Abstract

The same mechanisms that enable host defense against helminths also drive allergic inflammation. This suggests that pathomechanisms of allergic diseases represent evolutionary old responses against helminth parasites and that studying antihelminth immunity may provide insights into pathomechanisms of asthma. However, helminths have developed an intricate array of immunoregulatory mechanisms to modulate type 2 immune mechanisms. This has led to the hypothesis that the lack of helminth infection may contribute to the rise in allergic sensitization in modern societies. Indeed, the anti-inflammatory potential of helminth (worm) parasites and their products in allergy and asthma has been recognized for decades. As helminth infections bring about multiple undesired effects including an increased susceptibility to other infections, intended helminth infection is not a feasible approach to broadly prevent or treat allergic asthma. Thus, the development of new helminth-based biopharmaceutics may represent a safer approach of harnessing type 2–suppressive effects of helminths. However, progress regarding the mechanisms and molecules that are employed by helminths to modulate allergic inflammation has been relatively recent. The scavenging of alarmins and the modulation of lipid mediator pathways and macrophage function by helminth proteins have been identified as important immunoregulatory mechanisms targeting innate immunity in asthma and allergy. In addition, by regulating the activation of dendritic cells and by promoting regulatory T-cell responses, helminth proteins can counterregulate the adaptive T helper 2 cell response that drives allergic inflammation. Despite these insights, important open questions remain to be addressed before helminth molecules can be used for the prevention and treatment of asthma and other allergic diseases.

Highlights

  • Helminth infections affect about 2 billion people worldwide, and children in developing countries are susceptible [1]

  • Infection with the intestinal parasite Strongyloides stercoralis was associated with an increased risk of asthma and its exacerbation [21, 30, 31] and Toxocara species infection resulted in increased allergy and asthma prevalence in children, which positively correlated with serum IgE levels [32,33,34]

  • Helminths have unique immune regulatory potential, and understanding the complex array of immune responses triggered by these parasites may be instrumental for the diagnosis, prevention, and treatment of type 2 inflammatory diseases, such as allergic asthma

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Summary

INTRODUCTION

Helminth infections affect about 2 billion people worldwide, and children in developing countries are susceptible [1]. Helminth infections can be asymptomatic or induce pathology in the host, with malnutrition, anemia, educational loss, and cognitive deficits as major consequences [2,3,4]. Helminths usually infest their host as tissue-migratory larvae, which establish niches in the lung, skin, liver, or intestine, where they develop, mate, and release new infectious offspring

Allergy Modulation by Helminth Molecules
EPIDEMIOLOGICAL EVIDENCE FOR PROTECTIVE ROLES OF HELMINTHS IN ALLERGY AND ASTHMA
IMMUNOMODULATION OF ASTHMA AND ALLERGIC DISEASES BY HELMINTH MOLECULES
DISCUSSION
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