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Lack of general immunosuppression during visceral Leishmania tropica infection in BALB/c mice: augmented antibody response to thymus-independent antigens and polyclonal activation.

Abstract
Leishmania tropica causes a lethal visceral disease in highly susceptible BALB/c mice, with many immunopathologic features resembling those in human kala-azar. The responses to thymus-independent antigens of Type 1 and 2 (TI-1, TI-2) were compared in infected mice of susceptible BALB/c and resistant C57BL/6 strains at various times after infection. The infected BALB/c mice had an augmented response to both types of antigens at 45 days after infection. Later (day 76), the response to trinitrophenylated lipopolysaccharide (TNP-LPS, a TI-1 antigen) was diminished but that to dinitrophenylated Ficoll (DNP-Ficoll, a TI-2 antigen) remained statistically above the response of uninfected mice. The response of the resistant strain to either antigen was not modified as a result of the infection. Both strains showed significant polyclonal activation, which was considerably greater in the BALB/c than in the C57BL/6 mice. The observations presented here are in contrast to the widely held belief that a generalized nonspecific immunosuppression occurs in L. tropica infected BALB/c mice.
AuthorsJ H Colle, P Truffa-Bachi, L Chedid, F Modabber
JournalJournal of immunology (Baltimore, Md. : 1950) (J Immunol) Vol. 131 Issue 3 Pg. 1492-5 (Sep 1983) ISSN: 0022-1767 [Print] United States
PMID6350457 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens, T-Independent
  • DNP-Ficoll
  • Trinitrobenzenes
  • Ficoll
Topics
  • Animals
  • Antibody Formation
  • Antibody-Producing Cells (immunology)
  • Antigens, T-Independent (administration & dosage)
  • B-Lymphocytes (immunology)
  • Female
  • Ficoll (analogs & derivatives, immunology)
  • Hemolytic Plaque Technique
  • Kinetics
  • Leishmaniasis, Visceral (immunology)
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Trinitrobenzenes (immunology)

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