Literature DB >> 12791104

Chemotherapy-induced, age-related changes in antischistosome antibody responses.

Francisca Mutapi1, Paul Hagan, Mark E J Woolhouse, Takafira Mduluza, Patricia D Ndhlovu.   

Abstract

Humoral responses directed against Schistosoma mansoni soluble egg antigen were studied in Zimbabwean children before and after treatment with either praziquantel (PZQ) or oxamniquine (OXAM). Treated children showed a significant increase in the proportion producing IgE and IgG3 and in mean levels of IgE, IgM, IgG3 six weeks post-treatment. At 18 weeks post-treatment, the proportion of treated children producing IgA, IgE, and IgG3 increased while the proportion producing IgG1 and IgG4 decreased. Mean levels of IgA, IgE, and IgG3 were higher than pre-treatment levels while levels of IgG1, IgG4 and IgM were lower. Statistical analyses showed that the magnitude of change in levels of IgE, IgM and IgG3 at 6 weeks post-treatment and of IgE, IgG3 and IgG4 at 18 weeks post-treatment was significantly greater in treated compared to untreated children, and there were no significant differences in immune responses between children treated with praziquantel and those treated with oxamniquine. The magnitude of change in IgE at 6 and 18 weeks, IgM at 6 weeks and IgG3 at 18 weeks post-treatment were significantly associated with age in treated but not in untreated children, with the change being greater in younger children. This suggests that treatment induced a change in the age-antibody relationship for these isotypes, and that the age-antibody relationship is not robust to chemotherapy. Pre-treatment infection levels were significantly associated (positive correlation) with the magnitude of change for IgE and IgG3 at 18 weeks post-treatment. Taken together, these results indicate that the age-antibody relationship observed in these children is due, at least in part, to cumulative host experience of parasite antigens and not host age alone.

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Year:  2003        PMID: 12791104     DOI: 10.1046/j.1365-3024.2003.00610.x

Source DB:  PubMed          Journal:  Parasite Immunol        ISSN: 0141-9838            Impact factor:   2.280


  12 in total

1.  Increases in levels of schistosome-specific immunoglobulin E and CD23(+) B cells in a cohort of Kenyan children undergoing repeated treatment and reinfection with Schistosoma mansoni.

Authors:  Carla L Black; Erick M O Muok; Pauline N M Mwinzi; Jennifer M Carter; Diana M S Karanja; W Evan Secor; Daniel G Colley
Journal:  J Infect Dis       Date:  2010-08-15       Impact factor: 5.226

2.  Development of a specimen-sparing multichannel bead assay to detect antiparasite IgG4 for the diagnosis of Schistosoma and Wuchereria infections on the coast of Kenya.

Authors:  Adam S DuVall; Jessica K Fairley; Laura Sutherland; Amaya L Bustinduy; Peter L Mungai; Eric M Muchiri; Indu Malhotra; Uriel Kitron; Charles H King
Journal:  Am J Trop Med Hyg       Date:  2014-02-10       Impact factor: 2.345

3.  Schistosoma haematobium infection levels determine the effect of praziquantel treatment on anti-schistosome and anti-mite antibodies.

Authors:  N Rujeni; N Nausch; N Midzi; T Mduluza; D W Taylor; F Mutapi
Journal:  Parasite Immunol       Date:  2012-06       Impact factor: 2.280

4.  A multicentre randomized controlled trial of the efficacy and safety of single-dose praziquantel at 40 mg/kg vs. 60 mg/kg for treating intestinal schistosomiasis in the Philippines, Mauritania, Tanzania and Brazil.

Authors:  Piero L Olliaro; Michel T Vaillant; Vincente J Belizario; Nicholas J S Lwambo; Mohamed Ouldabdallahi; Otavio S Pieri; Maria L Amarillo; Godfrey M Kaatano; Mamadou Diaw; Analucia C Domingues; Tereza C Favre; Olivier Lapujade; Fabiana Alves; Lester Chitsulo
Journal:  PLoS Negl Trop Dis       Date:  2011-06-14

Review 5.  Acquired immune heterogeneity and its sources in human helminth infection.

Authors:  C D Bourke; R M Maizels; F Mutapi
Journal:  Parasitology       Date:  2010-10-15       Impact factor: 3.234

6.  Group 2 innate lymphoid cell proportions are diminished in young helminth infected children and restored by curative anti-helminthic treatment.

Authors:  Norman Nausch; Laura J Appleby; Alexandra M Sparks; Nicholas Midzi; Takafira Mduluza; Francisca Mutapi
Journal:  PLoS Negl Trop Dis       Date:  2015-03-23

7.  Use of humanised rat basophilic leukaemia cell line RS-ATL8 for the assessment of allergenicity of Schistosoma mansoni proteins.

Authors:  Daniel Wan; Fernanda Ludolf; Daniel G W Alanine; Owen Stretton; Eman Ali Ali; Nafal Al-Barwary; Xiaowei Wang; Michael J Doenhoff; Adriano Mari; Colin M Fitzsimmons; David W Dunne; Ryosuke Nakamura; Guilherme C Oliveira; Marcos J C Alcocer; Franco H Falcone
Journal:  PLoS Negl Trop Dis       Date:  2014-09-25

8.  Comparing parasitological vs serological determination of Schistosoma haematobium infection prevalence in preschool and primary school-aged children: implications for control programmes.

Authors:  Welcome M Wami; Norman Nausch; Katharina Bauer; Nicholas Midzi; Reggis Gwisai; Peter Simmonds; Takafira Mduluza; Mark Woolhouse; Francisca Mutapi
Journal:  Parasitology       Date:  2014-03-28       Impact factor: 3.234

9.  Immunological consequences of antihelminthic treatment in preschool children exposed to urogenital schistosome infection.

Authors:  Nadine Rujeni; Norman Nausch; Nicholas Midzi; Graeme J Cowan; Richard Burchmore; David R Cavanagh; David W Taylor; Takafira Mduluza; Francisca Mutapi
Journal:  J Trop Med       Date:  2013-06-05

10.  New Allergens of Relevance in Tropical Regions: The Impact of Ascaris lumbricoides Infections.

Authors:  Luis Caraballo; Nathalie Acevedo
Journal:  World Allergy Organ J       Date:  2011-05       Impact factor: 4.084

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