Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1965 Dec;90(6):1675–1681. doi: 10.1128/jb.90.6.1675-1681.1965

Nonspecific Factors in Resistance of Mice to Experimental Tuberculosis

Guy P Youmans 1, Anne S Youmans 1
PMCID: PMC315877  PMID: 4955057

Abstract

Youmans, Guy P. (Northwestern University Medical School, Chicago, Ill.), and Anne S. Youmans. Nonspecific factors in resistance of mice to experimental tuberculosis. J. Bacteriol. 90:1675–1681. 1965.—In contrast to viable attenuated mycobacterial cells, Escherichia coli lipopolysaccharide (LPS) did not produce an acute pulmonary granulomatous response in mice, did not decrease the tolerance of mice to early subsequent intravenous injections of viable attenuated mycobacterial cells, nor did it increase susceptibility to tuberculous infection when injected simultaneously with virulent mycobacterial cells. When the injection of E. coli LPS was followed by the intravenous injection of virulent mycobacterial cells, there was a moderate increase in resistance to tuberculous infection which was maximal 7 to 14 days after the LPS injection. The degree of increased resistance to tuberculous infection was approximately the same as that produced by nearly maximal tolerated doses of heat-killed attenuated mycobacterial cells, and to that produced by a trichloroacetic acid extract of heat-killed attenuated mycobacterial cells. It is suggested that the major, if not entire, immunizing component of heat-killed attenuated mycobacterial cells resides in a heat-stable “nonspecific” component. A “multiple response” theory of immunity to tuberculosis is proposed.

Full text

PDF
1675

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CROWLE A. J. Immunizing constituents of the tubercle bacillus. Bacteriol Rev. 1958 Sep;22(3):183–203. doi: 10.1128/br.22.3.183-203.1958. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. DUBOS R. J., SCHAEDLER R. W. Effects of cellular constituents of mycobacteria on the resistance of mice to heterologous infections I. Protective effects. J Exp Med. 1957 Nov 1;106(5):703–717. doi: 10.1084/jem.106.5.703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. DUBOS R. ACQUIRED IMMUNITY TO TUBERCULOSIS. Am Rev Respir Dis. 1964 Oct;90:505–515. doi: 10.1164/arrd.1964.90.4.505. [DOI] [PubMed] [Google Scholar]
  4. ELBERG S. S., SCHNEIDER P., FONG J. Cross-immunity between Brucella melitensis and Mycobacterium tuberculosis; intracellular behavior of Brucella melitensis in monocytes from vaccinated animals. J Exp Med. 1957 Oct 1;106(4):545–554. doi: 10.1084/jem.106.4.545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. GIRARD G., GRUMBACH F. L'infection tuberculeuse de la souris entraine sa résistance à l'infection pesteuse expérimentale. C R Seances Soc Biol Fil. 1958;152(2):280–282. [PubMed] [Google Scholar]
  6. GLEDHILL A. W., REES R. J. Effect of a primary tuberculous infection on the resistance of male and female mice to Ectromelia. Nature. 1960 Aug 20;187:703–704. doi: 10.1038/187703b0. [DOI] [PubMed] [Google Scholar]
  7. HOWARD J. G., BIOZZI G., HALPERN B. N., STIFFEL C., MOUTON D. The effect of Mycobacterium tuberculosis (BCG) infection on the resistance of mice to bacterial endotoxin and Salmonella enteritidis infection. Br J Exp Pathol. 1959 Jun;40(3):281–290. [PMC free article] [PubMed] [Google Scholar]
  8. JENKIN C. R., ROWLEY D. BASIS FOR IMMUNITY TO TYPHOID IN MICE AND THE QUESTION OF "CELLULAR IMMUNITY". Bacteriol Rev. 1963 Dec;27:391–404. doi: 10.1128/br.27.4.391-404.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. LITCHFIELD J. T., Jr A method for rapid graphic solution of time-per cent effect curves. J Pharmacol Exp Ther. 1949 Dec;97(4):399-408, 3 tab. [PubMed] [Google Scholar]
  10. MILLMAN I. Nonspecific resistance to tuberculosis. Am Rev Respir Dis. 1961 May;83:668–675. doi: 10.1164/arrd.1961.83.5.668. [DOI] [PubMed] [Google Scholar]
  11. MYRVIK Q. N., LEAKE E. S., OSHIMA S. A study of macrophages and epitheloid-like cells from granulomatous (BCG-induced) lungs of rabbits. J Immunol. 1962 Nov;89:745–751. [PubMed] [Google Scholar]
  12. ROBSON J. M., SMITH J. T. Immunizing effects of a lipopolysaccharide in mice. Am Rev Respir Dis. 1961 Jul;84:100–102. doi: 10.1164/arrd.1961.84.1.100. [DOI] [PubMed] [Google Scholar]
  13. SCHAEDLER R. W., DUBOS R. J. Effects of cellular constituents of mycobacteria on the resistance of mice to heterologous infections. II. Enhancement of infection. J Exp Med. 1957 Nov 1;106(5):719–726. doi: 10.1084/jem.106.5.719. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. SUTER E., RAMSEIAR H. CELLULAR REACTIONS IN INFECTION. Adv Immunol. 1964;27:117–173. doi: 10.1016/s0065-2776(08)60707-5. [DOI] [PubMed] [Google Scholar]
  15. SUTER E., WHITE R. G. The response of the reticulo-endothelial system to the injection of the purified wax and the lipopolysaccharide of tubercle bacilli; a histologic and an immunologic study. Am Rev Tuberc. 1954 Nov;70(5):793–805. doi: 10.1164/art.1954.70.5.793. [DOI] [PubMed] [Google Scholar]
  16. WEISS D. W., BONHAG R. S., PARKS J. A. STUDIES ON THE HETEROLOGOUS IMMUNOGENICITY OF A MENTHANOL-INSOLUBLE FRACTION OF ATTENUATED TUBERCLE BACILLI (BCG). I. ANTIMICROBIAL PROTECTION. J Exp Med. 1964 Jan 1;119:53–70. doi: 10.1084/jem.119.1.53. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. WEISS D. W. Enhanced resistance of mice to infection with Pasteurella pestis following vaccination with fractions of phenol-killed tubercle bacilli. Nature. 1960 Jun 25;186:1060–1061. doi: 10.1038/1861060a0. [DOI] [PubMed] [Google Scholar]
  18. WILLIAMS C. A., Jr, DUBOS R. J. Studies on fractions of methanol extracts of tubercle bacilli. I. Fractions which increase resistance to infection. J Exp Med. 1959 Dec 1;110:981–1004. doi: 10.1084/jem.110.6.981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. YOUMANS A. S., YOUMANS G. P. FURTHER STUDIES ON A LABILE IMMUNOGENIC PARTICULATE SUBSTANCE ISOLATED FROM MYCOBACTERIUM TUBERCULOSIS. J Bacteriol. 1964 Feb;87:278–285. doi: 10.1128/jb.87.2.278-285.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. YOUMANS A. S., YOUMANS G. P. IMMUNOGENIC ACTIVITY OF A RIBOSOMAL FRACTION OBTAINED FROM MYCOBACTERIUM TUBERCULOSIS. J Bacteriol. 1965 May;89:1291–1298. doi: 10.1128/jb.89.5.1291-1298.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. YOUMANS A. S., YOUMANS G. P. NATURE OF THE LABILE IMMUNOGENIC SUBSTANCE IN THE PARTICULATE FRACTION ISOLATED FROM MYCOBACTERIUM TUBERCULOSIS. J Bacteriol. 1964 Oct;88:1030–1037. doi: 10.1128/jb.88.4.1030-1037.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. YOUMANS G. P., YOUMANS A. S. The measurement of the response of immunized mice to infection with Mycobacterium tuberculosis va. hominis. J Immunol. 1957 May;78(5):318–329. [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES