Generation of a new therapeutic peptide that depletes myeloid-derived suppressor cells in tumor-bearing mice

Hong Qin, Beatrisa Lerman, Ippei Sakamaki, Guowei Wei, Soungchul C. Cha, Sheetal S. Rao, Jianfei Qian, Yared Hailemichael, Roza Nurieva, Karen C. Dwyer, Johannes Roth, Qing Yi, Willem W. Overwijk, Larry W. Kwak

Research output: Contribution to journalArticlepeer-review

119 Scopus citations


Immune evasion is an emerging hallmark of cancer progression. However, functional studies to understand the role of myeloid-derived suppressor cells (MDSCs) in the tumor microenvironment are limited by the lack of available specific cell surface markers. We adapted a competitive peptide phage display platform to identify candidate peptides binding MDSCs specifically and generated peptide-Fc fusion proteins (peptibodies). In multiple tumor models, intravenous peptibody injection completely depleted blood, splenic and intratumoral MDSCs in tumor-bearing mice without affecting proinflammatory immune cell types, such as dendritic cells. Whereas control Gr-1-specific antibody primarily depleted granulocytic MDSCs, peptibodies depleted both granulocytic and monocytic MDSC subsets. Peptibody treatment was associated with inhibition of tumor growth in vivo, which was superior to that achieved with Gr-1-specific antibody. Immunoprecipitation of MDSC membrane proteins identified S100 family proteins as candidate targets. Our strategy may be useful to identify new diagnostic and therapeutic surface targets on rare cell subtypes, including human MDSCs.

Original languageEnglish (US)
Pages (from-to)676-681
Number of pages6
JournalNature Medicine
Issue number6
StatePublished - Jun 2014

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology


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