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Cited by 240

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Direct activation of CD8+ cytotoxic T lymphocytes by dendritic cells.

Open access
Inaba, K, Young, J W, Steinman, R M·1987·The Journal of experimental medicine

Abstract

Recent experiments (11-13) have shown that antigen-specific, CD8+, CD4- T lymphocytes can be induced to proliferate and become killer cells in the absence of a second population of "helper" CD8-, CD4+ cells. We have studied early events in the activation of CD4+ and CD8+ T cell subsets in the primary mixed leukocyte reaction. Dendritic cells are a major if not essential accessory cell for the activation of both subpopulations. Antigen-bearing macrophages fail to stimulate unprimed CD8+ cells, but act as targets for the sensitized cytolytic lymphocytes that are induced by dendritic cells. The initial proliferative response is comparable for CD4+ and CD8+ lymphocyte subsets. For both subpopulations, dendritic cells efficiently cluster the responding lymphocytes on the first day and induce the release of IL-2. The data indicate that CD4+ and CD8+ lymphocytes can be activated by a similar mechanism, and illustrate the special role of dendritic cells in the sensitization stage of cell-mediated immunity.

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Metadata

Authors
Inaba, K., Young, J. W., & Steinman, R. M.
Venue
The Journal of experimental medicine
Published
1987-07-01
Volume
166
Issue
1
Pages
182-194
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2083873864
Cited by
240
References
0
FWCI
6.74
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Direct activation of CD8+ cytotoxic T lymphocytes by dendritic cells. https://app.cochat.ai/papers/10.1084/jem.166.1.182
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Inaba, K., Young, J. W., & Steinman, R. M. (1987). Direct activation of CD8+ cytotoxic T lymphocytes by dendritic cells. The Journal of experimental medicine. https://doi.org/10.1084/jem.166.1.182

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.