Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-29T01:15:41.234Z Has data issue: false hasContentIssue false

Immunoepidemiology of Ascaris lumbricoides: relationships between antibody specificities, exposure and infection in a human community

Published online by Cambridge University Press:  06 April 2009

M. R. Haswell-Elkins
Affiliation:
Tropical Health Program, Queensland Institute of Medical Research, Brisbane, Australia
H. Leonard
Affiliation:
Tropical Health Program, Queensland Institute of Medical Research, Brisbane, Australia
M. W. Kennedy
Affiliation:
Wellcome Laboratories for Experimental Parasitology, University of Glasgow, Scotland
D. B. Elkins
Affiliation:
Tropical Health Program, Queensland Institute of Medical Research, Brisbane, Australia
R. M. Maizels
Affiliation:
Department of Biology, Imperial College of Science, Technology and Medicine, London, U.K.

Summary

The serum antibody responses of 124 people naturally exposed to Ascaris lumbricoides infection were analysed by immunoprecipitation of radio-isotope labelled 3rd- and 4th-stage larval Ascaris suum excretory and secretory antigens (L3/4 ES). Profiles of antigens recognized were visualized by polyacrylamide gel electrophoresis (SDS–PAGE), and the band intensities of the 12 major precipitated antigens were individually scored. Most subjects were seropositive, but considerable variation was observed in the amount of total and individual ES antigens precipitated. The sex- and age-related profiles of antibody levels followed similar patterns to those of egg output. In addition, total antibody scores of individuals were closely correlated (r = 0.47–0.52) with their eggs per gram of faeces (e.p.g.) collected 4 months after blood samples were taken. These findings suggest that antibody levels against larval ES antigens reflect recent exposure and are consistent with the hypothesis that establishment of adult worms is proportional to the number of larvae that recently migrated through the lung.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1992

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Alexander, J. & Stimson, W. H. (1988). Sex hormones and the course of parasitic infection. Parasitology Today 4, 189–93.CrossRefGoogle Scholar
Anderson, R. M. (1986). The population dynamics and epidemiology of intestinal nematode infections. Transactions of the Royal Society of Tropical Medicine and Hygiene 80, 686–96.CrossRefGoogle ScholarPubMed
Bundy, D. A. P. (1988). Gender-dependent patterns of infection and disease. Parasitology Today 4, 186–9.CrossRefGoogle Scholar
Butterworth, A. E. & Hagan, P. (1987). Immunity in human schistosomiasis. Parasitology Today 3, 1116.CrossRefGoogle ScholarPubMed
Elkins, B., Haswell-Elkins, M. R. & Anderson, R. M. (1986). The epidemiology and control of intestinal helminths in the Pulicat Lake region of Southern India. I. Study design and pre- and post-treatment observations on Ascaris lumbricoides infection. Transactions of Royal Society of Tropical Medicine and Hygiene 80, 774–92.CrossRefGoogle Scholar
Elkins, D. B., Haswell-Elkins, M. R. & Anderson, R. M. (1988). The importance of host age and sex to patterns of reinfection with Ascaris lumbricoides following mass anthelmintic treatment of a South Indian fishing community. Parasitology 96, 171–84.CrossRefGoogle ScholarPubMed
Forrester, J. E., Scott, M. E., Bundy, D. A. P. & Golden, M. N. H. (1988). Clustering of Ascaris and Trichuris infections within households. Transactions of the Royal Society of Tropical Medicine and Hygiene 82, 282–8.CrossRefGoogle ScholarPubMed
Hagan, P., Blumenthal, U. J., Dunn, D., Simpson, A. J. G. & Wilkins, H. A. (1991). Human IgE, IgG4 and resistance to reinfection with Schistosoma haematobium. Nature, London 349, 243–5.CrossRefGoogle ScholarPubMed
Haswell-Elkins, M. R., Elkins, D. B. & Anderson, R. M. (1989 a). The influence of individual, social and household factors on the distribution of Ascaris lumbricoides within a community and implications for control strategies. Parasitology 98, 125–34.CrossRefGoogle ScholarPubMed
Haswell-Elkins, M. R., Kennedy, M. W., Maizels, R. M., Elkins, D. B. & Anderson, R. M. (1989 b). The antibody recognition profiles of humans naturally infected with Ascaris lumbricoides. Parasite Immunology 11, 615–21.CrossRefGoogle ScholarPubMed
Kennedy, M. W., Qureshi, F., Haswell-Elkins, M. R. & Elkins, D. B. (1987). Homology and heterology between the secreted antigens of the parasitic larval stages of Ascaris lumbricoides and Ascaris suum. Clinical and Experimental Immunology 61, 2030.Google Scholar
Markwell, M. A. K. & Fox, C. F. (1978). Surface-specific iodination of membrane proteins of viruses and eucaryotic cells using 1,3,4,6-tetrachloro-3α-, 6α- diphenylglycouril. Biochemistry 17, 4807–9.CrossRefGoogle Scholar
Sokal, R. R. & Rohlf, F. J. (1981). Biometry, 2nd Edn.New York: W. H. Freeman and Co.Google Scholar
Thein-Hlaing, Than-Saw, Htay-Htay-Aye, Myint-Lwin & Thein-Maung-Myint, (1984). Epidemiology and transmission dynamics of Ascaris lumbricoides in Opko Village, rural Burma. Transactions of the Royal Society of Tropical Medicine and Hygiene 78, 497504.CrossRefGoogle Scholar
Urban, J. F. & Romanwski, R. D. (1985). Ascaris suum: protective immunity in pigs immunized with products from eggs and larvae. Experimental Parasitology 60, 245–54.CrossRefGoogle ScholarPubMed
Wilkins, H. A., Blumenthal, U. J., Hagan, P., Hayes, R. J. & Tulloch, S. (1987). Resistance to reinfection after treatment of urinary schistosomiasis. Transactions of the Royal Society of Tropical Medicine and Hygiene 81, 2935.CrossRefGoogle ScholarPubMed