» Articles » PMID: 20150967

Immunity Against Helminths: Interactions with the Host and the Intercurrent Infections

Overview
Specialty Biology
Date 2010 Feb 13
PMID 20150967
Citations 71
Authors
Affiliations
Soon will be listed here.
Abstract

Helminth parasites are of considerable medical and economic importance. Studies of the immune response against helminths are of great interest in understanding interactions between the host immune system and parasites. Effector immune mechanisms against tissue-dwelling helminths and helminths localized in the lumen of organs, and their regulation, are reviewed. Helminth infections are characterized by an association of Th2-like and Treg responses. Worms are able to persist in the host and are mainly responsible for chronic infection despite a strong immune response developed by the parasitized host. Two types of protection against the parasite, namely, premune and partial immunities, have been described. Immune responses against helminths can also participate in pathogenesis. Th2/Treg-like immunomodulation allows the survival of both host and parasite by controlling immunopathologic disorders and parasite persistence. Consequences of the modified Th2-like responses on co-infection, vaccination, and inflammatory diseases are discussed.

Citing Articles

Immune modulation of buffalo peripheral blood mononuclear cells by two asparaginyl endopeptidases from Fasciola gigantica.

Wu D, Guo Y, Zou Y, Tang X, Zhang W, Di W Parasit Vectors. 2024; 17(1):516.

PMID: 39696651 PMC: 11656647. DOI: 10.1186/s13071-024-06570-5.


Exposure to common infections may shape basal immunity and potentially HIV-1 acquisition amongst a high-risk population in Coastal Kenya.

Fwambah L, Andisi C, Streatfield C, Bromell R, Hare J, Esbjornsson J Front Immunol. 2024; 14:1283559.

PMID: 38274822 PMC: 10808675. DOI: 10.3389/fimmu.2023.1283559.


Impact of anthropogenous environmental factors on the marine ecosystem of trophically transmitted helminths and hosting seabirds: Focus on North Atlantic, North Sea, Baltic and the Arctic seas.

Schwantes U Helminthologia. 2024; 60(4):300-326.

PMID: 38222492 PMC: 10787638. DOI: 10.2478/helm-2023-0034.


Enhanced protective immunity against Baylisascaris schroederi infection in mice through a multi-antigen cocktail vaccine approach.

Xiong L, Chen Y, Chen L, Hua R, Shen N, Yang G Parasitol Res. 2023; 123(1):20.

PMID: 38072876 DOI: 10.1007/s00436-023-08016-w.


Eco-epidemiology triad to explain infectious diseases.

John T, Kompithra R Indian J Med Res. 2023; 158(2):107-112.

PMID: 37675687 PMC: 10645024. DOI: 10.4103/ijmr.ijmr_3031_21.


References
1.
Urban Jr J, Steenhard N, Solano-Aguilar G, Dawson H, Iweala O, Nagler C . Infection with parasitic nematodes confounds vaccination efficacy. Vet Parasitol. 2007; 148(1):14-20. PMC: 1959410. DOI: 10.1016/j.vetpar.2007.05.006. View

2.
Everts B, Perona-Wright G, Smits H, Hokke C, van der Ham A, Fitzsimmons C . Omega-1, a glycoprotein secreted by Schistosoma mansoni eggs, drives Th2 responses. J Exp Med. 2009; 206(8):1673-80. PMC: 2722183. DOI: 10.1084/jem.20082460. View

3.
Stadecker M, Asahi H, Finger E, Hernandez H, Rutitzky L, Sun J . The immunobiology of Th1 polarization in high-pathology schistosomiasis. Immunol Rev. 2004; 201:168-79. DOI: 10.1111/j.0105-2896.2004.00197.x. View

4.
Else K . Have gastrointestinal nematodes outwitted the immune system?. Parasite Immunol. 2005; 27(10-11):407-15. DOI: 10.1111/j.1365-3024.2005.00788.x. View

5.
Whelan M, Harnett M, Houston K, Patel V, Harnett W, Rigley K . A filarial nematode-secreted product signals dendritic cells to acquire a phenotype that drives development of Th2 cells. J Immunol. 2000; 164(12):6453-60. DOI: 10.4049/jimmunol.164.12.6453. View