugate vaccine and the non-conjugated vaccine induced
protein specific antibody responses, GMM specific antibodies were not detected in either of the groups. In conclusion, the
generation of isotype-switched anti lipid antibodies appears to require more than providing peptide epitopes for T helper cells
to support glycolipid specific B cells in antibody production.
Description
Supplementary data associated with this article can be found as a separated attachment.
Keywords
Vaccines, Immunoglobulin, Mycobacterium tuberculosis, Conjugate vaccine, Cattle
Sustainable Development Goals
Citation
Nguyen, TKA, Wieland, W, Santema, W, Hoeboer, J, Van Eden, W, Rutten, VPMG, Koets, A & Van Rhijn, I 2011, 'Immune response of cattle immunized with a conjugate of the glycolipid glucose monomycolate and protein', Veterinary immunology and immunopathology, vol. 142, no. 3-4, pp. 265-270.
