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Infection and Immunity, May 2001, p. 3476-3482, Vol. 69, No. 5
Department of Pathology and Molecular
Medicine, McMaster University, Hamilton, Ontario, Canada L8N
3Z5,1 and Department of Pathology and
Microbiology, University of Bristol, Bristol, United
Kingdom2
Received 18 October 2000/Returned for modification 15 December
2000/Accepted 16 February 2001
Although cholera toxin (Ctx) and Escherichia coli
heat-labile enterotoxin (Etx) are known to be potent mucosal adjuvants, it remains controversial whether the adjuvanticity of the holotoxins extends to their nontoxic, receptor-binding B subunits. Here, we have
systematically evaluated the comparative adjuvant properties of highly
purified recombinant EtxB and CtxB. EtxB was found to be a more potent
adjuvant than CtxB, stimulating responses to hen egg lysozyme when the
two were coadministered to mice intranasally, as assessed by enhanced
serum and secretory antibody titers as well as by stimulation of
lymphocyte proliferation in spleen and draining lymph nodes. These
results indicate that, although structurally very similar, EtxB and
CtxB have strikingly different immunostimulatory properties and should
not be considered equivalent as prospective vaccine adjuvants.
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.5.3476-3482.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Escherichia coli Heat-Labile Enterotoxin
B Subunit Is a More Potent Mucosal Adjuvant than Its Closely
Related Homologue, the B Subunit of Cholera Toxin
*
Corresponding author. Present address: Department of
Medical Biophysics, Ontario Cancer Institute, 610 University Ave., Room 8-318, Toronto, Ontario, Canada M5G 2M9. Phone: (416) 946-4501, ext.
5471. Fax: (416) 946-2086. E-mail:
dmillar{at}uhnres.utoronto.ca.
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