TY - JOUR
T1 - B7-H1-dependent sex-related differences in tumor immunity and immunotherapy responses
AU - Lin, Pei Yi
AU - Sun, Lishi
AU - Thibodeaux, Suzanne R.
AU - Ludwig, Sara M.
AU - Vadlamudi, Ratna K.
AU - Hurez, Vincent J.
AU - Bahar, Rumana
AU - Kious, Mark J.
AU - Livi, Carolina B.
AU - Wall, Shawna R.
AU - Chen, Lieping
AU - Zhang, Bin
AU - Shin, Tahiro
AU - Curiel, Tyler J.
PY - 2010/9/1
Y1 - 2010/9/1
N2 - CD4+CD25+Foxp3+ regulatory T cells (Tregs) are immunopathogenic in cancers by impeding tumor-specific immunity. B7-homologue 1 (B7-H1) (CD274) is a cosignaling molecule with pleiotropic effects, including hindering antitumor immunity. In this study, we demonstrate sex-dependent, B7-H1-dependent differences in tumor immunity and response to immunotherapy in a hormone-independent cancer, murine B16 melanoma. Antitumor immunity was better in B7-H1-/- females versus males as a result of reduced regulatory T cell function in the B7-H1-/- females, and clinical response following B7-H1 blockade as tumor immunotherapy was significantly better in wild-type females than in males, owing to greater B7-H1 blockade-mediated reduction of Treg function in females. Wild-type female Tregs expressed significantly lower B7-H1 versus males but were insensitive to estrogen in vitro. Female B7-H1-/- Tregs were exquisitely sensitive to estrogen-mediated functional reduction in vitro, suggesting that B7-H1 effects occur before terminal Treg differentiation. Immune differences were independent of known B7-H1 ligands. Sex-dependent immune differences are seldom considered in designing immune therapy or interpreting immunotherapy treatment results. Our data demonstrate that sex is an important variable in tumor immunopathogenesis and immunotherapy responses through differential Treg function and B7-H1 signaling.
AB - CD4+CD25+Foxp3+ regulatory T cells (Tregs) are immunopathogenic in cancers by impeding tumor-specific immunity. B7-homologue 1 (B7-H1) (CD274) is a cosignaling molecule with pleiotropic effects, including hindering antitumor immunity. In this study, we demonstrate sex-dependent, B7-H1-dependent differences in tumor immunity and response to immunotherapy in a hormone-independent cancer, murine B16 melanoma. Antitumor immunity was better in B7-H1-/- females versus males as a result of reduced regulatory T cell function in the B7-H1-/- females, and clinical response following B7-H1 blockade as tumor immunotherapy was significantly better in wild-type females than in males, owing to greater B7-H1 blockade-mediated reduction of Treg function in females. Wild-type female Tregs expressed significantly lower B7-H1 versus males but were insensitive to estrogen in vitro. Female B7-H1-/- Tregs were exquisitely sensitive to estrogen-mediated functional reduction in vitro, suggesting that B7-H1 effects occur before terminal Treg differentiation. Immune differences were independent of known B7-H1 ligands. Sex-dependent immune differences are seldom considered in designing immune therapy or interpreting immunotherapy treatment results. Our data demonstrate that sex is an important variable in tumor immunopathogenesis and immunotherapy responses through differential Treg function and B7-H1 signaling.
UR - http://www.scopus.com/inward/record.url?scp=78049406865&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.1000496
DO - 10.4049/jimmunol.1000496
M3 - Article
C2 - 20686128
AN - SCOPUS:78049406865
SN - 0022-1767
VL - 185
SP - 2747
EP - 2753
JO - Journal of Immunology
JF - Journal of Immunology
IS - 5
ER -