Journal
INFECTION AND IMMUNITY
Volume 75, Issue 1, Pages 193-200Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/IAI.01148-06
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Funding
- NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [P01AI061298, R37AI042747, R01AI040996, R01AI034361] Funding Source: NIH RePORTER
- NIAID NIH HHS [AI-61298, P01 AI061298, R01 AI040996, AI-40996, R37 AI042747, AI-34361, AI-42747, R01 AI034361] Funding Source: Medline
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Immunization with a cell wall/membrane (CW/M) and yeast cytosol extract (YCE) crude antigen from Blastomyces dermatitidis confers T-cell-mediated resistance against lethal experimental infection in mice. We isolated and characterized T cells that recognize components of these protective antigens and mediate protection. CD4(+) T-cell clones elicited with CW/M antigen adoptively transferred protective immunity when they expressed a V alpha 2(+) J alpha 49(+)/V beta 1(+) J beta 1.1(+) heterodimeric T-cell receptor (TCR) and produced high levels of gamma interferon (IFN-gamma). In contrast, V beta 8.1/8.2(+) CD4(+) T-cell clones that were reactive against CW/M and YCE antigens and produced little or no IFN-gamma either failed to mediate protection or exacerbated the infection depending on the level of interleukin-5 expression. Thus, the outgrowth of protective T-cell clones against immunodominant antigens of B. dermatitidis is biased by a combination of the TCR repertoire and Th1 cytokine production.
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