B7-H4, a molecule of the B7 family, negatively regulates T cell immunity.
By G. Sica, I. Choi, G. Zhu, K. Tamada, Shengxi Wang, H. Tamura, A. Chapoval, D. Flies, Jürgen Bajorath, Lieping Chen. Immunity, 2003
724 citations recorded by the source corpus.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/7ce46d0756484dbf41397ca3d0bfb0587f95d53e
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Citations in the corpus
- Immunosuppressive networks in the tumour environment and their therapeutic relevance (2005, background): “B7-H4 was shown to be a negative regulator of T-cell responses in vitro by inhibiting T-cell proliferation, cell-cycle progression and cytokine productio”
- B7-H4 expression identifies a novel suppressive macrophage population in human ovarian carcinoma (2006, background): “Antigen-specifi c T cell responses are impaired in mice treated with a B7-H4Ig fusion protein (22).”
- Inhibitory B7-family molecules in the tumour microenvironment (2008, background): “B7-H4 was also identified by DNA sequence homology to other B7 molecule”
- B and T lymphocyte attenuator regulates T cell activation through interaction with herpesvirus entry mediator (2005, background): “There has been an indirect indication that the B7 family member B7x (also identified as B7S1 and B7-H4”
- Co-inhibitory molecules of the B7–CD28 family in the control of T-cell immunity (2004, background): “Emerging co-inhibitors: B7-H4 and BTLA B7-H4 (B7S1, B7X) is a recently identified B7-family member with co-inhibitory functio”