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Regulatory and activated T cells in human Schistosoma haematobium infections.

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TLDR
The relationship between Tact proportions and schistosome infection intensity remained unchanged with age, however Treg proportions rose significantly with increasing infection in the younger age group, and in contrast Treg were negatively correlated to infection intensity in the older age group.
Abstract
Acquired immunity against helminths is characterised by a complex interplay between the effector Th1 and Th2 immune responses and it slowly manifests with age as a result of cumulative exposure to parasite antigens. Data from experimental models suggest that immunity is also influenced by regulatory T cells (Treg), but as yet studies on Treg in human schistosome infections are limited. This study investigated the relationship between schistosome infection intensity and the two cell populations regulatory T cells (Treg: CD4+(dim)CD25+(high)FOXP3+CD127low), and activated (Tact: CD4+CD25+FOXP3−) T cells in Zimbabweans exposed to Schistosoma haematobium parasites. Participants were partitioned into two age groups, young children (8–13 years) in whom schistosome infection levels were rising to peak and older people (14+ years) with declining infection levels. The relationship between Tact proportions and schistosome infection intensity remained unchanged with age. However Treg proportions rose significantly with increasing infection in the younger age group. In contrast Treg were negatively correlated to infection intensity in the older age group. The relative proportions of regulatory T cells differ significantly between young individuals in whom high infection is associated with an enhanced regulatory phenotype and older infected patients in whom the regulatory response is attenuated. This may influence or reflect different stages of the development of protective schistosome acquired immunity and immunopathogenesis.

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Journal ArticleDOI

Helminth Infections and Host Immune Regulation

TL;DR: There is much interest in whether helminth-associated immune regulation may ameliorate allergy and autoimmunity, with investigations in both laboratory models and human trials suggesting that parasites may protect against immunopathological syndromes.
Journal ArticleDOI

Immunology of human schistosomiasis.

TL;DR: There is a wealth of immunologic studies that have been carried out in experimental and human schistosomiasis that can be classified into three main areas: immunopathogenesis, resistance to reinfection and diagnostics, which contribute to the public health response to humanSchistosome infections.
Journal ArticleDOI

Susceptibility and immunity to helminth parasites

TL;DR: New studies identify innate lymphoid cells initiating immunity to helminths, and new immunoregulatory populations including macrophages, DCs and B cells are identified.
Journal ArticleDOI

T cells in helminth infection: the regulators and the regulated

TL;DR: Understanding of the multiple regulatory pathways within the T cell compartment is needed to counteract helminth-induced immunosuppression and induce long-term immunological memory, and the potential for reversing unresponsiveness through stimulatory signals or replacement by new responders is considered.
Journal ArticleDOI

Induction of regulatory cells by helminth parasites: exploitation for the treatment of inflammatory diseases

TL;DR: Experimental studies in mice have demonstrated that regulatory immune responses induced by helminth can suppress Th2 and Th1/Th17 responses that mediate allergy and autoimmunity, respectively, which has provided a rational explanation of the ‘hygiene hypothesis’.
References
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TL;DR: In this paper, the authors present a model for the analysis of variance in a single-classification and two-way and multiway analysis of Variance with the assumption of correlation.
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Biometry: The Principles and Practice of Statistics in Biological Research

TL;DR: In this paper, the authors present a model for the analysis of variance in a single-classification and two-way and multiway analysis of Variance with the assumption of correlation.
Journal ArticleDOI

Control of Regulatory T Cell Development by the Transcription Factor Foxp3

TL;DR: Foxp3, which encodes a transcription factor that is genetically defective in an autoimmune and inflammatory syndrome in humans and mice, is specifically expressed in naturally arising CD4+ regulatory T cells and retroviral gene transfer of Foxp3 converts naïve T cells toward a regulatory T cell phenotype similar to that of naturally occurring CD4+.
Journal ArticleDOI

Foxp3 programs the development and function of CD4 + CD25 + regulatory T cells

TL;DR: It is reported that the forkhead transcription factor Foxp3 is specifically expressed in CD4+CD25+ regulatory T cells and is required for their development and function and ectopic expression ofFoxp3 confers suppressor function on peripheral CD4-CD25− T cells.
Journal ArticleDOI

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TL;DR: The book aims to instill in students an ability to think through biological research problems in such a way as to grasp the essentials of the experimental or analytical setup to know which types of statistical tests to apply in a given case and to carry out the computations required.
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