Contribution of tumour necrosis factor-alpha (TNF-α) in host defence mechanism against Cryptococcus neoformans

K. Kawakami, X. Qifeng, M. Tohyama, M. H. Qureshi, A. Saito

研究成果: Article査読

69 被引用数 (Scopus)

抄録

We investigated the role of TNF-α in the host defence mechanism against infection with a virulent strain of Cryptococcus neoformans. Administration of exogenous recombinant human TNF-α significantly prolonged the survival time of mice infected by intratracheal instillation of the organism. Surprisingly, neutralizing MoAb to murine TNF-α did not shorten their survival time, a finding inconsistent with previous results. To investigate the cause of this inconsistency, we examined the production of TNF-α in the lungs of infected mice. During the course of cryptococcosis, there was little or no generation of TNF-αmRNA in the lung. This might be partly due to a direct inhibitory action of the fungal microorganism on TNF-α production by macrophages. In vitro production of TNF-α by murine interferon-gamma (IFN-γ)- and lipopolysaccharide (LPS)stimulated macrophages was strongly inhibited by co-culturing with the whole yeast cells. In contrast, administration of recombinant murine IL-12 markedly induced TNF-α production and the neutralizing anti-TNF-α MoAb strongly blocked IL-12-induced protection of mice against cryptococcal infection. These results indicate that endogenously synthesized TNF-α has the potential to contribute to the elimination of C. neoformans and partly mediates the protective effect of IL-12.

本文言語English
ページ(範囲)468-474
ページ数7
ジャーナルClinical and Experimental Immunology
106
3
DOI
出版ステータスPublished - 1996
外部発表はい

ASJC Scopus subject areas

  • 免疫アレルギー学
  • 免疫学

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