Nippostrongylus brasiliensis: observations on factors affecting the establishment of secondary worm populations in rats

Parasitology ◽  
1974 ◽  
Vol 68 (1) ◽  
pp. 13-17 ◽  
Author(s):  
D. Conwil Jenkins

Previously immunized rats of different ages were exposed either to one large, or several small challenge infections with the nematode, Nippostrongylus brasiliensis. The number of secondary worms harboured by each of these rats was then determined on the fourteenth day after exposure to challenge. It was found that worms adapted more efficiently to host immunity when both (a) the rats were less than 11 weeks old when challenged and (b) the challenge was given in small repeated doses over a period of weeks. The age of the rats on exposure to the immunizing primary infection, however, had little or no affect per se on the subsequent establishment of immune-adapted worms. It is tentatively suggested that the failure of worms to adapt effectively to the acquired immunity of older rats resulted from the acquisition by these rats of a fully competent cellular immune response.

Parasitology ◽  
1973 ◽  
Vol 66 (1) ◽  
pp. 199-205 ◽  
Author(s):  
E. Harness ◽  
K. Smith ◽  
Patricia Bland

The structure of H. placei adult worms, obtained from calves at 4, 7, 10 or 11–13 weeks after primary infection, has been studied. A reorganization of rough endoplasmic reticuhim in the cytoplasm of the gut cells was seen at 10 weeks and this was followed by marked vacuolation of many of these cells, associated with an increase in lipid production. Increases of lipid were also found in the hypodermis, lateral cords and occasionally muscle cells of worms examined at 11–13 weeks after infection.It is suggested that these changes are the result of the host immune response, because they resemble changes which occur in the rat nematode Nippostrongylus brasiliensis and which are known to be caused by host immunity.


2002 ◽  
Vol 6 (2) ◽  
pp. 125-128 ◽  
Author(s):  
Beatríz Sierra ◽  
Gissel García ◽  
Ana B. Pérez ◽  
Luis Morier ◽  
Rayner Rodríguez ◽  
...  

1999 ◽  
Vol 37 (2) ◽  
pp. 123-129 ◽  
Author(s):  
B. R. Mignon ◽  
T. Leclipteux ◽  
CH. Focant ◽  
A. J. Nikkels ◽  
G. E. PIErard ◽  
...  

2004 ◽  
Vol 146 (4) ◽  
pp. 159-172 ◽  
Author(s):  
D. Müller-Doblies ◽  
S. Baumann ◽  
P. Grob ◽  
A. Hülsmeier ◽  
U. Müller-Doblies ◽  
...  

2005 ◽  
Vol 102 (Special_Supplement) ◽  
pp. 180-184 ◽  
Author(s):  
György T. Szeifert ◽  
Isabelle Salmon ◽  
Sandrine Rorive ◽  
Nicolas Massager ◽  
Daniel Devriendt ◽  
...  

Object. The aim of this study was to analyze the cellular immune response and histopathological changes in secondary brain tumors after gamma knife surgery (GKS). Methods. Two hundred ten patients with cerebral metastases underwent GKS. Seven patients underwent subsequent craniotomy for tumor removal between 1 and 33 months after GKS. Four of these patients had one tumor, two patients had two tumors, and one patient had three. Histological and immunohistochemical investigations were performed. In addition to routine H & E and Mallory trichrome staining, immunohistochemical reactions were conducted to characterize the phenotypic nature of the cell population contributing to the tissue immune response to neoplastic deposits after radiosurgery. Light microscopy revealed an intensive lymphocytic infiltration in the parenchyma and stroma of tumor samples obtained in patients in whom surgery was performed over 6 months after GKS. Contrary to this, extensive areas of tissue necrosis with either an absent or scanty lymphoid population were observed in the poorly controlled neoplastic specimens obtained in cases in which surgery was undertaken in patients less than 6 months after GKS. Immunohistochemical characterization demonstrated the predominance of CD3-positive T cells in the lymphoid infiltration. Conclusions. Histopathological findings of the present study are consistent with a cellular immune response of natural killer cells against metastatic brain tumors, presumably stimulated by the ionizing energy of focused radiation.


Sign in / Sign up

Export Citation Format

Share Document