Literature DB >> 12941484

Contrasting cellular responses in Schistosoma haematobium infected and exposed individuals from areas of high and low transmission in Zimbabwe.

T Mduluza1, P D Ndhlovu, N Midzi, J T Scott, F Mutapi, C Mary, P Couissinier-Paris, C M R Turner, S K Chandiwana, M E J Woolhouse, A J Dessein, P Hagan.   

Abstract

The study compared cytokine profiles of individuals from two areas with different transmission patterns for Schistosoma haematobium. One area was a high transmission (HT) while the other was a low transmission (LT) area for S. haematobium. Observations on cellular immune responses were made on stimulated peripheral blood mononuclear cells (PBMC), which were collected pre-treatment, then at 12 and 18 months post treatment. Stimulation was with schistosome worm and egg antigens and a mitogen, phaetohaemaglutinin (PHA). Observations were made on PBMC proliferation and the profiles of cytokine produced over a 5-day incubation period. The two distinct areas showed significant differences on both levels of proliferation and cytokine production for all the measured classes (IL-4, IL-5, IL-10 and IFN-gamma). PBMC from individuals from the LT area had high levels of proliferation but low cytokine production to both antigen stimulants while PBMC from individuals from the HT area showed low levels of proliferation but high cytokine production levels. Prior to treatment, individuals not excreting schistosome ova in the HT area had higher levels of proliferation to the stimulants, than the infected individuals. However, after treatment re-infected individuals showed high levels of proliferation. Before treatment, both infected and uninfected groups showed low and similar ratios, respectively, of IL-4:IFN-gamma, IL-5:IFN-gamma and IL-10:IFN-gamma, while IFN-gamma was high in the infected individuals. After treatment the non re-infected had higher levels of IL-4, IL-5 and IL-10, with the infected having high levels of IFN-gamma. Th1-like response dominated during infection with the Th2-like responses dominating post treatment and in uninfected individuals. The results indicated that the cytokine balance determines, in part, susceptibility or resistance to S. haematobium infection.

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Year:  2003        PMID: 12941484     DOI: 10.1016/s0165-2478(03)00088-9

Source DB:  PubMed          Journal:  Immunol Lett        ISSN: 0165-2478            Impact factor:   3.685


  8 in total

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2.  T regulatory cell levels decrease in people infected with Schistosoma mansoni on effective treatment.

Authors:  Kanji Watanabe; Pauline N M Mwinzi; Carla L Black; Erick M O Muok; Diana M S Karanja; W Evan Secor; Daniel G Colley
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3.  Human schistosome infection and allergic sensitisation.

Authors:  Nadine Rujeni; David W Taylor; Francisca Mutapi
Journal:  J Parasitol Res       Date:  2012-08-27

4.  Regulatory and activated T cells in human Schistosoma haematobium infections.

Authors:  Norman Nausch; Nicholas Midzi; Takafira Mduluza; Rick M Maizels; Francisca Mutapi
Journal:  PLoS One       Date:  2011-02-10       Impact factor: 3.240

5.  Circulating cytokine levels and antibody responses to human Schistosoma haematobium: IL-5 and IL-10 levels depend upon age and infection status.

Authors:  T Milner; L Reilly; N Nausch; N Midzi; T Mduluza; R Maizels; F Mutapi
Journal:  Parasite Immunol       Date:  2010 Nov-Dec       Impact factor: 2.280

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.  Down Regulation of the TCR Complex CD3ζ-Chain on CD3+ T Cells: A Potential Mechanism for Helminth-Mediated Immune Modulation.

Authors:  Laura J Appleby; Norman Nausch; Francesca Heard; Louise Erskine; Claire D Bourke; Nicholas Midzi; Takafira Mduluza; Judith E Allen; Francisca Mutapi
Journal:  Front Immunol       Date:  2015-02-18       Impact factor: 7.561

8.  Cytokine responses to Schistosoma haematobium in a Zimbabwean population: contrasting profiles for IFN-gamma, IL-4, IL-5 and IL-10 with age.

Authors:  Francisca Mutapi; Georgina Winborn; Nicholas Midzi; Matthew Taylor; Takafira Mduluza; Rick M Maizels
Journal:  BMC Infect Dis       Date:  2007-11-28       Impact factor: 3.090

  8 in total

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