Trypanosoma congolense: proliferative responses and interleukin production in lymph node cells of infected cattle

V Lutje1, B Mertens, A Boulangé

  • 1International Livestock Research Institute (ILRI), Nairobi, Kenya.

Experimental Parasitology
|September 1, 1995
PubMed

Insights

Cattle infected with Trypanosoma congolense mount T-cell immune responses primarily in lymph nodes, not blood, against specific parasite antigens. These responses peak early and involve key immune signaling molecules.

Area of Science:

  • Veterinary Immunology
  • Parasitology
  • Molecular Biology

Background:

  • Trypanosoma congolense causes significant disease in cattle.
  • Understanding the host immune response is crucial for developing effective control strategies.
  • T-cell responses are vital for controlling parasitic infections.

Purpose of the Study:

  • To investigate T-cell-mediated immune responses in cattle during primary Trypanosoma congolense infection.
  • To identify specific parasite antigens that elicit cellular immune responses.
  • To determine the location and characteristics of these T-cell responses.

Main Methods:

  • Cattle were infected with Trypanosoma congolense.
  • Lymph node cells and peripheral blood mononuclear cells were isolated.
  • Antigen-specific proliferation assays were performed using variable surface glycoprotein, congopain, and heat-shock protein.
  • Cytokine production (IL-2, IFN-gamma) and mRNA expression (IL-2, IL-4, IFN-gamma) were analyzed.

Main Results:

  • Highest proliferative T-cell responses were observed in the second week post-infection.
  • Significant responses were detected in lymph node cells draining the infection site, but not in peripheral blood.
  • Antigen stimulation induced production of IL-2 and IFN-gamma in lymph node cells.
  • Expression of IL-2, IL-4, and IFN-gamma mRNA was confirmed in stimulated lymph node cells.

Conclusions:

  • Cattle mount a localized T-cell immune response in draining lymph nodes against Trypanosoma congolense antigens during primary infection.
  • The cellular immune response involves the production of key cytokines like IL-2 and IFN-gamma.
  • Invariant antigens like congopain and heat-shock protein are targets of the T-cell response, alongside VSG.

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