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Macrophages in ovarian cancer and their interactions with monoclonal antibody therapies
Author(s) -
Gabriel Osborn,
Chara Stavraka,
Rebecca Adams,
Ahmad Sayasneh,
Sharmistha Ghosh,
Ana Montes,
Katie E. Lacy,
Rebecca Kristeleit,
James Spicer,
Debra H. Josephs,
James N. Arnold,
Sophia N. Karagiannis
Publication year - 2021
Publication title -
clinical and experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1093/cei/uxab020
Subject(s) - monoclonal antibody , ovarian cancer , immunosuppression , tumor microenvironment , cancer research , cancer , antibody , phenotype , immunology , biology , medicine , tumor cells , biochemistry , gene
The unmet clinical need for effective treatments in ovarian cancer has yet to be addressed using monoclonal antibodies (mAbs), which have largely failed to overcome tumour-associated immunosuppression, restrict cancer growth, and significantly improve survival. In recent years, experimental mAb design has moved away from solely targeting ovarian tumours and instead sought to modulate the wider tumour microenvironment (TME). Tumour-associated macrophages (TAMs) may represent an attractive therapeutic target for mAbs in ovarian cancer due to their high abundance and close proximity to tumour cells and their active involvement in facilitating several pro-tumoural processes. Moreover, the expression of several antibody crystallisable fragment (Fc) receptors and broad phenotypic plasticity of TAMs provide opportunities to modulate TAM polarisation using mAbs to promote anti-tumoural phenotypes. In this review, we discuss the role of TAMs in ovarian cancer TME and the emerging strategies to target the contributions of these cells in tumour progression through the rationale design of mAbs.

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