Spleen cell cytokine secretion in Mycobacterium bovis BCG-infected mice

Kris Huygen(Institut Belge pour la Sécurité Routière), Daniel Abramowicz(Institut Belge pour la Sécurité Routière), Pierre-Yves Vandenbussche(Institut Belge pour la Sécurité Routière), F. Jacobs(Institut Belge pour la Sécurité Routière), Jacqueline De Bruyn(Institut Belge pour la Sécurité Routière), Alain Kentos(Institut Belge pour la Sécurité Routière), Annie Drowart(Institut Belge pour la Sécurité Routière), J P Van Vooren(Institut Belge pour la Sécurité Routière), Michel Goldman(Institut Belge pour la Sécurité Routière)
Infection and Immunity
July 1, 1992
Cited by 168Open Access
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Abstract

Three susceptible mouse strains, i.e., BALB/c (H-2d), C57BL/6 (H-2b), and major histocompatibility complex-congenic BALB.B10 (H-2b), were infected intravenously with 4 x 10(6) CFU of live Mycobacterium bovis BCG and analyzed 4 weeks later for in vitro spleen cell cytokine secretion in response to purified protein derivative (PPD), BCG culture filtrate (CF), BCG cellular extract, total BCG, the purified extracellular 30-32-kDa antigen (the fibronectin-binding antigen 85), or the intracellular 65-kDa heat shock protein. C57BL/6 and BALB.B10 mice produced 5- to 10-fold more gamma interferon and interleukin-2 (IL-2) when stimulated with CF, PPD, and antigen 85 than BALB/c mice did. When stimulated with BCG extract and whole BCG, gamma interferon and IL-2 levels were generally lower and comparable in the three strains. IL-4 was detected in spleen cell culture supernatants from infected BALB/c mice but not from C57BL/6 or BALB.B10 mice. IL-5 could not be detected. C57BL/6 and BALB.B10 spleen cells also produced more tumor necrosis factor alpha and IL-6 after stimulation with PPD and CF than BALB/c cells did. Finally, BCG vaccination generated efficient protective immunity in C57BL/6 and BALB.B10 mice but not in BALB/c mice. These data suggest that secreted mycobacterial CF antigens selectively induce a strong TH1 response in BCG-infected C57BL/6 and BALB.B10 mice, whereas in BALB/c mice this response is partly counterbalanced by TH2 cells.


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