TY - JOUR
T1 - Parity and lactation induce T cell mediated breast cancer protection
AU - kConFab consortium
AU - Virassamy, Balaji
AU - Caramia, Franco
AU - Savas, Peter
AU - Harris, Michael A
AU - Pan, Jia-Wern
AU - Wang, Jianan
AU - Brown, Emmaline
AU - O'Malley, Megan M R
AU - van Geelen, Courtney T
AU - Hun, Michael
AU - Burn, Thomas N
AU - Sant, Sneha
AU - Ballan, Jamieson D
AU - Kay, Jasmine
AU - Lara Gonzalez, Luis E
AU - Clarke, Kylie
AU - Aw Yeang, Han Xian
AU - Idrizi, Rejhan
AU - Jana, Metta
AU - Challice, Damon J
AU - Salgado, Roberto
AU - Thorne, Heather
AU - Poliness, Cathie
AU - Nightingale, Sophie
AU - Teo, Soo-Hwang
AU - Speed, Terence P
AU - Visvader, Jane
AU - Neeson, Paul J
AU - Darcy, Phillip K
AU - Mackay, Laura K
AU - Loi, Sherene
AU - Cohen, Paul
N1 - © 2025. The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2025
Y1 - 2025
N2 - Parity and breastfeeding reduce the risk of breast cancer, particularly triple-negative breast cancer (TNBC)1,2, yet the immunological mechanisms underlying this protection remain unclear. Here, we show that parity induces an accumulation of CD8+ T cells, including cells with a tissue-resident memory (TRM)-like phenotype within human normal breast tissue. In murine models, pregnancy followed by lactation and involution drove the accumulation of CD8⁺ T cells in the mammary gland, coinciding with reduced tumour growth and increased intratumoural immune cell infiltration, effects that were abrogated by CD8⁺ T cell depletion. Importantly, this CD8+ T cell dependent tumour control was only observed following a complete cycle of lactation and involution. Consistent with this, primary TNBCs from parous women exhibited greater T cell infiltration and improved clinical outcomes. Together these findings, spanning preclinical models and over 1000 patient samples, provide new insight into how reproductive history shapes breast immunity, positioning CD8⁺ T cells as key mediators of parity-associated protection and informing novel strategies for both prevention and treatment of breast cancer.
AB - Parity and breastfeeding reduce the risk of breast cancer, particularly triple-negative breast cancer (TNBC)1,2, yet the immunological mechanisms underlying this protection remain unclear. Here, we show that parity induces an accumulation of CD8+ T cells, including cells with a tissue-resident memory (TRM)-like phenotype within human normal breast tissue. In murine models, pregnancy followed by lactation and involution drove the accumulation of CD8⁺ T cells in the mammary gland, coinciding with reduced tumour growth and increased intratumoural immune cell infiltration, effects that were abrogated by CD8⁺ T cell depletion. Importantly, this CD8+ T cell dependent tumour control was only observed following a complete cycle of lactation and involution. Consistent with this, primary TNBCs from parous women exhibited greater T cell infiltration and improved clinical outcomes. Together these findings, spanning preclinical models and over 1000 patient samples, provide new insight into how reproductive history shapes breast immunity, positioning CD8⁺ T cells as key mediators of parity-associated protection and informing novel strategies for both prevention and treatment of breast cancer.
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:001629736000001
U2 - 10.1038/s41586-025-09713-5
DO - 10.1038/s41586-025-09713-5
M3 - Article
C2 - 41115453
SN - 0028-0836
JO - Nature
JF - Nature
ER -