The CD4+ T-cell help signal is transmitted from APC to CD8+ T-cells via CD27-CD70 interactions
被引:95
作者:
Feau, Sonia
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La Jolla Inst Allergy & Immunol, Cellular Immunol Lab, La Jolla, CA 92037 USALa Jolla Inst Allergy & Immunol, Cellular Immunol Lab, La Jolla, CA 92037 USA
Feau, Sonia
[1
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Garcia, Zacarias
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La Jolla Inst Allergy & Immunol, Cellular Immunol Lab, La Jolla, CA 92037 USALa Jolla Inst Allergy & Immunol, Cellular Immunol Lab, La Jolla, CA 92037 USA
Garcia, Zacarias
[1
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Arens, Ramon
[1
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Yagita, Hideo
[2
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Borst, Jannie
[3
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Schoenberger, Stephen P.
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La Jolla Inst Allergy & Immunol, Cellular Immunol Lab, La Jolla, CA 92037 USALa Jolla Inst Allergy & Immunol, Cellular Immunol Lab, La Jolla, CA 92037 USA
Schoenberger, Stephen P.
[1
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机构:
[1] La Jolla Inst Allergy & Immunol, Cellular Immunol Lab, La Jolla, CA 92037 USA
[2] Juntendo Univ, Sch Med, Dept Immunol, Bunkyo Ku, Tokyo 1138421, Japan
[3] Netherlands Canc Inst, Div Immunol, NL-1066 CX Amsterdam, Netherlands
CD8(+) cytotoxic T lymphocytes are critical components of immunity against infectious pathogens, tumours, and in the case of pathogenic autoimmunity, normal self tissues. CD4(+) T (T-H) cells provide 'help' to CD8(+) cytotoxic T lymphocytes during priming by first activating antigen-presenting cells via CD40-CD40L interactions. Here we show that, after immunization with either a noninflammatory, nonreplicating antigen or an overtly inflammatory replicating antigen, CD8(+) cytotoxic T lymphocytes prevented from receiving a signal through CD27 during priming subsequently exhibit a specific defect in their capacity for secondary expansion that can be rescued by the absence of TRAIL. Thus, the 'help message' is transmitted to CD8(+) T cells via CD70-CD27 signals, enabling them to undergo secondary expansion and avoid TRAIL-mediated apoptosis on re-stimulation. These findings complete our understanding of the cellular interactions through which T-H is provided to CD8(+) cytotoxic T lymphocytes during priming.
机构:
Univ Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, AIDS Inst, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
Elsaesser, Heidi
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Sauer, Karsten
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Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USAUniv Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
Sauer, Karsten
;
Brooks, David G.
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机构:
Univ Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, AIDS Inst, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
机构:
Univ Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, AIDS Inst, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
Elsaesser, Heidi
;
Sauer, Karsten
论文数: 0引用数: 0
h-index: 0
机构:
Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USAUniv Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
Sauer, Karsten
;
Brooks, David G.
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机构:
Univ Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, AIDS Inst, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA