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Tumor-Derived Vascular Pericytes Anergize Th Cells
Author(s) -
Anamika Bose,
Subhasis Barik,
Saptak Banerjee,
Tithi Ghosh,
Atanu Mallick,
Suchandra Bhattacharyya Majumdar,
Kuntal Kanti Goswami,
Avishek Bhuniya,
Sayantan Banerjee,
Rathindranath Baral,
Walter J. Storkus,
Partha Dasgupta,
Subrata Majumdar
Publication year - 2013
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1300280
Subject(s) - tumor microenvironment , immune system , biology , stromal cell , cancer research , microbiology and biotechnology , cancer immunotherapy , cd44 , immunotherapy , regulator , context (archaeology) , immunology , cell , gene , genetics , paleontology
Immune evasion within the tumor microenvironment supports malignant growth and is also a major obstacle for successful immunotherapy. Multiple cellular components and soluble factors coordinate to disrupt protective immune responses. Although stromal cells are well-known for their parenchymal supportive roles in cancer establishment and progression, we demonstrate for the first time, to our knowledge, that tumor-derived vascular pericytes negatively influence CD4(+) T cell activation and proliferation, and promote anergy in recall response to Ag by CD4(+)CD44(+) T cells via regulator of G protein signaling 5- and IL-6-dependent pathways. Our data support a new specific role for tumor-derived pericytes in the immune evasion paradigm within the tumor microenvironment and suggest the targeting of these cell populations in the context of successful immunotherapeutics for the treatment of cancer.

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