Recent evidence suggests that host immune cells contribute to the development of malignant pleural effusion (MPE), a common manifestation of metastatic cancer. We have identified such cells, predominantly mononuclear myeloid cells, recruited by tumor-orchestrated inflammatory chemokines. Moreover, targeting of these inflammation-associated mediators modified the disease course of MPE in mice.
Keywords: CCL12; CCL2; adenocarcinoma; angiogenesis; inflammation; malignant pleural effusion; neutralizing antibodies; vascular permeability.