Functional characterization of human Cd33+ And Cd11b+ myeloid-derived suppressor cell subsets induced from peripheral blood mononuclear cells co-cultured with a diverse set of human tumor cell lines
2011

Understanding Myeloid-Derived Suppressor Cells in Cancer

Sample size: 61 publication 10 minutes Evidence: moderate

Author Information

Author(s): Melissa G. Lechner, Carolina Megiel, Sarah M. Russell, Brigid Bingham, Tammy Woo, Alan L. Epstein

Primary Institution: USC Keck School of Medicine

Hypothesis

Can human tumor cell lines induce myeloid-derived suppressor cells (MDSC) from peripheral blood mononuclear cells?

Conclusion

The study identifies two distinct subsets of MDSC induced by various human solid tumors, which could inform new cancer therapies.

Supporting Evidence

  • 45 out of 101 tumor cell lines induced CD33+ MDSC.
  • CD33+ MDSC induction was significantly correlated with the expression of IL-1β, IL-6, TNFα, VEGF, and GM-CSF.
  • Breast cancer cell lines did not induce CD33+ MDSC.
  • CD11b+ MDSC were induced by FLT3L and TGFβ from certain tumor cell lines.
  • Both MDSC subsets showed up-regulation of suppressive genes like ARG-1 and iNOS.

Takeaway

This study shows that certain cancer cells can make special immune cells that help tumors grow by stopping the body's defenses.

Methodology

The study used in vitro co-culture methods to induce MDSC from healthy donor PBMC with various human tumor cell lines.

Potential Biases

Potential bias in selecting tumor cell lines and donor variability.

Limitations

The study primarily focuses on in vitro findings, which may not fully replicate in vivo conditions.

Participant Demographics

39 male and 22 female healthy volunteers aged 23 to 62.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1479-5876-9-90

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