Mycobacterium bovis (BCG) Infection of the Lymph Nodes of Normal, Immune, and Cortisone-Treated Guinea Pigs 2

1977 ◽  
Vol 59 (5) ◽  
pp. 1527-1535 ◽  
Author(s):  
Frank M. Collins ◽  
Linda Auclair ◽  
George B. Mackaness
1980 ◽  
Vol 29 (3) ◽  
pp. 1034-1039 ◽  
Author(s):  
C C Shepard ◽  
R van Landingham ◽  
L L Walker

All mycobacteria species share some antigens, so there may be cultivable mycobacterial cultures that can provide vaccine protection against leprosy. Vaccine protection against Mycobacterium leprae infections in mice has been demonstrated for M. leprae itself, as living or heat-killed suspensions, and for Mycobacterium bovis (BCG), as living suspensions. Results are reported here with 17 other cultures. The mycobacterial suspensions were injected intradermally, and the mice were challenged in the footpad with infectious suspensions of M. leprae. In two experiments the mice were also challenged by footpad injections of 10(7) heat-killed M. leprae so the footpad enlargment could be measured. That some mycobacterial suspensions were immunogenic for some of their own antigens was suggested by reactions at the vaccine site and enlargement of the regional lymph nodes. Some mycobacterial suspensions also stimulated footpad enlargement on challenge by homologous suspensions or by challenge with M. leprae suspensions. Consistent protection against infectious challenge with M. leprae was observed only with BCG and M. leprae, however.


Vaccine ◽  
2004 ◽  
Vol 22 (8) ◽  
pp. 1063-1071 ◽  
Author(s):  
Mark A Chambers ◽  
D.Craig Wright ◽  
Joan Brisker ◽  
Ann Williams ◽  
Graham Hatch ◽  
...  

Tuberculosis ◽  
2007 ◽  
Vol 87 (2) ◽  
pp. 155-165 ◽  
Author(s):  
Toshiko Yamamoto ◽  
Todd M. Lasco ◽  
Kazuyuki Uchida ◽  
Yoshitaka Goto ◽  
Amminikutty Jeevan ◽  
...  

1980 ◽  
Vol 28 (3) ◽  
pp. 887-892
Author(s):  
E Yarkoni ◽  
H J Rapp

Mycobacterium bovis (BCG), Mycobacterium phlei, and Mycobacterium smegmatis were each tested in emulsified form for their potency to cause regression of transplants of a syngeneic murine fibrosarcoma and of a syngeneic guinea pig hepatoma. On a weight basis, M. phlei and M. smegmatis were as effective as BCG in causing tumor regression. M. phlei and M. smegmatis were comparable to BCG in provoking delayed cutaneous hypersensitivity reactions in guinea pigs sensitized to M. phlei or M. smegmatis. In BCG-sensitized guinea pigs, M. phlei and M. smegmatis provoked weaker delayed cutaneous hypersensitivity reactions than did BCG. Purified protein derivative of M. tuberculosis was more active in eliciting delayed cutaneous hypersensitivity in BCG-sensitized guinea pigs than in animals sensitized with M. phlei or M. smegmatis.


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