Skip to main content

Part of the book series: Current Topics in Infectious Disease ((CTID))

Abstract

Very little is known about the mechanisms of host defense in intravascular infections. Considerable emphasis is put on the ineffectiveness of conventional mechanisms: the lack of a lytic effect of antibody and complement on the gram-positive cocci responsible for the vast majority of infections and the inability of polymorphonuclear leukocytes (PMN) to penetrate the fibrin barrier surrounding developing bacterial colonies. These two factors, in addition to the diminished metabolic activity of colonies located deep in the vegetations (with the consequence that they would be theoretically less susceptible to the action of antibiotics, such as penicillin), serve as the theoretical basis for the empirical clinical reality that it takes long-term treatment with bactericidal antibiotics to cure intravascular infections.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Francioli, P., Freedman, L. R.: Streptococcal infection of endocardial and other intravascular vegetations in rabbits: Natural history and effect of dexamethasone. Infect. Immun. 24: 483–491, 1979.

    PubMed  CAS  Google Scholar 

  2. Perlman, B. B., Freedman, L. R.: Experimental endocarditis. III. Natural history of catheter induced endocarditis after catheter removal. Yale J. Biol. Med. 44: 214–223, 1971.

    PubMed  CAS  Google Scholar 

  3. Libman, E., Friedberg, C. K.: Subacute Bacterial Endocarditis. Oxford University Press, New York, 1971, 108 pages.

    Google Scholar 

  4. Carrizosa, J., Tanphaichitra, D., Levison, M. E.: Experimental Bacteroides fragilis endocarditis in rabbits. Infect. Immun 15 (3): 871–873, 1977.

    PubMed  CAS  Google Scholar 

  5. Rodbard, S.: Blood velocity and endocarditis. Circulation 27: 18–28, 1963.

    PubMed  CAS  Google Scholar 

  6. Messner, R. P., Laxdal, T., Quie, P. G., Williams, R. C., Jr.: Serum opsonin, bacteria, and polymorphonuclear leukocyte interactions in subacute bacterial endocarditis. J. Clin. Invest. 47:1109–1120, 1968.

    Google Scholar 

  7. Repine, J. E., Clawson, C. C., Burchell, H. B., White, J. G.: Reversible neutrophil defect in patients with bacterial endocarditis. J. Lab. Clin. Med 88 (5): 780–787, 1976.

    PubMed  CAS  Google Scholar 

  8. Freedman, L. R., Valone, J.: Experimental endocarditis. Prog. Cardiovasc. Diseases 22:169–180 1979.

    Google Scholar 

  9. Durack, D. T.: Experimental bacterial endocarditis. IV. Structure and evolution of very early lesions. J. Pathol 115: 81–89, 1975.

    Article  PubMed  CAS  Google Scholar 

  10. Yersin, B., Glauser, M., Freedman, L. R.: Unpublished observations.

    Google Scholar 

  11. Riba, A. L., Thakur, M. T., Gottschalk, A., Andriole, V. T., Zaret, B. L.: Imaging experimental infective endocarditis with indium-111-labeled blood cellular components. Circulation 59 (2): 336–343, 1979.

    PubMed  CAS  Google Scholar 

  12. Moore, W. S.: Experimental studies relating to sepsis in prosthetic vascular grafting, in: Infections of Prosthetic Heart Valves and Vascular Grafts. Duma, R. J., ed. University Park Press, Baltimore, pp. 267–285, 1977.

    Google Scholar 

  13. Pelletier, L. L., Petersdorf, R. G., Nielson, K.: Chemotherapy or experimental streptococcal endocarditis. V. Effect of duration of infection and retained intracardiac catheter on response to treatment. J. Lab. Clin. Med. 87 (4): 692–702, 1976.

    PubMed  Google Scholar 

  14. Heraief, E., Glauser, M., Freedman, L. R.: Vancomycin prophylaxis of streptococcal endocarditis in rats, in: Current Chemotherapy and Infectious Disease (Proceedings of the 11th International Congress of Chemotherapy and 19th Interscience Conference on Antimicrobial Agents and Chemotherapy), American Society for Microbiology, Washington, D. C., pp. 911–913, 1980.

    Google Scholar 

  15. Galgiani, J. N., Stevens, D. A.: Fungal endocarditis: Need for guidelines in evaluating therapy-experience with two patients previously reported. J. Thorac. Cardiovasc. Surg 73 (2): 293–296, 1977.

    PubMed  CAS  Google Scholar 

  16. McDermott, W.: Inapparent infection-Relation of latent and dormant infections to microbial persistence. Public Health Rep. 74 (6): 485–499, 1959.

    Article  PubMed  CAS  Google Scholar 

  17. Durack, D. T., Beeson, P. B.: Experimental bacterial endocarditis. II. Survival of bacteria in endocardial vegetations. Br. J. Exp. Pathol 53: 50–53, 1972.

    PubMed  CAS  Google Scholar 

  18. Durack, D. T., Beeson, P. B.: Protective role of complement in experimental Escherichia coli endocarditis. Infect. Immun. 16(1):213–217 1977.

    Google Scholar 

  19. Archer, G., Fekety, F. R., Jr.: Experimental endocarditis due to Pseudomones aeruginosa. I. Description of a model. J. Infect. Dis 134: 1–7, 1976.

    Article  PubMed  CAS  Google Scholar 

  20. Kaspar, R. L., Drutz, D. J.: Perihepatitis and hepatitis as complications of experimental endocarditis due to Neisseria gonorrhoeae in the rabbit. J . Infect. Dis. 136 (1): 37–42, 1977.

    Article  PubMed  CAS  Google Scholar 

  21. Alexander, W. J., Curtiss, R., HI, Bradac, J. A., Cobbs, C. G.: Rifampin modifies serum susceptibility of E. coli and its virulence in rabbit endocarditis model (abstract). Clin. Res. 26 (1): 26A, 1978.

    Google Scholar 

  22. Swift, H. F.: The heart in infection. Am. Heart J. 3 (6): 629–648, 1928.

    Article  Google Scholar 

  23. Wright, H. D.: The production of experimental endocarditis with pneumococci and streptococci in immunised animals. J. Pathol. Bacteriol 29: 5–11, 1926.

    Article  Google Scholar 

  24. Durack, D. T., Gilliland, B. C., Petersdorf, R. G.: Effect of immunization on susceptibility to experimental Streptococcus mutans and Streptococcus sanguis endocarditis. Infect. Immun

    Google Scholar 

  25. Scheid, W. M., Thomas, J. H., Sande, M. A.: Influence of preformed antibody on experimental Streptococcus sanguis endocarditis. Infect. Immun. 25: 781–785, 1979.

    Google Scholar 

  26. Thorig, L., Thompson, J., Eulderink, F., van Furth, R.: The role of host factors in the pathogenesis of bacterial endocarditis. Neth. J. Med. 22 (5): 174–175, 1979.

    Google Scholar 

  27. Hinthom, D. R., Mitchell, G. W., Liu, C.: Importance of preformed antibody in pathogenesis of experimental endocarditis. 18th Interscience Conference on Antimicrobial Agents and Chemotherapy. Abstract 279, 1978.

    Google Scholar 

  28. Archer, G. L., Johnston, J. L.: Effect of type-specific active immunization on the development and progression of experimental Pseudomonas aeruginosa endocarditis. Infect. Immun. 24 (1): 167–173, 1979.

    PubMed  CAS  Google Scholar 

  29. Arnold, S. B., Valone, J. A., Askenase, P. W., Kashgarian, M., Freedman, L. R.: Diffuse glomerulonephritis in rabbits with Streptococcus viridans endocarditis. Lab. Invest. 32 (6): 681–689, 1975.

    PubMed  CAS  Google Scholar 

  30. Thorig, L., Daha, M. R., Eulderink, F., Kooy-Bauer, W. C., Thompson, J.: Experimental Streptococcus sanguis endocarditis: Immune complexes and renal involvement. Clin. Exp. Immunol. 40: 469–477, 1980.

    PubMed  CAS  Google Scholar 

  31. Bryan, C. S., Marney, S. R., Alford, R. H., Bryant, R. E.: Gram negative bacillary endocarditis. Am. J. Med 58: 209–215, 1975.

    Article  PubMed  CAS  Google Scholar 

  32. West, T., Cantey, J. R., West, M., Yoakum, S., Burdash, N.: Encapsulation as a virulence factor in experimental coagulase-negative staphylococcal endocarditis. Clin. Res 28: 382A, 1980.

    Google Scholar 

  33. McGowan, D. A., Gillett, R.: Scanning electron microscopic observations of the surface of the initial lesion in experimental streptococcal endocarditis in the rabbit. Br. J. Exp. Pathol. 61: 164–171, 1980.

    PubMed  CAS  Google Scholar 

  34. Pruul, H., Wetherall, B. L., McDonald, P. J.: Activity of human leucocyte granule extract on antibiotic-damaged bacteria. 20th Interscience Conference on Antimicrobial Agents and Chemotherapy, Sept. 1980, Abstract 732.

    Google Scholar 

  35. Gerding, D. M., Peterson, L. R., Moore, B. M., Bean, B.: Effect of local polymorphonuclear leucocytes (PMN) on resolution of S. aureus abscesses treated with cephalothin (K). 20th Interscience Conference on Antimicrobial Agents and Chemotherapy, Sept. 1980, Abstract 685.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

Copyright information

© 1982 Plenum Publishing Corporation

About this chapter

Cite this chapter

Freedman, L.R. (1982). Host Defense Mechanisms. In: Infective Endocarditis and Other Intravascular Infections. Current Topics in Infectious Disease. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-8208-9_7

Download citation

  • DOI: https://doi.org/10.1007/978-1-4684-8208-9_7

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4684-8210-2

  • Online ISBN: 978-1-4684-8208-9

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics