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Streptococcal antibodies in patients with burn injuries

Published online by Cambridge University Press:  25 March 2010

J. P. Widdowson
Affiliation:
Division of Hospital Infection, Central Public Health Laboratory, Colindale Avenue, London NW9 5HT
P. J. Wormald
Affiliation:
Public Health Laboratory, Odstock Hospital, Salisbury
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Summary

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Serum samples from 14 patients whose burns had become infected with streptococci of groups A (11 patients), C (one patient) or G (two patients), and from 19 burned patients without bacteriological evidence of streptococcal infection were examined for anti-streptococcal antibodies. Tests were made for anti-streptolysin O (ASO), anti-hyaluronidase (AH), anti-deoxyribonuclease B (anti-DNAase B) and antibody against M-associated protein (MAP). Sera from the patients with streptococcal infections were also examined, when this was practicable, for ‘bactericidal’ (anti-M) antibody and for antibody against the opacity factor (OF) of the infecting serotype.

In patients infected with group A streptococci, the ASO response was generally poor, except in patients infected with strains of type T12/M12, and the AH response was rather similar, but most of the patients gave a rapid and vigorous anti-DNAase B response, except when the burn was small or colonization occurred very late. Antibody to the M and MAP antigens, and to OF (when the infecting strain formed this), was weak and transient, or absent, except in three of four patients infected with streptococci of type T12/M12.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1981

References

REFERENCES

Anthony, B. F., Perlman, L. V. & Wannamaker, L. W. (1967). Skin infections and acute nephritis in American Indian children. Pediatrics, Springfield 38, 263.CrossRefGoogle Scholar
Denny, F. W., Perry, W. D. & Wannamaker, L. W. (1957). Type-specific streptococcal antibody. Journal of Clinical Investigation 36, 1092.CrossRefGoogle ScholarPubMed
Dillon, H. C. & Derrick, C. W. (1979). Type-specific antibody response after pyoderma and acute glomerulonephritis: types 2 and 49. In Pathogenic Streptococci (ed. Parker, M. T.), p. 92. Reedbooks Ltd, Chertsey, Surrey.Google Scholar
Dillon, H. C. & Reeves, M. S. (1969). Streptococcal antibody titres in skin infection and acute glomerulonephritis. Pediatrics Research 3, 362.Google Scholar
Dudding, B. A. & Ayous, E. M. (1968). Persistence of streptococcal group A antibody in patients with rheumatic valvular disease. Journal of Experimental Medicine 128, 1081.CrossRefGoogle Scholar
Gooder, H. & Williams, R. E. O. (1961). Titration of antistreptolysin O. Association of Clinical Pathologists Broadsheet No. 34 (new series) London.Google Scholar
Griffith, F. (1934). The serological classification of Streptococcus pyogenes. Journal of Hygiene 34, 542.Google ScholarPubMed
Kaplan, E. L. & Wannamaker, L. W. (1976). Suppression of the antistreptolysin O response by cholesterol and by lipid extracts of rabbit skin. Journal of Experimental Medicine 144, 754.CrossRefGoogle ScholarPubMed
Lancefield, R. C. (1959). Persistence of type-specific antibodies in man following infection with group A streptococci. Journal of Experimental Medicine 110, 271.CrossRefGoogle ScholarPubMed
Maxted, W. R., Widdowson, J. P. & Fraser, C. A. M. (1973). Antibody to streptococcal opacity factor in human sera. Journal of Hygiene 71, 35.CrossRefGoogle ScholarPubMed
Maxted, W. R., Widdowson, J. P., Fraser, C. A. M., Ball, L. C. & Bassett, D. C. J. (1973). The use of the serum-opacity reaction in the tying of group A streptococci. Journal of Medical Microbiology 6, 83.CrossRefGoogle Scholar
Murphy, R. A. (1972). Improved antihyaluronidase test applicable to the microtitration technique. Applied Microbiology 23, 1170.CrossRefGoogle Scholar
Nelson, J., Ayoub, E. M. & Wannamaker, L. W. (1968). Streptococcal antideoxyribonuclease B: microtechnique determination. Journal of Laboratory and Clinical Medicine 71, 867.Google Scholar
Potter, E. V., Ortiz, J. S., Sharratt, A. R., Burt, E. G., Bray, J. P., Finklea, J. F., Poon-King, T. & Earle, D. P. (1971). Changing types of nephritogenic streptococci in Trinidad. Journal of Clinical Investigation 50, 1197.CrossRefGoogle ScholarPubMed
Rotta, J., Krause, R. M., Lancefield, R. C., Everly, W. & Lackland, H. (1971). New approaches for the laboratory recognition of M types of group A streptococci. Journal of Experimental Medicine 134, 1298.CrossRefGoogle ScholarPubMed
Widdowson, J. P., Maxted, W. R. & Pinney, A. M. (1971). An M-associated protein antigen (MAP) of group A streptococci. Journal of Hygiene 69, 553.Google ScholarPubMed
Widdowson, J. P., Maxted, W. R., Notley, C. M. & Pinney, A. M. (1974). The antibody response in man to infection with different serotypee of group A streptococci. Journal of Medical Microbiology 1, 483.CrossRefGoogle Scholar
Wormald, P. J. (1970). The effect of a changed environment on bacterial colonization rates in an established burns centre. Journal of Hygiene 68, 633.Google Scholar