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Alex Yee-Chen Huang

Researcher at Case Western Reserve University

Publications -  107
Citations -  7986

Alex Yee-Chen Huang is an academic researcher from Case Western Reserve University. The author has contributed to research in topics: Immune system & T cell. The author has an hindex of 35, co-authored 98 publications receiving 7137 citations. Previous affiliations of Alex Yee-Chen Huang include University of Chicago & National Institutes of Health.

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Role of bone marrow-derived cells in presenting MHC class I-restricted tumor antigens

TL;DR: MHC class I-restricted antigens are efficiently transferred in vivo to bone marrow-derived antigen-presenting cells, which suggests that human leukocyte antigen matching may be less critical in the application of tumor vaccines than previously thought.
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Chemokines enhance immunity by guiding naive CD8 + T cells to sites of CD4 + T cell–dendritic cell interaction

TL;DR: It is demonstrated that after immunization but before antigen recognition, naive CD8+ T cells in immunogen-draining lymph nodes upregulate the chemokine receptor CCR5, permitting these cells to be attracted to sites of antigen-specific dendritic cell–CD4+ T cell interaction where the cognate chemokines CCL3 and CCL4 are produced.
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Dynamic imaging of dendritic cell extension into the small bowel lumen in response to epithelial cell TLR engagement

TL;DR: Findings support a model in which epithelial cell TLR signaling upon exposure to microbial stimuli induces active DC sampling of the gut lumen at sites distant from organized lymphoid tissues.
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Extrafollicular Activation of Lymph Node B Cells by Antigen-Bearing Dendritic Cells

TL;DR: It is shown that, after exiting high-endothelial venules and before entry into lymph node follicles, B cells survey locally concentrated dendritic cells, suggesting a possible role for antigen-specific B-DC interactions in promoting T cell–dependent antibody responses in vivo.
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The immunodominant major histocompatibility complex class I-restricted antigen of a murine colon tumor derives from an endogenous retroviral gene product.

TL;DR: Adoptive transfer with CTL lines specific for this antigen demonstrated that this epitope represents a potent tumor rejection antigen, providing evidence for a unique class of shared immunodominant tumor associated antigens as targets for antitumor immunity.