Abstract
Mice immunized with typhoid-paratyphoid vaccine USP were found to be protected when challenged with serological groups A, B, and C of Neisseria meningitidis. Mice immunized with this vaccine both 14 and 7 days prior to challenge were protected against mean lethal doses (LD50) of 5,220 and 1,151 of groups A and B, respectively, and in two separate experiments they were protected against 3,568 and 268 LD50 of group C. Mice immunized four or more times on successive days prior to challenge were also protected. They demonstrated tolerance and survived a much larger LD50 challenge than mice immunized by any other immunization schedule. Mice immunized once or twice anytime within 7 days prior to challenge were not protected and thus failed to exhibit nonspecific resistance. Serum antibody probably was responsible for the protection afforded mice immunized 14 and 7 days prior to challenge. However, this was not demonstrated conclusively.
Full text
PDF




Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Berger F. M., Fukui G. M., Ludwig B. J., Rosselet J. P. Increase of nonspecific resistance to infection by protodyne, a protein component derived from bacterial protoplasm. Proc Soc Exp Biol Med. 1968 Feb;127(2):556–559. doi: 10.3181/00379727-127-32739. [DOI] [PubMed] [Google Scholar]
- CORDOBA F., HEIDELBERGER M. Cross-reactions of antityphoid and antiparatyphoid B horse sera with various polysaccharides. J Exp Med. 1956 Sep 1;104(3):375–382. doi: 10.1084/jem.104.3.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Devine L. F., Hagerman C. R. Relationship of Serogroups of Neisseria meningitidis I. Microagglutination, Gel Diffusion, and Slide Agglutination Studies of Meningococcal Antisera Before and After Absorption with RAS-10 Strain of Meningococci. Infect Immun. 1970 Mar;1(3):226–231. doi: 10.1128/iai.1.3.226-231.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LANDY M., PILLEMER L. Increased resistance to infection and accompanying alteration in properidin levels following administration of bacterial lipopolysaccharides. J Exp Med. 1956 Sep 1;104(3):383–409. doi: 10.1084/jem.104.3.383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LUDERITZ O., WESTPHAL O., STAUB A. M., LE MINOR L. Preparation and immunological properties of an artificial antigen with colitose (3-deoxy-1-fucose) as the determinant group. Nature. 1960 Nov 12;188:556–558. doi: 10.1038/188556a0. [DOI] [PubMed] [Google Scholar]
- Lüderitz O., Staub A. M., Westphal O. Immunochemistry of O and R antigens of Salmonella and related Enterobacteriaceae. Bacteriol Rev. 1966 Mar;30(1):192–255. doi: 10.1128/br.30.1.192-255.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McCabe W. R. Immunization with R mutants of S. Minnesota. I. Protection against challenge with heterologous gram-negative bacilli. J Immunol. 1972 Mar;108(3):601–610. [PubMed] [Google Scholar]
- Nowotny A. Molecular aspects of endotoxic reactions. Bacteriol Rev. 1969 Mar;33(1):72–98. doi: 10.1128/br.33.1.72-98.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROWLEY D. Rapidly induced changes in the level of non-specific immunity in laboratory animals. Br J Exp Pathol. 1956 Jun;37(3):223–234. [PMC free article] [PubMed] [Google Scholar]
- ROWLEY D. Stimulation of natural immunity to Escherichia coli infection: observations on mice. Lancet. 1955 Jan 29;268(6857):232–234. doi: 10.1016/s0140-6736(55)90163-x. [DOI] [PubMed] [Google Scholar]
- Rosselet J. P., Murphy S. G., Adamski R. J., Fletcher M. J., Ludwig B. J. Endotoxin-free biologically active component of Escherichia coli. J Bacteriol. 1969 May;98(2):434–436. doi: 10.1128/jb.98.2.434-436.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stone S. H. Method for Obtaining Venous Blood from the Orbital Sinus of the Rat or Mouse. Science. 1954 Jan 15;119(3081):100–100. doi: 10.1126/science.119.3081.100. [DOI] [PubMed] [Google Scholar]
