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CD29 enriches for cytotoxic human CD4+T cells
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ABSTRACTCD4+T cell are key contributors in the induction of adaptive immune responses against pathogens. Even though CD4+T cells are primarily classified as non-cytotoxic helper T cells, it has become appreciated that a subset of CD4+T cells is cytotoxic. However, tools to identify these cytotoxic CD4+T cells are lacking. We recently showed that CD29 (Integrin Beta 1, ITGB1) expression on human CD8+T cells enriches for the most potent cytotoxic T cells. Here, we questioned whether CD29 expression also associates with cytotoxic CD4+T cells. We show that human peripheral blood-derived CD29hiCD4+T cells display a cytotoxic gene expression profile, which closely resembles that of CD29hicytotoxic CD8+T cells. This CD29hicytotoxic phenotype was observedex vivoand was maintained inin vitrocultures. CD29 expression enriched for CD4+T cells, which effectively produced the pro-inflammatory cytokines IFN-γ, IL-2, and TNF-α, and cytotoxic molecules. Lastly, CD29-expressing CD4+T cells transduced with a MART-1 specific TCR showed target cell killingin vitro. In conclusion, we here demonstrate that CD29 can be employed to enrich for cytotoxic human CD4+T cells.
Title: CD29 enriches for cytotoxic human CD4+T cells
Description:
ABSTRACTCD4+T cell are key contributors in the induction of adaptive immune responses against pathogens.
Even though CD4+T cells are primarily classified as non-cytotoxic helper T cells, it has become appreciated that a subset of CD4+T cells is cytotoxic.
However, tools to identify these cytotoxic CD4+T cells are lacking.
We recently showed that CD29 (Integrin Beta 1, ITGB1) expression on human CD8+T cells enriches for the most potent cytotoxic T cells.
Here, we questioned whether CD29 expression also associates with cytotoxic CD4+T cells.
We show that human peripheral blood-derived CD29hiCD4+T cells display a cytotoxic gene expression profile, which closely resembles that of CD29hicytotoxic CD8+T cells.
This CD29hicytotoxic phenotype was observedex vivoand was maintained inin vitrocultures.
CD29 expression enriched for CD4+T cells, which effectively produced the pro-inflammatory cytokines IFN-γ, IL-2, and TNF-α, and cytotoxic molecules.
Lastly, CD29-expressing CD4+T cells transduced with a MART-1 specific TCR showed target cell killingin vitro.
In conclusion, we here demonstrate that CD29 can be employed to enrich for cytotoxic human CD4+T cells.
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