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Re-infection in human schistosomiasis mansoni: a prospective field study 18 months after praziquantel therapy.

作者信息

Zwingenberger K, Harms G, Poggensee U, Steiner A, Müller O, Feldmeier H

机构信息

Landesinstitut für Tropenmedizin, Berlin, F.R.G.

出版信息

Ann Trop Med Parasitol. 1990 Oct;84(5):457-65. doi: 10.1080/00034983.1990.11812495.

DOI:10.1080/00034983.1990.11812495
PMID:2124097
Abstract

Twenty-eight Zairean patients with Schistosoma mansoni infection were investigated and treated with praziquantel. Of these, 22 were re-examined 18 months later and 13 were found to be re-infected. Eighteen uninfected Zaireans were monitored concurrently to control for variations unrelated to schistosomiasis. Pathophysiological changes related to liver fibrosis were assessed by the determination of serum cholylglycine and procollagen-III-peptide. Circulating T-cell subsets were quantitated, and shedded T-cell antigens were measured in sera. In patients initially presenting with hepatomegaly, the biochemical indicators for egg-induced immunopathology became normal after therapy and remained normal even after re-infection, when the parasite load attained about 50% of the pretreatment level. Among T-cell phenotypes, CD4+ cells transiently increased by three months after treatment, but after 18 months the CD4/CD8 ratios both in patients then re-infected and in those not re-infected had reverted to the respective balances which had been observed at the start of the investigation. Both soluble CD8 antigen and interleukin 2 receptor in patients' sera were significantly elevated throughout the study period. The results indicate a dissociation of factors regulating fibrogenesis and immunomodulation after treatment and re-infected.

摘要

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