Literature DB >> 22710310

Using eggs from Schistosoma mansoni as an in vivo model of helminth-induced lung inflammation.

Karen L Joyce1, Will Morgan, Robert Greenberg, Meera G Nair.   

Abstract

Schistosoma parasites are blood flukes that infect an estimated 200 million people worldwide. In chronic infection with Schistosoma, the severe pathology, including liver fibrosis and splenomegaly, is caused by the immune response to the parasite eggs rather than the parasite itself. Parasite eggs induce a Th2 response characterized by the production of IL-4, IL-5 and IL-13, the alternative activation of macrophages and the recruitment of eosinophils. Here, we describe injection of Schistosoma mansoni eggs as a model to examine parasite-specific Th2 cytokine responses in the lung and draining lymph nodes, the formation of pulmonary granulomas surrounding the egg, and airway inflammation. Following intraperitoneal sensitization and intravenous challenge, S. mansoni eggs are transported to the lung via the pulmonary arteries where they are trapped within the lung parenchyma by granulomas composed of lymphocytes, eosinophils and alternatively activated macrophages. Associated with granuloma formation, inflammation in the broncho-alveolar spaces, expansion of the draining lymph nodes and CD4 T cell activation can be observed. Here we detail the protocol for isolating Schistosoma mansoni eggs from infected livers (modified from), sensitizing and challenging mice, and recovering the organs (broncho-alveolar lavage (BAL), lung and draining lymph nodes) for analysis. We also include representative histologic and immunologic data and suggestions for additional immunologic analysis. Overall, this method provides an in vivo model to investigate helminth-induced immunologic responses in the lung, which is broadly applicable to the study of Th2 inflammatory diseases including helminth infection, fibrotic diseases, allergic inflammation and asthma. Advantages of this model for the study of type 2 inflammation in the lung include the reproducibility of a potent Th2 inflammatory response in the lung and draining lymph nodes, the ease of assessment of inflammation by histologic examination of the granulomas surrounding the egg, and the potential for long-term storage of the parasite eggs.

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Year:  2012        PMID: 22710310      PMCID: PMC3471298          DOI: 10.3791/3905

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  13 in total

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Journal:  World Health Organ Tech Rep Ser       Date:  2002

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Journal:  Nat Rev Immunol       Date:  2004-08       Impact factor: 53.106

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Journal:  J Immunol       Date:  1998-02-15       Impact factor: 5.422

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Journal:  J Parasitol       Date:  1986-12       Impact factor: 1.276

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Journal:  Am J Trop Med Hyg       Date:  1987-07       Impact factor: 2.345

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Journal:  J Immunol       Date:  2003-10-01       Impact factor: 5.422

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Authors:  Matyas Sandor; Joel V Weinstock; Thomas A Wynn
Journal:  Trends Immunol       Date:  2003-01       Impact factor: 16.687

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Authors:  F Lewis
Journal:  Curr Protoc Immunol       Date:  2001-05

10.  IL-31-IL-31R interactions negatively regulate type 2 inflammation in the lung.

Authors:  Jacqueline G Perrigoue; Ji Li; Colby Zaph; Michael Goldschmidt; Phillip Scott; Frederic J de Sauvage; Edward J Pearce; Nico Ghilardi; David Artis
Journal:  J Exp Med       Date:  2007-03-12       Impact factor: 14.307

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  7 in total

1.  CD14 influences host immune responses and alternative activation of macrophages during Schistosoma mansoni infection.

Authors:  Smanla Tundup; Leena Srivastava; Tamas Nagy; Donald Harn
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Review 2.  Th2 responses in schistosomiasis.

Authors:  Keke Fairfax; Marcia Nascimento; Stanley Ching-Cheng Huang; Bart Everts; Edward J Pearce
Journal:  Semin Immunopathol       Date:  2012-11-09       Impact factor: 9.623

Review 3.  Schistosomes in the Lung: Immunobiology and Opportunity.

Authors:  Emma L Houlder; Alice H Costain; Peter C Cook; Andrew S MacDonald
Journal:  Front Immunol       Date:  2021-04-19       Impact factor: 7.561

4.  HIV and Schistosoma Co-Exposure Leads to Exacerbated Pulmonary Endothelial Remodeling and Dysfunction Associated with Altered Cytokine Landscape.

Authors:  Sandra Medrano-Garcia; Daniel Morales-Cano; Bianca Barreira; Alba Vera-Zambrano; Rahul Kumar; Djuro Kosanovic; Ralph Theo Schermuly; Brian B Graham; Francisco Perez-Vizcaino; Alistair Mathie; Rajkumar Savai; Soni Pullamseti; Ghazwan Butrous; Edgar Fernández-Malavé; Angel Cogolludo
Journal:  Cells       Date:  2022-08-04       Impact factor: 7.666

5.  Vitamin A mediates conversion of monocyte-derived macrophages into tissue-resident macrophages during alternative activation.

Authors:  Uma Mahesh Gundra; Natasha M Girgis; Michael A Gonzalez; Mei San Tang; Hendrik J P Van Der Zande; Jian-Da Lin; Mireille Ouimet; Lily J Ma; Jordan Poles; Nikollaq Vozhilla; Edward A Fisher; Kathryn J Moore; P'ng Loke
Journal:  Nat Immunol       Date:  2017-04-24       Impact factor: 25.606

6.  Helminth-induced IL-4 expands bystander memory CD8+ T cells for early control of viral infection.

Authors:  Marion Rolot; Annette M Dougall; Alisha Chetty; Justine Javaux; Ting Chen; Xue Xiao; Bénédicte Machiels; Murray E Selkirk; Rick M Maizels; Cornelis Hokke; Olivier Denis; Frank Brombacher; Alain Vanderplasschen; Laurent Gillet; William G C Horsnell; Benjamin G Dewals
Journal:  Nat Commun       Date:  2018-10-30       Impact factor: 14.919

7.  Chronic schistosomiasis suppresses HIV-specific responses to DNA-MVA and MVA-gp140 Env vaccine regimens despite antihelminthic treatment and increases helminth-associated pathology in a mouse model.

Authors:  Godfrey A Dzhivhuho; Samantha A Rehrl; Hlumani Ndlovu; William G C Horsnell; Frank Brombacher; Anna-Lise Williamson; Gerald K Chege
Journal:  PLoS Pathog       Date:  2018-07-26       Impact factor: 6.823

  7 in total

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