Tumor Induces the Expansion of Foxp3+CD25high and CD11b+Gr-1+ Cell Population in the Early Phase of Tumor Progression
Author:
Affiliation:
1. Department of Biomedical Laboratory Science, Soon Chun Hyang University, Asan 31538, Korea
2. Department of Biomedical Laboratory Science, Korea Nazarene University, Cheonan 31172, Korea
Funder
National Research Foundation of Korea(NRF)
Publisher
The Korean Society for Biomedical Laboratory Sciences
Subject
General Medicine
Link
http://pdf.medrang.co.kr/BSL/2015/021/bsl-21-172.pdf
Reference23 articles.
1. Bronte, V, Apolloni, E, Cabrelle, A, Ronca, R, Serafini, P, Zamboni, P, Restifo, NP, and Zanovello, P (2000). Identification of a CD11b(+)/ Gr-1(+)/D31(+) myeloid progenitor capable of activating or suppressing CD8(+) T cells. Blood. 96, 3838-3846.
2. Natural and Induced T CD4+CD25+FOXP3+ Regulatory T Cells
3. NK cell-based immunotherapy for malignant diseases
4. The Tumoricidal Activity of Memory CD8+T Cells Is Hampered by Persistent Systemic Antigen, but Full Functional Capacity Is Regained in an Antigen-Free Environment
5. Increased Memory Conversion of Naïve CD8 T Cells Activated during Late Phases of Acute Virus Infection Due to Decreased Cumulative Antigen Exposure
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