Literature DB >> 1877714

Eosinophil-rich, granulomatous inflammatory response to Plasmodium berghei hepatic schizonts in nonimmunized rats is age-related.

Z M Khan1, J P Vanderberg.   

Abstract

Inflammatory responses to Plasmodium hepatic schizonts within the livers of non-immunized animals have long been assumed to be initiated only after the parasites have matured and begun to burst. However, recent reports of inflammatory responses around hepatic schizonts suggested a re-examination of this issue. We injected Norway-Brown rats of various ages intravenously with Plasmodium berghei sporozoites and studied subsequent liver histopathology. We found that the ability of these rats to mount an inflammatory response is age-dependent. Young (4 weeks) rats had weak inflammatory responses against hepatic schizonts, whereas older (8-10 weeks) rats mounted a strong response. Older rats had many granulomatous reactions within the liver; eosinophils represented a pioneer component of the cellular infiltrate. There was a reduction in the numbers of surviving hepatic schizonts in the older rats, suggesting that these granulomatous and eosinophilic reactions had effectively destroyed some of the hepatic schizonts. We found clear evidence of inflammatory cells (eosinophils) infiltrating hepatic schizonts as early as 40 hours post-injection with sporozoites, a time well before any hepatic schizonts could have burst within the liver. This presents histological evidence that inflammatory cells can recognize and infiltrate intact hepatocytes containing schizonts in immunologically naive animals.

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Year:  1991        PMID: 1877714     DOI: 10.4269/ajtmh.1991.45.190

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  7 in total

1.  Early hepatic stages of Plasmodium berghei: release of circumsporozoite protein and host cellular inflammatory response.

Authors:  Z M Khan; C Ng; J P Vanderberg
Journal:  Infect Immun       Date:  1992-01       Impact factor: 3.441

2.  Inhibition of nitric oxide interrupts the accumulation of CD8+ T cells surrounding Plasmodium berghei-infected hepatocytes.

Authors:  L F Scheller; S J Green; A F Azad
Journal:  Infect Immun       Date:  1997-09       Impact factor: 3.441

3.  Exoerythrocytic development of Plasmodium gallinaceum in the White Leghorn chicken.

Authors:  Ute Frevert; Gerald F Späth; Herman Yee
Journal:  Int J Parasitol       Date:  2007-10-12       Impact factor: 3.981

Review 4.  Immunity to liver stage malaria: considerations for vaccine design.

Authors:  Andrew W Taylor-Robinson
Journal:  Immunol Res       Date:  2003       Impact factor: 2.829

Review 5.  Plasmodium cellular effector mechanisms and the hepatic microenvironment.

Authors:  Ute Frevert; Urszula Krzych
Journal:  Front Microbiol       Date:  2015-05-27       Impact factor: 5.640

6.  Chickens treated with a nitric oxide inhibitor became more resistant to Plasmodium gallinaceum infection due to reduced anemia, thrombocytopenia and inflammation.

Authors:  Barbarella Matos de Macchi; Farlen José Bebber Miranda; Fernanda Silva de Souza; Eulógio Carlos Queiroz de Carvalho; Antônio Peixoto Albernaz; José Luiz Martins do Nascimento; Renato Augusto DaMatta
Journal:  Vet Res       Date:  2013-02-11       Impact factor: 3.683

7.  Release of hepatic Plasmodium yoelii merozoites into the pulmonary microvasculature.

Authors:  Kerstin Baer; Christian Klotz; Stefan H I Kappe; Thomas Schnieder; Ute Frevert
Journal:  PLoS Pathog       Date:  2007-11       Impact factor: 6.823

  7 in total

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