AJTMH HINARI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 14(2), 1965, pp. 239-253
Copyright © 1965 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cheever, A. W.
Right arrow Articles by Warren, K. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cheever, A. W.
Right arrow Articles by Warren, K. S.

Repeated Infection and Treatment of Mice with Schistosoma mansoni: Functional, Anatomic and Immunologic Observations

Allen W. Cheever, William B. Dewitt AND Kenneth S. Warren*
U. S. Department of Health, Education and Welfare, Public Health Service, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Laboratory of Parasitic Diseases, Bethesda, Maryland 20014

Mice were subjected to three courses of Schistosoma mansoni infection and subsequent stibophen treatment. Mice treated before or immediately after the onset of egg deposition showed little increase in portal pressure, liver size or spleen size. When treatment was withheld until four weeks after oviposition had begun, portal hypertension and hepatosplenomegaly appeared and were rapidly reversed following treatment.

No immunity was detected after challenge of previously infected and treated mice. Worm burdens and hepatic egg counts were similar to those in mice infected for the first time. Hepatic response to dead worms and to eggs was similar in simultaneously exposed animals experiencing their first and third infections.

Hepatic scars related to eggs and dead worms persisted in decreasing numbers until termination of the experiment more than a year after the last treatment. Dead worm lesions in the mice were focal, peripheral and predominantly intravascular. They did not appear to be histologically similar to the portal pipestem fibrosis seen in livers of humans with severe hepatosplenic schistosomiasis.


* Present address: Department of Preventive Medicine, School of Medicine, Western Reserve University, Cleveland 6, Ohio.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1965 by the American Society of Tropical Medicine and Hygiene.