Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1980 Jan;27(1):81-6.
doi: 10.1128/iai.27.1.81-86.1980.

Influence of route of administration on immediate and extended protection in rats immunized with Escherichia coli heart-labile enterotoxin

Influence of route of administration on immediate and extended protection in rats immunized with Escherichia coli heart-labile enterotoxin

F A Klipstein et al. Infect Immun. 1980 Jan.

Abstract

The effect of route of administration, dosage, and number of boosts employed during immunization with the polymyxin-release form of Escherichia coli heat-labile (LT) enterotoxin on the degree and duration of protection afforded was evaluated in rats which were challenged by the ligated loop technique. Increasing the boosting dosage by fivefold from 50 to 250 mug resulted in a marked increase in protection against challenge with toxin in rats immunized either just by the parenteral route (i.p./i.p.) or by a parenteral prime, followed by peroral boosts (i.p./p.o.) in rats pretreated with cimetidine to ablate gastric secretions; such was not the case, however, even with a 50-fold increase in dosage in rats immunized just by the peroral route (p.o./p.o.). Four weekly peroral boosts were required to achieve the strongest degree of protection. Increasing the boosting dosage also increased the degree of protection against challenge with viable LT(+)/ST(-) and LT(+)/ST(+) strains (ST indicates heat-stable enterotoxin) in rats immunized by the i.p./p.o., but not by the i.p./i.p., route; no protection was evident against an LT(-)/ST(+) strain. Protection was lost within 3 weeks after immunization in rats immunized by the i.p./i.p. route. In contrast, protection was extended over the 3-month observation period in those immunized by the i.p./p.o. route; the degree of protection was enhanced in rats which received an additional boost at 2 months. These observations establish the fact that immunization with LT is similar to that with cholera toxin in that arousal of the local immune intestinal response by means of peroral immunization provides maximal extended protection.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Clin Microbiol. 1977 Jun;5(6):570-2 - PubMed
    1. Infect Immun. 1979 Jun;24(3):774-9 - PubMed
    1. Nature. 1979 Feb 1;277(5695):406-7 - PubMed
    1. Infect Immun. 1979 Apr;24(1):19-23 - PubMed
    1. Infect Immun. 1974 Nov;10(5):1010-7 - PubMed

Publication types